AS3D Human


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Human Gene Lists M
Monogenic Disease Genes1687 genes
membrane, IEA638 genes
Myosin_tail_1, Myosin tail. The myosin molecule is a multi-subunit complex made up of two heavy chains and four light chains it is a fundamental contractile protein found in all eukaryote cell types. This family consists of the coiled-coil myo335 genes
molecular_function unknown, ND324 genes
MAD, Mitotic checkpoint protein. This family consists of several eukaryotic mitotic checkpoint (Mitotic arrest deficient or MAD) proteins. The mitotic spindle checkpoint monitors proper attachment of the bipolar spindle to the kinetochores of 300 genes
metabolism, IEA282 genes
mitochondrion, IEA251 genes
membrane fraction, TAS235 genes
magnesium ion binding, IEA158 genes
membrane fraction, NR151 genes
mitochondrion, TAS105 genes
morphogenesis, TAS97 genes
molecular_function unknown, IEA58 genes
Mito_carr, Mitochondrial carrier protein56 genes
microsome, IEA56 genes
muscle contraction, TAS56 genes
metal ion binding, IEA56 genes
motor activity, IEA54 genes
metalloendopeptidase activity, IEA54 genes
Merozoite_SPAM, Merozoite surface protein (SPAM). This family consists of several Plasmodium falciparum SPAM (secreted polymorphic antigen associated with merozoites) proteins. Variation among SPAM alleles is the result of deletions and amino 47 genes
muscle development, IEA47 genes
mitochondrion, NR46 genes
muscle development, TAS45 genes
mitosis, IEA44 genes
Mpp10, Mpp10 protein. This family includes proteins related to Mpp10 (M phase phosphoprotein 10). The U3 small nucleolar ribonucleoprotein (snoRNP) is required for three cleavage events that generate the mature 18S rRNA from the pre-rRNA. In S43 genes
MAGE, MAGE family. The MAGE (melanoma antigen-encoding gene) family are expressed in a wide variety of tumours but not in normal cells, with the exception of the male germ cells, placenta, and, possibly, cells of the developing embryo. The cel41 genes
manganese ion binding, IEA41 genes
Myosin_head, Myosin head (motor domain)40 genes
MCPVI, Minor capsid protein VI. This minor capsid protein may act as a link between the external capsid and the internal DNA-protein core. The C-terminal 11 residues may function as a protease cofactor leading to enzyme activation40 genes
membrane, NAS39 genes
metallopeptidase activity, IEA37 genes
monooxygenase activity, IEA35 genes
myosin, IEA35 genes
MAP65_ASE1, Microtubule associated protein (MAP65/ASE1 family)34 genes
mRNA processing, IEA34 genes
methyltransferase activity, IEA34 genes
MARVEL, Membrane-associating domain. MARVEL domain-containing proteins are often found in lipid-associating proteins - such as Occludin and MAL family proteins. It may be part of the machinery of membrane apposition events, such as transport v31 genes
Mak16, Mak16 protein. The precise function of this eukaryotic protein family is unknown. The yeast orthologues have been implicated in cell cycle progression and biogenesis of 60S ribosomal subunits. The Schistosoma mansoni Mak16 has been show31 genes
mitochondrial inner membrane, IEA30 genes
microtubule-based movement, IEA30 genes
MSP1_C, Merozoite surface protein 1 (MSP1) C-terminus. This family represents the C-terminal region of merozoite surface protein 1 (MSP1) which are found in a number of Plasmodium species. MSP-1 is a 200-kDa protein expressed on the surface of29 genes
microsome, TAS28 genes
Myb_DNA-binding, Myb-like DNA-binding domain. This family contains the DNA binding domains from Myb proteins, as well as the SANT domain family26 genes
Metallophos, Calcineurin-like phosphoesterase. This family includes a diverse range of phosphoesterases, including protein phosphoserine phosphatases, nucleotidases, sphingomyelin phosphodiesterases and 2'-3' cAMP phosphodiesterases as well as25 genes
MSP4, Merozoite surface protein 4/5 (MSP4/5). This family consists of Merozoite surface proteins 4 and 5 (MSP4/5). MSP4 is a protein with apparent molecular mass of 40 kDa that is synthesised by mature stage parasites and anchored to the meroz25 genes
mitochondrion, ISS25 genes
microtubule associated complex, IEA25 genes
MHC_I, Class I Histocompatibility antigen, domains alpha 1 and 224 genes
mitosis, TAS23 genes
microtubule polymerization, IEA22 genes
MFAP1_C, Micro-fibrillar-associated protein 1 C-terminus. This family represents the C-terminus (approximately 300 residues) of eukaryotic micro-fibrillar-associated protein 1, which is a component of elastin-associated microfibrils in the ext21 genes
metal ion transport, IEA20 genes
MMR_HSR1, GTPase of unknown function19 genes
MAM, MAM domain. An extracellular domain found in many receptors18 genes
membrane, TAS18 genes
mitochondrial electron transport, NADH to ubiquinone, TAS17 genes
meiotic recombination, TAS17 genes
MIP, Major intrinsic protein. MIP (Major Intrinsic Protein) family proteins exhibit essentially two distinct types of channel properties: (1) specific water transport by the aquaporins, and (2) small neutral solutes transport, such as glycerol15 genes
MARCKS, MARCKS family15 genes
MreB_Mbl, MreB/Mbl protein. This family consists of bacterial MreB and Mbl proteins as well as two related archaeal sequences. MreB is known to be a rod shape-determining protein in bacteria and goes to make up the bacterial cytoskeleton. Gene15 genes
microtubule motor activity, NAS15 genes
mRNA processing, TAS15 genes
mesoderm development, TAS15 genes
metal ion transporter activity, IEA15 genes
MATH, MATH domain. This motif has been called the Meprin And TRAF-Homology (MATH) domain. This domain is hugely expanded in the nematode C. elegans14 genes
Mov34, Mov34/MPN/PAD-1 family. Members of this family are found in proteasome regulatory subunits, eukaryotic initiation factor 3 (eIF3) subunits and regulators of transcription factors. This family is also known as the MPN domain and PAD-1-li14 genes
Myosin_N, Myosin N-terminal SH3-like domain. This domain has an SH3-like fold. It is found at the N-terminus of many but not all myosins. The function of this domain is unknown14 genes
