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BRIP1 BRCA1 interacting helicase 1

Gene ID: 83990, updated on 22-Apr-2024
Gene type: protein coding
Also known as: OF; BACH1; FANCJ

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]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Familial cancer of breastSee labs
Fanconi anemia complementation group J
MedGen: C1836860OMIM: 609054GeneReviews: Fanconi Anemia
See labs
Gene network analysis in a pediatric cohort identifies novel lung function genes.
GeneReviews: Not available
Mutations in BRIP1 confer high risk of ovarian cancer.
GeneReviews: Not available

Copy number response

Description
Copy number response
Triplosensitivity

No evidence available (Last evaluated 2019-02-15)

ClinGen Genome Curation Page
Haploinsufficency

Sufficient evidence for dosage pathogenicity (Last evaluated 2019-02-15)

ClinGen Genome Curation PagePubMed

Genomic context

Location:
17q23.2
Sequence:
Chromosome: 17; NC_000017.11 (61679139..61863528, complement)
Total number of exons:
23

Links

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