SLC47A1 solute carrier family 47 member 1
Gene ID: 55244, updated on 5-Mar-2024Gene type: protein coding
Also known as: MATE1
- See all available tests in GTR for this gene
- Go to complete Gene record for SLC47A1
- Go to Variation Viewer for SLC47A1 variants
Summary
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]
Genomic context
- Location:
- 17p11.2
- Sequence:
- Chromosome: 17; NC_000017.11 (19533854..19579034)
- Total number of exons:
- 17
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SLC47A1 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
- Variation ViewerRelated Variants
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