Myotub-related, Myotubularin-related. This family represents a region within eukaryotic myotubularin-related proteins that is sometimes found with pfam02893. Myotubularin is a dual-specific lipid phosphatase that dephosphorylates phosphatidyli14 genes
microtubule associated complex, TAS14 genes
mitochondrion, NAS13 genes
membrane fusion, TAS13 genes
MIF4G, MIF4G domain. MIF4G is named after Middle domain of eukaryotic initiation factor 4G (eIF4G). Also occurs in NMD2p and CBP80. The domain is rich in alpha-helices and may contain multiple alpha-helical repeats. In eIF4G, this domain binds12 genes
MH1, MH1 domain. This is the MH1 (MAD homology 1) domain found at the amino terminus of MAD related proteins. This domain can bind to DNA. This domain is separated from the MH2 domain by a non-conserved linker region. The crystal structure of 12 genes
microtubule motor activity, IEA12 genes
membrane alanyl aminopeptidase activity, IEA12 genes
microsome, NAS12 genes
muscle myosin, TAS12 genes
meiosis, IEA12 genes
male gonad development, TAS12 genes
Myc_N, Myc amino-terminal region. The myc family belongs to the basic helix-loop-helix leucine zipper class of transcription factors, see pfam00010. Myc forms a heterodimer with Max, and this complex regulates cell growth through direct activa11 genes
Menin, Menin. MEN1, the gene responsible for multiple endocrine neoplasia type 1, is a tumour suppressor gene that encodes a protein called Menin which may be an atypical GTPase stimulated by nm2311 genes
membrane fraction, IDA11 genes
metabolism, TAS11 genes
MACPF, MAC/Perforin domain. The membrane-attack complex (MAC) of the complement system forms transmembrane channels. These channels disrupt the phospholipid bilayer of target cells, leading to cell lysis and death. A number of proteins partici10 genes
MBOAT, MBOAT family. The MBOAT (membrane bound O-acyl transferase) family of membrane proteins contains a variety of acyltransferase enzymes. A conserved histidine has been suggested to be the active site residue10 genes
microtubule motor activity, TAS10 genes
mitochondrion, IDA10 genes
mitochondrial inner membrane, TAS10 genes
mismatch repair, TAS10 genes
mRNA-nucleus export, IEA10 genes
mitochondrial transport, IEA10 genes
muscle contraction, NR10 genes
membrane, NR10 genes
MAP kinase phosphatase activity, IEA10 genes
MCM, MCM2/3/5 family9 genes
MHC_II_beta, Class II histocompatibility antigen, beta domain9 genes
MBD, Methyl-CpG binding domain. The Methyl-CpG binding domain (MBD) binds to DNA that contains one or more symmetrically methylated CpGs. DNA methylation in animals is associated with alterations in chromatin structure and silencing of gene ex9 genes
MIR, MIR domain. The MIR (protein mannosyltransferase, IP3R and RyR) domain is a small domain that may have a ligand transferase function9 genes
MBT, mbt repeat. The function of this repeat is unknown, but is found in a number of nuclear proteins such as drosophila sex comb on midleg protein. The repeat is found in up to four copies. The repeat contains a completely conserved glutamate9 genes
MAP1_LC3, Microtubule associated protein 1A/1B, light chain 3. Light chain 3 is proposed to function primarily as a subunit of microtubule associated proteins 1A and 1B and that its expression may regulate microtubule binding activity9 genes
MIT, MIT domain9 genes
MSF1, MSF1-like conserved region. This family includes a conserved region found in the yeast YLR168C gene MSF1 product. The function of this protein is unknown, though it is thought to be involved in intra-mitochondrial protein sorting. This r9 genes
Myosin_tail_2, Myosin tail9 genes
mediator complex, IDA9 genes
motor activity, TAS9 genes
metalloendopeptidase activity, TAS9 genes
MAP kinase activity, IEA9 genes
metabotropic glutamate, GABA-B-like receptor activity, IEA9 genes
Met_10, Met-10+ like-protein. The methionine-10 mutant allele of N. crassa codes for a protein of unknown function. However, homologous proteins have been found in yeast suggesting this protein may be involved in methionine biosynthesis, trans8 genes
MH2, MH2 domain. This is the MH2 (MAD homology 2) domain found at the carboxy terminus of MAD related proteins. This domain is separated from the MH1 domain by a non-conserved linker region. The MH2 domain mediates interaction with a wide vari8 genes
microfilament motor activity, NAS8 genes
MAPKKK cascade, TAS8 genes
MAP kinase kinase activity, TAS8 genes
membrane fraction, ISS8 genes
membrane fraction, NAS8 genes
mitochondrial matrix, NAS8 genes
mitochondrial matrix, TAS8 genes
microsome, NR8 genes
meiosis, TAS8 genes
metabotropic glutamate, GABA-B-like receptor activity, TAS8 genes
morphogenesis, NR8 genes
MCPsignal, Methyl-accepting chemotaxis protein (MCP) signaling domain. This domain is thought to transduce the signal to CheA since it is highly conserved in very diverse MCPs7 genes
MyTH4, MyTH4 domain. Domain in myosin and kinesin tails, present twice in myosin-VIIa, and also present in 3 other myosins7 genes
Mucin, Mucin-like glycoprotein. This family of trypanosomal proteins resemble vertebrate mucins. The protein consists of three regions. The N and C terminii are conserved between all members of the family, whereas the central region is not wel7 genes
MA3, MA3 domain. Domain in DAP-5, eIF4G, MA-3 and other proteins. Highly alpha-helical. May contain repeats and/or regions similar to MIF4G domains7 genes
Mab-21, Mab-21 protein7 genes
Mob1_phocein, Mob1/phocein family. Mob1 is an essential Saccharomyces cerevisiae protein, identified from a two-hybrid screen, that binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. Mo7 genes
mitochondrial outer membrane, NAS7 genes
mitochondrial outer membrane, TAS7 genes
mitochondrial inner membrane presequence translocase complex, TAS7 genes
mitochondrial small ribosomal subunit, IDA7 genes
mitosis, NAS7 genes
muscle development, NAS7 genes
MHC class I receptor activity, NAS7 genes
muscle fiber, IEA7 genes
MHC_II_alpha, Class II histocompatibility antigen, alpha domain6 genes
MAPEG, MAPEG family. This family is has been called MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism). It includes proteins such as Prostaglandin E synthase. This enzyme catalyses the synthesis of PGE2 from PGH2 (pr6 genes
