SLF1 SMC5-SMC6 complex localization factor 1
Gene ID: 84250, updated on 10-Oct-2024Gene type: protein coding
Also known as: BRCTx; BRCTD1; ANKRD32
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- Go to complete Gene record for SLF1
- Go to Variation Viewer for SLF1 variants
Summary
Enables ubiquitin protein ligase binding activity. Involved in several processes, including positive regulation of cellular component organization; positive regulation of double-strand break repair; and protein localization to site of double-strand break. Located in nucleoplasm and site of double-strand break. [provided by Alliance of Genome Resources, Apr 2022]
Genomic context
- Location:
- 5q15
- Sequence:
- Chromosome: 5; NC_000005.10 (94618231..94697621)
- Total number of exons:
- 23
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SLF1 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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