BRIP1 (NM_032043) - BRCA1 interacting protein C-terminal helicase 1
Fanconi Anemia Group J Protein
Legend
Mutation impacts
Sites
- C-linked
- N-linked
- O-linked
- S-linked
- SARS-CoV-2
Others
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Mutations Visualisation
Protein summary
The protein encoded by this gene is a member of the RecQ DEAH helicase family and interacts with the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double-strand break repair function of breast cancer, type 1 (BRCA1). This gene may be a target of germline cancer-inducing mutations. [provided by RefSeq, Jul 2008]. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.
Publication Note:
This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Evidence data:
Transcript exon combination :: AF360549.1, BC101472.1 [ECO:0000332]
- Strand
- -
- Chromosome
- 17
- Protein
- 1249 residues
- All mutations
- 1527
- PTM sites
- 61
- CDS
- 59,760,656 - 59,938,900
- Transcription
- 59,756,546 - 59,940,920