MOZ_SAS, MOZ/SAS family. This region of these proteins has been suggested to be homologous to acetyltransferases6 genes
MutS_III, MutS domain III. This domain is found in proteins of the MutS family (DNA mismatch repair proteins) and is found associated with pfam00488, pfam05188, pfam01624 and pfam05190. The MutS family of proteins is named after the Salmonella6 genes
MRG, MRG. This family consists of three different eukaryotic proteins (mortality factor 4 (MORF4/MRG15), male-specific lethal 3(MSL-3) and ESA1-associated factor 3(EAF3)). It is thought that the MRG family is involved in transcriptional regula6 genes
MAT1, CDK-activating kinase assembly factor MAT1. MAT1 is an assembly/targeting factor for cyclin-dependent kinase-activating kinase (CAK), which interacts with the transcription factor TFIIH. The domain found to the N-terminal side of this do6 genes
Mod_r, Modifier of rudimentary (Mod(r)) protein. This family represents a conserved region approximately 150 residues long within a number of eukaryotic proteins that show homology with Drosophila melanogaster Modifier of rudimentary (Mod(r)) 6 genes
mitotic sister chromatid segregation, TAS6 genes
mRNA binding, TAS6 genes
mitochondrial membrane, TAS6 genes
mitochondrial outer membrane, IEA6 genes
mitochondrial inner membrane, NAS6 genes
mitochondrial inner membrane, NR6 genes
mitochondrial electron transport chain, IEA6 genes
mitochondrial matrix, NR6 genes
microtubule, IEA6 genes
mRNA splice site selection, TAS6 genes
microtubule-based movement, NAS6 genes
metalloexopeptidase activity, IEA6 genes
MHC class II receptor activity, IEA6 genes
MutS_V, MutS domain V. This domain is found in proteins of the MutS family (DNA mismatch repair proteins) and is found associated with pfam01624, pfam05188, pfam05192 and pfam05190. The mutS family of proteins is named after the Salmonella typ5 genes
Motile_Sperm, MSP (Major sperm protein) domain. Major sperm proteins are involved in sperm motility. These proteins oligomerise to form filaments. This family contains many other proteins5 genes
Mtc, Tricarboxylate carrier5 genes
MIB_HERC2, Mib_herc2. Named "mib/herc2 domain" in. Usually the protein also contains an E3 ligase domain (either Ring or Hect)5 genes
magnesium ion binding, IDA5 genes
magnesium ion binding, NAS5 genes
monooxygenase activity, NAS5 genes
monooxygenase activity, TAS5 genes
mannosyl-oligosaccharide 1,2-alpha-mannosidase activity, IEA5 genes
MAP kinase activity, TAS5 genes
muscarinic acetylcholine receptor activity, TAS5 genes
mannose binding, TAS5 genes
membrane attack complex, IEA5 genes
mitochondrial electron transport chain, TAS5 genes
mitochondrial small ribosomal subunit, NAS5 genes
microsome, ISS5 genes
mRNA polyadenylation, TAS5 genes
mitotic spindle assembly, TAS5 genes
myogenesis, TAS5 genes
microtubule binding, IDA5 genes
microtubule binding, TAS5 genes
monocarboxylic acid transporter activity, TAS5 genes
monocarboxylate porter activity, IEA5 genes
microtubule cytoskeleton, TAS5 genes
monocarboxylic acid transport, TAS5 genes
membrane coat adaptor complex, TAS5 genes
MHC class II receptor activity, TAS5 genes
malic, Malic enzyme, N-terminal domain4 genes
MAS20, MAS20 protein import receptor4 genes
mTERF, mTERF. This family contains one sequence of known function Human mitochondrial transcription termination factor (mTERF) the rest of the family consists of hypothetical proteins none of which have any functional information. mTERF is a m4 genes
MutS_II, MutS domain II. This domain is found in proteins of the MutS family (DNA mismatch repair proteins) and is found associated with pfam00488, pfam01624, pfam05192 and pfam05190. The MutS family of proteins is named after the Salmonella t4 genes
MutS_IV, MutS family domain IV. This domain is found in proteins of the MutS family (DNA mismatch repair proteins) and is found associated with pfam01624, pfam05188, pfam05192 and pfam00488. The mutS family of proteins is named after the Salmo4 genes
MGC-24, Multi-glycosylated core protein 24 (MGC-24). This family consists of several MGC-24 (or Cd164 antigen) proteins from eukaryotic organisms. MGC-24/CD164 is a sialomucin expressed in many normal and cancerous tissues. In humans, soluble 4 genes
Mesothelin, Pre-pro-megakaryocyte potentiating factor precursor (Mesothelin). This family consists of several mammalian pre-pro-megakaryocyte potentiating factor precursor (MPF) or mesothelin proteins. Mesothelin is a glycosylphosphatidylinosi4 genes
microfilament motor activity, TAS4 genes
MAPKKK cascade, ISS4 genes
microtubule cytoskeleton organization and biogenesis, IEA4 genes
mRNA binding, NAS4 genes
mRNA 3'-UTR binding, TAS4 genes
metalloendopeptidase activity, NAS4 genes
monooxygenase activity, ISS4 genes
mannosyl-oligosaccharide 1,2-alpha-mannosidase activity, TAS4 genes
MAP kinase kinase kinase activity, TAS4 genes
mitochondrial membrane, IEA4 genes
mitochondrial inner membrane presequence translocase complex, IEA4 genes
muscle thin filament tropomyosin, TAS4 genes
mismatch repair, IEA4 genes
mRNA-nucleus export, IDA4 genes
melanin biosynthesis from tyrosine, IEA4 genes
Mo-molybdopterin cofactor biosynthesis, IEA4 genes
mitosis, NR4 genes
mitotic chromosome condensation, IEA4 genes
mitotic checkpoint, TAS4 genes
mechanosensory behavior, IEA4 genes
microtubule binding, IEA4 genes
metallopeptidase activity, TAS4 genes
monovalent inorganic cation transporter activity, IEA4 genes
membrane, IDA4 genes
membrane, ISS4 genes
mRNA metabolism, NAS4 genes
MHC class I receptor activity, TAS4 genes
MHC class II receptor activity, NAS4 genes
MIF, Macrophage migration inhibitory factor (MIF)3 genes
Myelin_PLP, Myelin proteolipid protein (PLP or lipophilin)3 genes
Monooxygenase, Monooxygenase. This family includes diverse enzymes that utilise FAD3 genes
MutS_I, MutS domain I. This domain is found in proteins of the MutS family (DNA mismatch repair proteins) and is found associated with pfam00488, pfam05188, pfam05192 and pfam05190. The MutS family of proteins is named after the Salmonella typ3 genes
MgtE, Divalent cation transporter. This region is the integral membrane part of the eubacterial MgtE family of magnesium transporters. Related regions are found also in archaebacterial and eukaryotic proteins. All the archaebacterial and eukar3 genes
