COL1A2
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Homo sapiens |
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COL1A2 is differentially expressed in 297 experiments: 198 organism parts: placenta, lung, ... (196 more);, 263 disease states: normal, glioblastoma, ... (261 more);, 111 cell types 351 cell lines 25 compound treatments and 72 other conditions. |
| Synonyms |
OI4 |
| Orthologs |
Col1a2
(Mus musculus)
col1a2
(Danio rerio)
ENSCING00000006961
(Ciona intestinalis)
CO1A2_BOVIN
(Bos taurus)
COL1A2
(Gallus gallus)
Col1a2
(Rattus norvegicus)
col1a2
(Xenopus laevis)
CO1A2_CANFA
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
plasma membrane, protein binding, extracellular space, extracellular matrix structural constituent, transforming growth factor beta receptor signaling pathway, extracellular region, blood coagulation, Rho protein signal transduction, identical protein binding, axon guidance, SMAD binding, protein binding, bridging, extracellular matrix, collagen, collagen type I, leukocyte migration, collagen fibril organization, odontogenesis, blood vessel development, skeletal system development, protein heterotrimerization, regulation of blood pressure, platelet-derived growth factor binding, skin morphogenesis, platelet activation, cellular response to amino acid stimulus |
| Gene Ontology ID |
GO:0007179, GO:0007266, GO:0007411, GO:0007596, GO:0030674, GO:0042802, GO:0005615, GO:0005515, GO:0005576, GO:0005581, GO:0005886, GO:0046332, GO:0031012, GO:0005201, GO:0008217, GO:0042476, GO:0048407, GO:0005584, GO:0001568, GO:0001501, GO:0043589, GO:0030168, GO:0070208, GO:0030199, GO:0050900, GO:0071230 |
| InterPro ID |
IPR008160, IPR000885 |
| InterPro Term |
Collagen, Fib_collagen_C |
| Ensembl Family Description |
COLLAGEN ALPHA I CHAIN PRECURSOR ALPHA TYPE I COLLAGEN |
| Ensembl Family |
ENSFM00250000000184 |
| EMBL-Bank ID |
S96821, AF004877, J00114, BC042586, L47668, M22817, M22816, J03464, S98904, K02568, M28985, M35391, AB004317, S41099, M21671, Z74616, M21353, Y00724, X02488, AC002074, K01078, X55525, AC002528, V00503, BC054498, EF202821 |
| Gene-Disease Assocation |
OSTEOGENESIS IMPERFECTA, TYPE IV, OSTEOPOROSIS, EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT, OSTEOGENESIS IMPERFECTA, TYPE I, EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM, OSTEOGENESIS IMPERFECTA, TYPE III, OSTEOGENESIS IMPERFECTA, TYPE II |
| UniProt Accession |
A2TIK1, P08123, Q75N18, F5H299 |
| HGNC Symbol |
COL1A2 |
| Ensembl Protein ID |
ENSP00000297268, ENSP00000439395 |
| Entrez Gene ID |
1278 |
| Ensembl Gene ID |
ENSG00000164692 |
| Description |
collagen, type I, alpha 2 [Source:HGNC Symbol;Acc:2198] |
| UniGene ID |
Hs.629269, Hs.669724, Hs.489142 |
| RefSeq ID |
NP_000080, NM_000089 |
| Ensembl Transcript ID |
ENST00000469732, ENST00000473573, ENST00000497316, ENST00000467931, ENST00000488298, ENST00000488121, ENST00000478215, ENST00000545487, ENST00000481570, ENST00000492110, ENST00000464916, ENST00000461525, ENST00000297268 |
| Design Element |
ENST00000488121, ENST00000464916, Hs.179573.1.A1_3p_at, 202404_s_at, ENST00000481570, 32306_g_at, 202403_s_at, ENST00000478215, ENST00000467931, ENST00000545487, ENST00000461525, Z74616_s_at, ENST00000297268, 32305_at, 64347_s_at, 61303_at, g4502946_3p_a_at, 63596_f_at, 229218_at, Hs.179573.0.A1_3p_a_at, ENST00000469732, 60071_s_at, 32307_s_at, ENST00000488298, ENST00000497316, ENST00000473573, 75214_f_at, ENST00000492110, 49162_f_at |
| Search EB-eye |
ENSG00000164692
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