Gene
trpm1b
- ID
- ZDB-GENE-070424-31
- Name
- transient receptor potential cation channel, subfamily M, member 1b
- Symbol
- trpm1b Nomenclature History
- Previous Names
-
- trpm1a (1)
- zgc:162329
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Predicted to have ion channel activity. Predicted to be involved in ion transport; protein tetramerization; and transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in congenital stationary night blindness and congenital stationary night blindness 1C. Is expressed in melanoblast; neural crest cell; and retina. Orthologous to human TRPM1 (transient receptor potential cation channel subfamily M member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital stationary night blindness 1C | Alliance | Night blindness, congenital stationary (complete), 1C, autosomal recessive | 613216 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Transient receptor potential cation channel M | TRPM, SLOG domain |
|---|---|---|---|
|
UniProtKB:A0A8M9PV08
|
410 | ||
|
UniProtKB:A0A8M9P6H0
|
343 | ||
|
UniProtKB:A3KNP8
|
297 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available