Melibiase, Melibiase3 genes
MGS, MGS-like domain. This domain composes the whole protein of methylglyoxal synthetase and the domain is also found in Carbamoyl phosphate synthetase (CPS) where it forms a regulatory domain that binds to the allosteric effector ornithine. T3 genes
MORN, MORN repeat. The MORN (Membrane Occupation and Recognition Nexus) repeat is found in multiple copies in several proteins including junctophilins (See Takeshima et al. Mol. Cell 2000;6:11-22). The function of this motif is unknown3 genes
MOSC, MOSC domain. The MOSC (MOCO sulfurase C-terminal) domain is a superfamily of beta-strand-rich domains identified in the molybdenum cofactor sulfurase and several other proteins from both prokaryotes and eukaryotes. These MOSC domains con3 genes
MOSC_N, MOSC N-terminal beta barrel domain. This domain is found to the N-terminus of pfam03473. The function of this domain is unknown, however it is predicted to adopt a beta barrel fold3 genes
Mtp, Golgi 4-transmembrane spanning transporter3 genes
Malic_M, Malic enzyme, NAD binding domain3 genes
Mpv17_PMP22, Mpv17 / PMP22 family. The 22-kDa peroxisomal membrane protein (PMP22) is a major component of peroxisomal membranes. PMP22 seems to be involved in pore forming activity and may contribute to the unspecific permeability of the orga3 genes
MT-A70, MT-A70. MT-A70 is the S-adenosylmethionine-binding subunit of human mRNA:m6A methyl-transferase (MTase), an enzyme that sequence-specifically methylates adenines in pre-mRNAs3 genes
M-inducer_phosp, M-phase inducer phosphatase. This family represents a region within eukaryotic M-phase inducer phosphatases (EC:3.1.3.48), which also contain the pfam00581 domain. These proteins are involved in the control of mitosis3 genes
MHC_I_C, MHC_I C-terminus. This family represents the C-terminal region of the MHC class I antigen. The family is found in conjunction with pfam00129 and pfam000473 genes
mitotic anaphase, TAS3 genes
MAPKKK cascade, NAS3 genes
mRNA catabolism, nonsense-mediated, NAS3 genes
microtubule cytoskeleton organization and biogenesis, TAS3 genes
membrane dipeptidase activity, IEA3 genes
methionyl aminopeptidase activity, IEA3 genes
melanocortin receptor activity, TAS3 genes
membrane fraction, IEP3 genes
mitochondrial outer membrane, IDA3 genes
mitochondrial ribosome, NAS3 genes
mitochondrial large ribosomal subunit, NAS3 genes
muscle myosin, NR3 genes
microtubule, NAS3 genes
microtubule, TAS3 genes
mismatch repair, NAS3 genes
mitotic recombination, TAS3 genes
mRNA cleavage, TAS3 genes
mRNA catabolism, TAS3 genes
mRNA-nucleus export, TAS3 genes
membrane protein ectodomain proteolysis, IDA3 genes
mitochondrion organization and biogenesis, ISS3 genes
microtubule-based process, IEA3 genes
microtubule-based process, NAS3 genes
microtubule-based movement, TAS3 genes
microtubule stabilization, IEA3 genes
mitotic spindle checkpoint, TAS3 genes
muscarinic acetylcholine receptor, phospholipase C activating pathway, TAS3 genes
muscle development, NR3 genes
myogenesis, IEA3 genes
myoblast fusion, TAS3 genes
microtubule binding, ISS3 genes
metabolism, NAS3 genes
metallopeptidase activity, NR3 genes
MP kinase activity, IDA3 genes
methionine biosynthesis, IEA3 genes
myosin, NAS3 genes
molybdenum ion binding, IEA3 genes
melanin-concentrating hormone activity, IEA3 genes
MHC class I protein binding, ISS3 genes
MHC class I protein binding, NAS3 genes
metal ion binding, NAS3 genes
metal ion binding, TAS3 genes
Methyltransf_2, O-methyltransferase. This family includes a range of O-methyltransferases. These enzymes utilise S-adenosyl methionine2 genes
Mtap_PNP, Phosphorylase family 22 genes
MoCF_biosynth, Probable molybdopterin binding domain. This domain is found a variety of proteins involved in biosynthesis of molybdopterin cofactor. The domain is presumed to bind molybdopterin. The structure of this domain is known, and it fo2 genes
MatE, MatE. The MatE domain2 genes
Methyltransf_3, O-methyltransferase. Members of this family are O-methyltransferases. The family includes catechol o-methyltransferase, caffeoyl-CoA O-methyltransferase and a family of bacterial O-methyltransferases that may be involved in ant2 genes
Methyltransf_5, MraW methylase family. Members of this family are probably SAM dependent methyltransferases. This family appears to be related to pfam015962 genes
Man-6-P_recep, Cation-dependent mannose-6-phosphate receptor2 genes
Methyltransf_4, Putative methyltransferase. This is a family of putative methyltransferases. The aligned region contains the GXGXG S-AdoMet binding site suggesting a putative methyltransferase activity2 genes
Mago_nashi, Mago nashi protein. This family was originally identified in Drosophila and called mago nashi, it is a strict maternal effect, grandchildless-like, gene. The human homologue has been shown to interact with an RNA binding protein. A2 genes
Mo25, Mo25 protein family2 genes
Mnd1, Mnd1 family. This family of proteins includes MND1 from S. cerevisiae. The mnd1 protein forms a complex with hop2 to promote homologous chromosome pairing and meiotic double-strand break repair2 genes
Motilin_assoc, Motilin/ghrelin-associated peptide. This family represents a peptide sequence that lies C-terminal to motilin/ghrelin on the respective precursor peptide. Its function is unknown2 genes
MOBP, Myelin-associated oligodendrocytic basic protein (MOBP). MOBP is abundantly expressed in central nervous system myelin, and shares several characteristics with myelin basic protein (MBP), in terms of regional distribution and function. M2 genes
Methyltransf_8, Hypothetical methyltransferase. This family consists of several uncharacterised eukaryotic proteins which are related to methyltransferases pfam012092 genes
MAGP, Microfibril-associated glycoprotein (MAGP). This family consists of several mammalian microfibril-associated glycoprotein (MAGP) 1 and 2 proteins. MAGP1 and 2 are components of elastic fibres. MAGP-1 has been proposed to bind a C-termina2 genes
MRVI1, MRVI1 protein. This family consists of mammalian MRVI1 proteins which are related to the lymphoid-restricted membrane protein (JAW1) and the IP3 receptor associated cGMP kinase substrates A and B (IRAGA and IRAGB). The function of MRVI12 genes
