TRPM1
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Homo sapiens |
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TRPM1 is differentially expressed in 120 experiments: 64 organism parts: blood, skeletal muscle, ... (62 more);, 94 disease states: normal, melanoma, ... (92 more);, 34 cell types 85 cell lines 8 compound treatments and 55 other conditions. |
| Synonyms |
MLSN1, LTRPC1 |
| Orthologs |
Trpm1
(Mus musculus)
TRPM1
(Gallus gallus)
Trpm1
(Rattus norvegicus)
TRPM1
(Bos taurus)
trpm1
(Danio rerio)
trpm1b
(Danio rerio)
trpm1
(Xenopus laevis)
TRPM1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
plasma membrane, transport, calcium channel activity, ion transport, visual perception, membrane, ion channel activity, response to stimulus, integral to plasma membrane, receptor activity, integral to membrane, transmembrane transport, cellular response to light stimulus, calcium ion transmembrane transport |
| Gene Ontology ID |
GO:0016020, GO:0016021, GO:0007601, GO:0004872, GO:0005886, GO:0005887, GO:0055085, GO:0006811, GO:0006810, GO:0005216, GO:0005262, GO:0050896, GO:0071482, GO:0070588 |
| Ensembl Family Description |
TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL SUBFAMILY M MEMBER LONG TRANSIENT RECEPTOR POTENTIAL CHANNEL |
| InterPro ID |
IPR005821 |
| Ensembl Family |
ENSFM00250000000305 |
| InterPro Term |
Ion_trans |
| Description |
transient receptor potential cation channel, subfamily M, member 1 [Source:HGNC Symbol;Acc:7146] |
| Ensembl Protein ID |
ENSP00000380895, ENSP00000380897, ENSP00000256552, ENSP00000437849, ENSP00000452946, ENSP00000454077, ENSP00000453644, ENSP00000453851, ENSP00000453119, ENSP00000453477 |
| UniGene ID |
Hs.155942 |
| HGNC Symbol |
TRPM1 |
| Entrez Gene ID |
4308 |
| EMBL-Bank ID |
AB115501, AB115502, AB115500, AC090829, AB115498, AB115499, AF071787, CH471216, AC009562, HM135791 |
| Ensembl Gene ID |
ENSG00000134160 |
| RefSeq ID |
NP_002411, NM_002420 |
| UniProt Accession |
Q7Z4N2, D9IDV3, F8W865 |
| Ensembl Transcript ID |
ENST00000542188, ENST00000397795, ENST00000397793, ENST00000256552, ENST00000559179, ENST00000559177, ENST00000560801, ENST00000560658, ENST00000558768, ENST00000558445, ENST00000557948, ENST00000558212, ENST00000558070 |
| Gene-Disease Assocation |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C |
| Design Element |
41564_at, Hs.166845.0.A1_3p_at, ENST00000558212, 206479_at, 237070_at, ENST00000559177, ENST00000560658, g6006023_3p_at, ENST00000560801, ENST00000256552, ENST00000558768, 49609_r_at, ENST00000559179, ENST00000557948, ENST00000558445, ENST00000397795, Hs.166845.0.A1_3p_s_at, ENST00000558070, ENST00000397793, 237069_s_at, 62717_at, ENST00000542188 |
| Search EB-eye |
ENSG00000134160
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