SLC12A8 solute carrier family 12 member 8
Gene ID: 84561, updated on 17-Sep-2024Gene type: protein coding
Also known as: CCC9
- See all available tests in GTR for this gene
- Go to complete Gene record for SLC12A8
- Go to Variation Viewer for SLC12A8 variants
Summary
This gene is thought to be a candidate for psoriasis susceptibility. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2010]
Genomic context
- Location:
- 3q21.2
- Sequence:
- Chromosome: 3; NC_000003.12 (125082644..125212748, complement)
- Total number of exons:
- 14
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SLC12A8 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- 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
- SLC12A8 database
- Variation ViewerRelated Variants
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