MCLC, Mid-1-related chloride channel (MCLC). This family consists of several mid-1-related chloride channels. mid-1-related chloride channel (MCLC) proteins function as a chloride channel when incorporated in the planar lipid bilayer2 genes
Mast_C, Mast C-terminus. This family represents the C-terminus (approximately 150 residues) of Mast, a microtubule-associated protein. It has been suggested that Mast plays an essential role in centrosome separation and organisation of the bip2 genes
mitotic spindle elongation, TAS2 genes
M phase of mitotic cell cycle, IEA2 genes
M phase of mitotic cell cycle, TAS2 genes
mediator complex, NAS2 genes
meiotic spindle assembly, ISS2 genes
mitotic cell cycle, IEA2 genes
magnesium ion binding, ISS2 genes
microfibril, IEA2 genes
mRNA 3'-UTR binding, NR2 genes
methylated-DNA-[protein]-cysteine S-methyltransferase activity, IEA2 genes
macrophage elastase activity, TAS2 genes
malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) activity, TAS2 genes
methenyltetrahydrofolate cyclohydrolase activity, TAS2 genes
methionine adenosyltransferase activity, TAS2 genes
methylcrotonoyl-CoA carboxylase activity, NAS2 genes
macrophage colony stimulating factor receptor activity, TAS2 genes
molecular_function unknown, NAS2 genes
mitochondrion, IEP2 genes
mitochondrial outer membrane, NR2 genes
mitochondrial matrix, IDA2 genes
mitochondrial matrix, IEA2 genes
mitochondrial large ribosomal subunit, TAS2 genes
muscle myosin, NAS2 genes
microtubule, IDA2 genes
microtubule associated complex, NAS2 genes
microvillus, NR2 genes
malate metabolism, IEA2 genes
mitochondrial electron transport, NADH to ubiquinone, IEA2 genes
mitochondrial electron transport, ubiquinol to cytochrome c, IEA2 genes
mutagenesis, TAS2 genes
mRNA capping, TAS2 genes
mRNA cleavage, NAS2 genes
mRNA editing, TAS2 genes
mRNA-nucleus export, NAS2 genes
methionyl-tRNA aminoacylation, IEA2 genes
membrane protein ectodomain proteolysis, ISS2 genes
methionine metabolism, TAS2 genes
melanin biosynthesis from tyrosine, TAS2 genes
membrane lipid metabolism, TAS2 genes
mitochondrial transport, TAS2 genes
multidrug transport, IEA2 genes
metal ion homeostasis, TAS2 genes
muscle contraction, NAS2 genes
microtubule-based process, ISS2 genes
microtubule nucleation, IDA2 genes
microtubule nucleation, ISS2 genes
microtubule nucleation, NAS2 genes
microtubule stabilization, NAS2 genes
mitotic spindle assembly, ISS2 genes
mitotic checkpoint, IDA2 genes
mesoderm development, NAS2 genes
mesoderm cell fate determination, TAS2 genes
muscle development, ISS2 genes
myoblast cell fate determination, TAS2 genes
microtubule binding, NAS2 genes
metalloendopeptidase inhibitor activity, NAS2 genes
metalloendopeptidase inhibitor activity, NR2 genes
metalloendopeptidase inhibitor activity, TAS2 genes
metallopeptidase activity, IDA2 genes
metallopeptidase activity, NAS2 genes
methyl-CpG binding, NAS2 genes
melatonin receptor activity, TAS2 genes
monoamine transporter activity, TAS2 genes
morphogenesis, NAS2 genes
microtubule cytoskeleton, ISS2 genes
microtubule cytoskeleton, NAS2 genes
monoamine transport, TAS2 genes
membrane organization and biogenesis, ISS2 genes
MHC class I receptor activity, IEA2 genes
manganese ion binding, NAS2 genes
mitochondrial matrix protein import, NAS2 genes
male genital morphogenesis, TAS2 genes
macrophage activation, NAS2 genes
MHC class I protein binding, IEP2 genes
myelination, ISS2 genes
MHC class II receptor activity, NR2 genes
muscle maintenance, ISS2 genes
metal ion binding, NR2 genes
macrophage chemotaxis, IDA2 genes
Molybdopterin, Molybdopterin oxidoreductase1 genes
Methyltransf_1, 6-O-methylguanine DNA methyltransferase, DNA binding domain. This domain is a 3 helical bundle1 genes
MR_MLE, Mandelate racemase / muconate lactonizing enzyme, C-terminal domain. C-terminal domain is TIM barrel fold, dehydratase-like domain. Manganese is associated with this domain1 genes
mRNA_cap_enzyme, mRNA capping enzyme, catalytic domain. This family represents the ATP binding catalytic domain of the mRNA capping enzyme1 genes
MaoC_dehydratas, MaoC like domain. The MaoC protein is found to share similarity with a wide variety of enzymes; estradiol 17 beta-dehydrogenase 4, peroxisomal hydratase-dehydrogenase-epimerase, fatty acid synthase beta subunit. All these enzy1 genes
MM_CoA_mutase, Methylmalonyl-CoA mutase. The enzyme methylmalonyl-CoA mutase is a member of a class of enzymes that uses coenzyme B12 (adenosylcobalamin) as a cofactor. The enzyme induces the formation of an adenosyl radical from the cofactor.1 genes
Myelin_MBP, Myelin basic protein1 genes
Metalloenzyme, Metalloenzyme superfamily. This family includes phosphopentomutase and 2,3-bisphosphoglycerate-independent phosphoglycerate mutase. This family is also related to pfam00245. The alignment contains the most conserved residues tha1 genes
MoaC, MoaC family. Members of this family are involved in molybdenum cofactor biosynthesis. However their molecular function is not known1 genes
Metallothio_PEC, Plant PEC family metallothionein1 genes
Marek_A, Marek's disease glycoprotein A1 genes
MTHFR, Methylenetetrahydrofolate reductase. This family includes the 5,10-methylenetetrahydrofolate reductase EC:1.7.99.5 from bacteria and methylenetetrahydrofolate reductase EC: 1.5.1.20 from eukaryotes. The structure for this domain is know1 genes
MAM33, Mitochondrial glycoprotein. This mitochondrial matrix protein family contains members of the MAM33 family which bind to the globular 'heads' of C1Q. It is thought to be involved in mitochondrial oxidative phosphorylation and in nucleus-1 genes
Myc-LZ, Myc leucine zipper domain. This family consists of the leucine zipper dimerisation domain found in both cellular c-Myc proto-oncogenes and viral v-Myc oncogenes. Dimerisation via the leucine zipper motif with other basic helix-loop-hel1 genes
MoaE, MoaE protein. This family contains the MoaE protein that is involved in biosynthesis of molybdopterin. Molybdopterin, the universal component of the pterin molybdenum cofactors, contains a dithiolene group serving to bind Mo. Addition of1 genes
