AP5S1 adaptor related protein complex 5 subunit sigma 1
Gene ID: 55317, updated on 2-Nov-2024Gene type: protein coding
Also known as: C20orf29
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- Go to complete Gene record for AP5S1
- Go to Variation Viewer for AP5S1 variants
Summary
Involved in double-strand break repair via homologous recombination and endosomal transport. Located in several cellular components, including late endosome; lysosome; and nucleoplasm. Part of AP-type membrane coat adaptor complex. [provided by Alliance of Genome Resources, Nov 2024]
Genomic context
- Location:
- 20p13
- Sequence:
- Chromosome: 20; NC_000020.11 (3820547..3828838)
- Total number of exons:
- 3
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for AP5S1 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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