SLC25A43 solute carrier family 25 member 43
Gene ID: 203427, updated on 17-Sep-2024Gene type: protein coding
- See all available tests in GTR for this gene
- Go to complete Gene record for SLC25A43
- Go to Variation Viewer for SLC25A43 variants
Summary
This gene encodes a member of the mitochondrial carrier family of proteins.[provided by RefSeq, Dec 2009]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. GeneReviews: Not available |
Genomic context
- Location:
- Xq24
- Sequence:
- Chromosome: X; NC_000023.11 (119399336..119454478)
- Total number of exons:
- 9
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SLC25A43 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
- SLC25A43 @ LOVD
- Variation ViewerRelated Variants
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