Maf, Maf-like protein. Maf is a putative inhibitor of septum formation in eukaryotes, bacteria, and archaea1 genes
MR_MLE_N, Mandelate racemase / muconate lactonizing enzyme, N-terminal domain. SCOP reports fold similarity with enolase N-terminal domain1 genes
Methyltransf_1N, 6-O-methylguanine DNA methyltransferase, ribonuclease-like domain1 genes
Met_synt_B12, Vitamin B12 dependent methionine synthase, activation domain1 genes
MVIN, MviN-like protein. Deletion of the mviN virulence gene in Salmonella enterica serovar. Typhimurium greatly reduces virulence in a mouse model of typhoid-like disease. Open reading frames encoding homologues of MviN have since been identi1 genes
MtN3_slv, MtN3/saliva family. This family includes proteins such as drosophila saliva, MtN3 involved in root nodule development and a protein involved in activation and expression of recombination activation genes (RAGs). Although the molecula1 genes
Mo-co_dimer, Mo-co oxidoreductase dimerisation domain. This domain is found in molybdopterin cofactor (Mo-co) oxidoreductases. It is involved in dimer formation, and has an Ig-fold structure1 genes
MoeA_N, MoeA N-terminal region (domain I and II). This family contains two structural domains. One of these contains the conserved DGXA motif. This region is found in proteins involved in biosynthesis of molybdopterin cofactor however the exac1 genes
MoeA_C, MoeA C-terminal region (domain IV). This domain is found in proteins involved in biosynthesis of molybdopterin cofactor however the exact molecular function of this domain is uncertain. The structure of this domain is known and forms a1 genes
Macscav_rec, Macrophage scavenger receptor1 genes
Mra1, Suppressor Mra1. The suppressor Mra1 is found in high-copy-number when Ras1 is mutated, that recovers the mating deficiency caused by the decrease of Ras1 activity. Mutational analysis in yeast suggests that the suppressor Mra1 is essent1 genes
mRNA_cap_C, mRNA capping enzyme, C-terminal domain1 genes
MmgE_PrpD, MmgE/PrpD family. This family includes 2-methylcitrate dehydratase EC:4.2.1.79 (PrpD) that is required for propionate catabolism. It catalyses the third step of the 2-methylcitric acid cycle1 genes
MreD, rod shape-determining protein MreD. MreD (murein formation D) is involved in the rod shape determination in E. coli, and more generally in cell shape determination of bacteria whether or not they are rod-shaped1 genes
Mak10, Mak10 subunit, NatC N(alpha)-terminal acetyltransferase. NatC N(alpha)-terminal acetyltransferases contains Mak10p, Mak31p and Mak3p subunits. All three subunits are associated with each other to form the active complex1 genes
Mre11_DNA_bind, Mre11 DNA-binding presumed domain. The Mre11 complex is a multi-subunit nuclease that is composed of Mre11, Rad50 and Nbs1/Xrs2, and is involved in checkpoint signalling and DNA replication. Mre11 has an intrinsic DNA-binding a1 genes
Mss4, Mss4 protein1 genes
Mog1, Ran-interacting Mob1 protein. Segregation of nuclear and cytoplasmic processes facilitates regulation of many eukaryotic cellular functions such as gene expression and cell cycle progression. Trafficking through the nuclear pore requires1 genes
Motilin_ghrelin, Motilin/ghrelin. Motilin is a gastrointestinal regulatory polypeptide produced by motilin cells in the duodenal epithelium. It is released into the general circulation at about 100-min intervals during the inter-digestive stat1 genes
MED6, MED6 mediator sub complex component. Component of RNA polymerase II holoenzyme and mediator sub complex1 genes
Mannosyl_trans, Mannosyltransferase (PIG-M). PIG-M has a DXD motif. The DXD motif is found in many glycosyltransferases that utilise nucleotide sugars. It is thought that the motif is involved in the binding of a manganese ion that is required1 genes
MGAT2, N-acetylglucosaminyltransferase II (MGAT2). UDP-N-acetyl-D-glucosamine:alpha-6-D-mannoside beta-1,2-N- acetylglucosaminyltransferase II (EC 2.4.1.143) (GnT II/MGAT2) is a Golgi resident enzyme that catalyses an essential step in the bio1 genes
MOFRL, MOFRL family. MOFRL(multi-organism fragment with rich Leucine) family exists in bacteria and eukaryotes. The function of this domain is not clear, although it exists in some putative enzymes such as reductases and kinases1 genes
MPPN, MPPN (rrm-like) domain. The MPPN (Mitotic PhosphoProtein N' end) family is uncharacterised however it probably plays a role in the cell cycle because the family includes mitotic phosphoproteins. This family also includes a suppressor of 1 genes
MoeZ_MoeB, MoeZ/MoeB domain. This putative domain is found in the MoeZ protein and the MoeB protein. The domain has two CXXC motifs that are only partly conserved1 genes
MCD, Malonyl-CoA decarboxylase (MCD). This family consists of several eukaryotic malonyl-CoA decarboxylase (MLYCD) proteins. Malonyl-CoA, in addition to being an intermediate in the de novo synthesis of fatty acids, is an inhibitor of carnitin1 genes
Mt_ATP-synt_B, Mitochondrial ATP synthase B chain precursor (ATP-synt_B). The Fo sector of the ATP synthase is a membrane bound complex which mediates proton transport. It is composed of nine different polypeptide subunits (a, b, c, d, e, f, g1 genes
Mis12, Mis12 protein. Kinetochores are the chromosomal sites for spindle interaction and play a vital role for chromosome segregation. Fission yeast kinetochore protein Mis12, is required for correct spindle morphogenesis, determining metaphas1 genes
Mt_ATP-synt_D, ATP synthase D chain, mitochondrial (ATP5H). This family consists of several ATP synthase D chain, mitochondrial (ATP5H) proteins. Subunit d has no extensive hydrophobic sequences, and is not apparently related to any subunit de1 genes
MED7, MED7 protein. This family consists of several eukaryotic proteins which are homologues of the yeast MED7 protein. Activation of gene transcription in metazoans is a multistep process that is triggered by factors that recognise transcript1 genes
Mob_synth_C, Molybdenum Cofactor Synthesis C. This region contains two iron-sulphur (3Fe-4S) binding sites. Mutations in this region of human MOCS1A cause MOCOD (Molybdenum Co-Factor Deficiency) type A1 genes
