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Protein Coding Gene : Trpm1 transient receptor potential cation channel, subfamily M, member 1
Primary Identifier  MGI:1330305 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  17364
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables monoatomic cation channel activity. Involved in cellular response to light stimulus. Acts upstream of or within protein localization; retinal rod cell development; and signal transduction. Located in new growing cell tip. Is active in cell tip and dendrite. Is expressed in foregut; reproductive system; and sensory organ. Human ortholog(s) of this gene implicated in congenital stationary night blindness and congenital stationary night blindness 1C. Orthologous to human TRPM1 (transient receptor potential cation channel subfamily M member 1).
PHENOTYPE: Homozygous mutants have defects in rod and cone electrophysiology affecting the photoresponses. [provided by MGI curators]
  • synonyms:
  • melastatin 1,
  • AI606771,
  • retinal degeneration 15,
  • MGI:4867500,
  • MGI:3036274,
  • Trpm1,
  • expressed sequence AI606771,
  • transient receptor potential cation channel, subfamily M, member 1,
  • melastatin,
  • RIKEN cDNA 4732499L03 gene,
  • rd15,
  • LTRPC1,
  • Mlsn1,
  • 4732499L03Rik,
  • MGI:2142011
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6 Involved In Mutations

Trail: ProteinCodingGene

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

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Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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