ZFIN is now using GRCz12tu for Genomic Data
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
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable monoatomic cation transmembrane transporter activity and monoatomic ion channel activity. Predicted to be involved in monoatomic cation transmembrane transport and protein tetramerization. Predicted to be located in membrane. Is expressed in melanoblast; neural crest cell; and retina. Human ortholog(s) of this gene implicated in congenital stationary night blindness; congenital stationary night blindness 1C; and familial hyperlipidemia. Orthologous to human TRPM1 (transient receptor potential cation channel subfamily M member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 3 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
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
trpm1b-201
(1)
|
Ensembl | 1,678 nt | ||
| mRNA |
trpm1b-202
(1)
|
Ensembl | 4,785 nt |
Interactions and Pathways
No data available
Plasmids
No data available
- Genome Browsers