Muskelin_N, Muskelin N-terminus. This family represents the N-terminal region of muskelin and is found in conjunction with several pfam01344 repeats. Muskelin is an intracellular, kelch repeat protein that is needed in cell-spreading responses1 genes
MMS19_N, MMS19 N-terminus. This family represents the N-terminus of the eukaryotic repair/transcription protein MMS19. MMS19 is involved in excision repair of DNA damaged by UV radiation and by other agents that distort the DNA helix, as well 1 genes
MEA1, Male enhanced antigen 1 (MEA1). This family consists of several mammalian male enhanced antigen 1 (MEA1) proteins. The Mea-1 gene is found to be localised in primary and secondary spermatocytes and spermatids, but the protein products ar1 genes
MRP-L47, Mitochondrial 39-S ribosomal protein L47 (MRP-L47). This family represents the N-terminal region (approximately 8 residues) of the eukaryotic mitochondrial 39-S ribosomal protein L47 (MRP-L47). Mitochondrial ribosomal proteins (MRPs) 1 genes
Mic1, Colon cancer-associated protein Mic1-like. This family represents the C-terminus (approximately 160 residues) of a number of proteins that resemble colon cancer-associated protein Mic11 genes
mitochondrial genome maintenance, TAS1 genes
mannosyltransferase activity, IEA1 genes
mitochondrial ornithine transport, NAS1 genes
mitochondrial ornithine transport, TAS1 genes
mitotic sister chromatid segregation, IMP1 genes
mitotic sister chromatid segregation, NAS1 genes
M phase specific microtubule process, TAS1 genes
mediator complex, IEA1 genes
mediator complex, IEP1 genes
mediator complex, NR1 genes
microfilament motor activity, NR1 genes
mitochondrial fission, TAS1 genes
mitotic cell cycle, IDA1 genes
M phase, NAS1 genes
magnesium ion binding, TAS1 genes
microfibril, NAS1 genes
microtubule bundle formation, IEP1 genes
microglial cell activation, IEP1 genes
morphogenesis of an epithelial sheet, ISS1 genes
mRNA 3'-UTR binding, IDA1 genes
motor activity, ISS1 genes
motor activity, NAS1 genes
motor activity, NR1 genes
microtubule motor activity, ISS1 genes
metallocarboxypeptidase activity, TAS1 genes
metalloendopeptidase activity, IDA1 genes
metalloendopeptidase activity, ISS1 genes
matrilysin activity, IEA1 genes
membrane dipeptidase activity, TAS1 genes
meprin A activity, IEA1 genes
meprin A activity, TAS1 genes
methionyl aminopeptidase activity, NAS1 genes
methionyl aminopeptidase activity, TAS1 genes
mitochondrial processing peptidase activity, IEA1 genes
mitochondrial intermediate peptidase activity, IEA1 genes
malic enzyme activity, TAS1 genes
malate dehydrogenase (decarboxylating) activity, TAS1 genes
mannose-6-phosphate isomerase activity, IEA1 genes
mannose-6-phosphate isomerase activity, TAS1 genes
methenyltetrahydrofolate cyclohydrolase activity, IEA1 genes
methionyl-tRNA formyltransferase activity, IEA1 genes
mRNA (guanine-N7-)-methyltransferase activity, TAS1 genes
mRNA guanylyltransferase activity, TAS1 genes
methylenetetrahydrofolate dehydrogenase (NAD+) activity, IEA1 genes
methylenetetrahydrofolate dehydrogenase (NADP+) activity, IEA1 genes
methylenetetrahydrofolate reductase (NADPH) activity, IEA1 genes
methylenetetrahydrofolate reductase (NADPH) activity, TAS1 genes
methylglutaconyl-CoA hydratase activity, IEA1 genes
methylmalonate-semialdehyde dehydrogenase (acylating) activity, NAS1 genes
methylmalonyl-CoA decarboxylase activity, TAS1 genes
methylmalonyl-CoA epimerase activity, NAS1 genes
methylmalonyl-CoA mutase activity, TAS1 genes
mevalonate kinase activity, TAS1 genes
monooxygenase activity, NR1 genes
monophenol monooxygenase activity, IEA1 genes
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase activity, NAS1 genes
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase activity, TAS1 genes
mannosyl-oligosaccharide glucosidase activity, IEA1 genes
myosin-light-chain kinase activity, TAS1 genes
MAP kinase activity, IDA1 genes
MAP kinase activity, ISS1 genes
MAP kinase activity, NAS1 genes
MAP kinase kinase activity, NAS1 genes
MAP kinase kinase kinase activity, IDA1 genes
MAP kinase kinase kinase activity, ISS1 genes
MAP kinase kinase kinase activity, NAS1 genes
methionine-tRNA ligase activity, IEA1 genes
methionine-tRNA ligase activity, TAS1 genes
melanocortin receptor activity, IEA1 genes
melanocyte stimulating hormone receptor activity, IEA1 genes
muscarinic acetylcholine receptor activity, NR1 genes
mu-opioid receptor activity, IEA1 genes
mu-opioid receptor activity, TAS1 genes
MAP-kinase scaffold activity, IPI1 genes
MAP-kinase scaffold activity, ISS1 genes
MAP-kinase scaffold activity, NAS1 genes
macrophage colony stimulating factor receptor binding, TAS1 genes
myo-inositol:sodium symporter activity, TAS1 genes
mannose binding, IEA1 genes
mannose binding, ISS1 genes
mannose binding, NR1 genes
membrane attack complex, NR1 genes
membrane attack complex, TAS1 genes
mitochondrial outer membrane, ISS1 genes
mitochondrial outer membrane translocase complex, NAS1 genes
mitochondrial outer membrane translocase complex, TAS1 genes
mitochondrial inner membrane, IDA1 genes
mitochondrial inner membrane, IEP1 genes
mitochondrial electron transport chain, IDA1 genes
mitochondrial electron transport chain, NR1 genes
mitochondrial intermembrane space, IEA1 genes
mitochondrial intermembrane space, ISS1 genes
mitochondrial matrix, IEP1 genes
mitochondrial ribosome, IDA1 genes
mitochondrial ribosome, IEA1 genes
mitochondrial ribosome, ISS1 genes
mitochondrial ribosome, TAS1 genes
mitochondrial large ribosomal subunit, NR1 genes
mitochondrial small ribosomal subunit, TAS1 genes
microsome, IDA1 genes
microtubule organizing center, TAS1 genes
mRNA cleavage and polyadenylation specificity factor complex, IDA1 genes
mRNA cleavage factor complex, NAS1 genes
microtubule, ISS1 genes
microtubule associated complex, IDA1 genes
microtubule associated complex, ISS1 genes
microtubule associated complex, NR1 genes
microvillus, TAS1 genes
monosaccharide metabolism, NAS1 genes
mannose metabolism, NR1 genes
myo-inositol biosynthesis, IEA1 genes
main pathways of carbohydrate metabolism, IEA1 genes
malate metabolism, NR1 genes
mitochondrial electron transport, NADH to ubiquinone, NAS1 genes
