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
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With trpm1b Human Ortholog
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
Associated With trpm1b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR041491 TRPM, SLOG domain
Domain Details Per Protein
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations