SLC30A9 solute carrier family 30 member 9
Gene ID: 10463, updated on 19-Sep-2024Gene type: protein coding
Also known as: HUEL; ZNT9; GAC63; C4orf1; BILAPES
- See all available tests in GTR for this gene
- Go to complete Gene record for SLC30A9
- Go to Variation Viewer for SLC30A9 variants
Summary
Predicted to enable nuclear receptor coactivator activity. Involved in cellular zinc ion homeostasis and zinc ion transport. Located in several cellular components, including cytoplasmic vesicle; cytoskeleton; and endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome | not available |
Genomic context
- Location:
- 4p13
- Sequence:
- Chromosome: 4; NC_000004.12 (41990530..42090461)
- Total number of exons:
- 18
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for SLC30A9 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
- Variation ViewerRelated Variants
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