MYH9
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Homo sapiens |
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MYH9 is differentially expressed in 274 experiments: 150 organism parts: lung, brain, ... (148 more);, 200 disease states: normal, glioblastoma, ... (198 more);, 89 cell types 373 cell lines 41 compound treatments and 70 other conditions. |
| Synonyms |
NMMHCA, NMHC-II-A, MHA, EPSTS, FTNS, DFNA17 |
| Orthologs |
MYH9
(Gallus gallus)
MYH9
(Bos taurus)
myh9a
(Danio rerio)
MYH9 (1 of 2)
(Danio rerio)
MYO1
(Saccharomyces cerevisiae)
Myh9
(Mus musculus)
Myh9
(Rattus norvegicus)
zip
(Drosophila melanogaster)
myh9
(Xenopus laevis)
MYH9_CANFA
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
angiogenesis, regulation of cell shape, cytosol, plasma membrane, myosin complex, meiotic spindle organization, integrin complex, actin cytoskeleton reorganization, cell morphogenesis involved in differentiation, protein binding, cleavage furrow, myosin II complex, cell-cell adherens junction, cytoplasm, cell-cell adhesion, cellular component movement, actomyosin contractile ring, cell cortex, protein complex, ruffle, myoblast fusion, ATPase activity, actin filament-based movement, membrane protein ectodomain proteolysis, motor activity, cell leading edge, integrin-mediated signaling pathway, cell adhesion, calmodulin binding, ATP binding, axon guidance, actin cytoskeleton, spindle, neuromuscular junction, meiotic metaphase I, cortical cytoskeleton, nucleus, establishment of meiotic spindle localization, cytokinesis, signalosome, nucleotide binding, actin-dependent ATPase activity, protein homodimerization activity, actin filament binding, protein transport, actin binding, microfilament motor activity, uropod organization, leukocyte migration, immunological synapse, in utero embryonic development, stress fiber, ATP catabolic process, ADP binding, blood vessel endothelial cell migration, platelet formation, uropod, protein anchor, monocyte differentiation, establishment of T cell polarity |
| Gene Ontology ID |
GO:0008180, GO:0008360, GO:0008305, GO:0003774, GO:0003779, GO:0015031, GO:0007132, GO:0007155, GO:0016460, GO:0016459, GO:0007229, GO:0016337, GO:0005938, GO:0007411, GO:0005913, GO:0051295, GO:0007520, GO:0016887, GO:0051015, GO:0042803, GO:0005524, GO:0005516, GO:0005515, GO:0006928, GO:0005737, GO:0015629, GO:0005634, GO:0005886, GO:0005829, GO:0005819, GO:0005826, GO:0030863, GO:0030898, GO:0031252, GO:0006509, GO:0000910, GO:0000904, GO:0000166, GO:0000146, GO:0001726, GO:0043234, GO:0000212, GO:0001525, GO:0031532, GO:0031594, GO:0030048, GO:0032154, GO:0001931, GO:0032796, GO:0001768, GO:0001772, GO:0001701, GO:0001725, GO:0006200, GO:0043531, GO:0043534, GO:0043495, GO:0030220, GO:0030224, GO:0050900 |
| InterPro ID |
IPR000048, IPR001609, IPR002928, IPR004009 |
| Ensembl Family |
ENSFM00270000056424 |
| InterPro Term |
Myosin_head_motor_dom, Myosin_N, Myosin_tail, IQ_motif_EF-hand-BS |
| Ensembl Family Description |
MYOSIN MYOSIN HEAVY CHAIN MYOSIN HEAVY CHAIN NON MUSCLE NON MUSCLE MYOSIN HEAVY CHAIN II |
| Gene-Disease Assocation |
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS, EPSTEIN SYNDROME, SEBASTIAN SYNDROME; SBS, MAY-HEGGLIN ANOMALY; MHA, DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17, FECHTNER SYNDROME; FTNS |
| Ensembl Protein ID |
ENSP00000414852, ENSP00000216181, ENSP00000384631, ENSP00000380408, ENSP00000338576 |
| UniGene ID |
Hs.474751, Hs.713174 |
| EMBL-Bank ID |
BC090921, M81105, Z82215, AB191263, M31013, CH471095, AB290175, M69180, AL832639, CR456526, AK131080, L29141, CR383703 |
| UniProt Accession |
P35579, Q9UMJ0, Q6ZNL4, Q60FE2, Q5BKV1, B1AH99 |
| Entrez Gene ID |
4627 |
| Ensembl Gene ID |
ENSG00000100345 |
| RefSeq ID |
NP_002464, NM_002473 |
| Description |
myosin, heavy chain 9, non-muscle [Source:HGNC Symbol;Acc:7579] |
| HGNC Symbol |
MYH9 |
| Ensembl Transcript ID |
ENST00000495928, ENST00000401701, ENST00000216181, ENST00000475726, ENST00000473022, ENST00000459960, ENST00000463027, ENST00000463293, ENST00000477189, ENST00000486218, ENST00000397231, ENST00000337818, ENST00000472210, ENST00000456729 |
| Design Element |
ENST00000463293, ENST00000477189, ENST00000337818, Hs.146550.0.A2_3p_a_at, ENST00000459960, ENST00000475726, 211926_s_at, 39738_at, M31013_at, ENST00000456729, ENST00000397231, ENST00000472210, 72983_at, ENST00000216181, ENST00000486218, ENST00000473022, ENST00000463027, ENST00000401701, ENST00000495928 |
| Search EB-eye |
ENSG00000100345
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