CALHM1 calcium homeostasis modulator 1
Gene ID: 255022, updated on 2-Nov-2024Gene type: protein coding
Also known as: FAM26C
- See all available tests in GTR for this gene
- Go to complete Gene record for CALHM1
- Go to Variation Viewer for CALHM1 variants
Summary
This gene encodes a calcium channel that plays a role in processing of amyloid-beta precursor protein. A polymorphism at this locus has been reported to be associated with susceptibility to late-onset Alzheimer's disease in some populations, but the pathogenicity of this polymorphism is unclear.[provided by RefSeq, Mar 2010]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide association analysis identifies 13 new risk loci for schizophrenia. GeneReviews: Not available |
Genomic context
- Location:
- 10q24.33
- Sequence:
- Chromosome: 10; NC_000010.11 (103453240..103458900, complement)
- Total number of exons:
- 2
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CALHM1 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- CALHM1 @ LOVD
- CALHM1 homepage - Australian Human Variome Project
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- 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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