TRPC3 transient receptor potential cation channel subfamily C member 3
Gene ID: 7222, updated on 28-Oct-2024Gene type: protein coding
Also known as: TRP3; SCA41
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- Go to complete Gene record for TRPC3
- Go to Variation Viewer for TRPC3 variants
Summary
The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Spinocerebellar ataxia type 41 | See labs |
Genomic context
- Location:
- 4q27
- Sequence:
- Chromosome: 4; NC_000004.12 (121874481..121952060, complement)
- Total number of exons:
- 13
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for TRPC3 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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