mitochondrial electron transport, ubiquinol to cytochrome c, NAS1 genes
mismatch repair, IDA1 genes
mismatch repair, ISS1 genes
mRNA capping, IEA1 genes
mRNA splice site selection, ISS1 genes
mRNA polyadenylation, IDA1 genes
mRNA polyadenylation, NAS1 genes
mRNA cleavage, IDA1 genes
mRNA editing, ISS1 genes
mRNA processing, ISS1 genes
mRNA catabolism, IMP1 genes
mRNA catabolism, NAS1 genes
mRNA-nucleus export, IPI1 genes
mRNA-nucleus export, NR1 genes
membrane protein ectodomain proteolysis, TAS1 genes
methionine metabolism, IEA1 genes
mitochondrial processing, TAS1 genes
Mo-molybdopterin cofactor biosynthesis, NAS1 genes
Mo-molybdopterin cofactor biosynthesis, TAS1 genes
mitochondrial transport, NAS1 genes
mitochondrial citrate transport, TAS1 genes
metal ion homeostasis, NAS1 genes
muscle contraction, IEA1 genes
membrane fusion, NAS1 genes
membrane fusion, NR1 genes
mitochondrial membrane organization and biogenesis, TAS1 genes
microtubule-based movement, ISS1 genes
microtubule nucleation, TAS1 genes
microtubule stabilization, IMP1 genes
microtubule stabilization, ISS1 genes
microtubule stabilization, NR1 genes
mitotic spindle assembly, IDA1 genes
mitotic spindle assembly, IEP1 genes
mitotic spindle assembly, NAS1 genes
mitotic sister chromatid cohesion, TAS1 genes
mitosis, IDA1 genes
mitotic chromosome condensation, IDA1 genes
mitotic chromosome condensation, NAS1 genes
mitotic chromosome condensation, TAS1 genes
mitotic chromosome movement, TAS1 genes
mitotic metaphase plate congression, IDA1 genes
mitotic metaphase plate congression, TAS1 genes
mitotic metaphase/anaphase transition, TAS1 genes
mitotic spindle checkpoint, NR1 genes
mitotic G2 checkpoint, TAS1 genes
meiosis, IDA1 genes
meiosis, ISS1 genes
meiosis, NAS1 genes
meiotic recombination, IEA1 genes
meiotic recombination, ISS1 genes
meiotic recombination, NAS1 genes
meiotic prophase II, TAS1 genes
male meiosis, ISS1 genes
male meiosis, TAS1 genes
male meiosis I, TAS1 genes
muscarinic acetylcholine receptor, adenylate cyclase inhibiting pathway, NR1 genes
muscarinic acetylcholine receptor, adenylate cyclase inhibiting pathway, TAS1 genes
metabotropic glutamate receptor, phospholipase C activating pathway, TAS1 genes
metabotropic glutamate receptor signaling pathway, TAS1 genes
mesoderm development, ISS1 genes
mesoderm development, NR1 genes
mesoderm cell fate specification, TAS1 genes
mesoderm migration, IMP1 genes
myogenesis, ISS1 genes
myogenesis, NAS1 genes
memory, TAS1 genes
mating behavior, TAS1 genes
mating, TAS1 genes
mechanosensory behavior, TAS1 genes
motor axon guidance, TAS1 genes
mitochondrial fusion, TAS1 genes
metabolism, IC1 genes
metabolism, NR1 genes
methyltransferase activity, IDA1 genes
methyltransferase activity, TAS1 genes
metalloendopeptidase inhibitor activity, IDA1 genes
metalloendopeptidase inhibitor activity, IEA1 genes
metalloexopeptidase activity, TAS1 genes
manganese superoxide dismutase activity, IDA1 genes
manganese superoxide dismutase activity, ISS1 genes
metallocarboxypeptidase D activity, TAS1 genes
melatonin receptor activity, IEA1 genes
methionine synthase activity, IEA1 genes
methionine catabolism, NR1 genes
magnesium ion transporter activity, TAS1 genes
mercury ion transporter activity, IEA1 genes
mevalonate transporter activity, TAS1 genes
multidrug transporter activity, NR1 genes
methotrexate transporter activity, TAS1 genes
microtubule cytoskeleton, IDA1 genes
microtubule cytoskeleton, IEP1 genes
mercury ion transport, IEA1 genes
mevalonate transport, TAS1 genes
monoamine transport, IDA1 genes
mannosidase activity, TAS1 genes
molecular hydrogen transport, NAS1 genes
membrane, IC1 genes
maleylacetoacetate isomerase activity, TAS1 genes
membrane organization and biogenesis, NAS1 genes
maintenance of rhodopsin mediated signaling, TAS1 genes
mRNA metabolism, ISS1 genes
mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity, NAS1 genes
malate dehydrogenase activity, IEA1 genes
malate dehydrogenase (oxaloacetate-decarboxylating) activity, IEA1 genes
monodehydroascorbate reductase (NADH) activity, NAS1 genes
myosin binding, IEA1 genes
myosin binding, ISS1 genes
myosin binding, NAS1 genes
molybdopterin synthase complex, NAS1 genes
mannose biosynthesis, IEA1 genes
myo-inositol catabolism, ISS1 genes
myofibril, TAS1 genes
microvillus biogenesis, NAS1 genes
microspike biogenesis, NAS1 genes
mitochondrial crista, IDA1 genes
myeloid blood cell differentiation, IDA1 genes
myeloid blood cell differentiation, TAS1 genes
MHC class I receptor activity, NR1 genes
manganese ion binding, ISS1 genes
melatonin biosynthesis, IEA1 genes
melatonin biosynthesis, TAS1 genes
megakaryocyte differentiation, NAS1 genes
monocyte differentiation, IDA1 genes
macrophage differentiation, NAS1 genes
macrophage differentiation, TAS1 genes
male sex determination, NAS1 genes
melanin-concentrating hormone receptor activity, IEA1 genes
melanocyte differentiation, NAS1 genes
muscle fiber, NAS1 genes
methylarsonite methyltransferase activity, ISS1 genes
Mre11 complex, IEA1 genes
mammary gland development, IDA1 genes
mitotic spindle positioning and orientation, NAS1 genes
macrophage activation, IMP1 genes
macrophage activation, ISS1 genes
monocyte activation, TAS1 genes
MHC protein binding, NAS1 genes
MHC class I protein binding, TAS1 genes
MHC class II protein binding, NAS1 genes
melanosome, IDA1 genes
myelination, NAS1 genes
muscle cell differentiation, IDA1 genes
muscle cell differentiation, NAS1 genes
MHC class I peptide loading complex, NAS1 genes
myosin II binding, NAS1 genes
maintenance of epithelial cell polarity, ISS1 genes
maintenance of epithelial cell polarity, TAS1 genes
MAPK nucleus export, TAS1 genes
myoblast differentiation, IDA1 genes
myoblast differentiation, ISS1 genes
myoblast differentiation, NAS1 genes
macrophage chemotaxis, NAS1 genes
macrophage chemotaxis, TAS1 genes
methionine adenosyltransferase complex, IDA1 genes
methionine adenosyltransferase regulator activity, IDA1 genes
methionine adenosyltransferase regulator activity, ISS1 genes
mitogen-activated protein kinase p38 binding, IGI1 genes
malonyl-CoA decarboxylase activity, IEA1 genes
AS3D: Alternative Splicing Structural Genomics Projects
CARB/UMBI