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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
transient receptor potential cation channel subfamily M member 3
Summary
- Gene Symbol
-
- TRPM3
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calcium channel
- Cataract
- Cell membrane
- Coiled coil
- Disease variant
- Epilepsy
- Intellectual disability
- Ion channel
- Proteomics identification
- Receptor
- Reference proteome
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| monoatomic cation transmembrane transport | ||
| metal ion transport | ||
| monoatomic cation transport | ||
| calcium ion transmembrane transport | ||
| protein tetramerization |
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| calcium channel activity | ||
| monoatomic cation channel activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Transient receptor potential cation channel subfamily M member
- Functional Category
-
- E: Amino acid transport and metabolism
- J: Translation, ribosomal structure and biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| ATP binding |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060246 | MASA syndrome | |
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | |
| DOID:10629 | microphthalmia | |
| DOID:83 | cataract |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 36694 | FB:FBgn0265194 | |||
| 172646 | WB:WBGene00001651 | |||
| 178031 | WB:WBGene00001795 | |||
| 178036 | WB:WBGene00001796 | |||
| 226025 | MGI:2443101 | MOUSE26744 | ||
| 309407 | RGD:1304888 | RATNO20827 | ||
| 464521 | 9598_0:00281d | PANTR44090 | ||
| 476326 | CANLF00435 | |||
| 565807 | ZFIN:ZDB-GENE-060531-95 | DANRE36644 | ||
| 702898 | MACMU13140 |
