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    BRIP1 BRCA1 interacting DNA helicase 1 [ Homo sapiens (human) ]

    Gene ID: 83990, updated on 10-Dec-2024

    Summary

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    Official Symbol
    BRIP1provided by HGNC
    Official Full Name
    BRCA1 interacting DNA helicase 1provided by HGNC
    Primary source
    HGNC:HGNC:20473
    See related
    Ensembl:ENSG00000136492 MIM:605882; AllianceGenome:HGNC:20473
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    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]
    Annotation information
    Note: BACH1 (Gene ID: 571) and BRIP1 (Gene ID: 83990) share the BACH1 symbol/alias in common. BACH1 is a widely used alternative name for BRCA1 interacting protein C-terminal helicase 1 (BRIP1), which can be confused with the official symbol for BTB domain and CNC homolog 1 (BACH1). [10 Jul 2018]
    Expression
    Broad expression in testis (RPKM 1.9), bone marrow (RPKM 1.0) and 16 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See BRIP1 in Genome Data Viewer
    Location:
    17q23.2
    Exon count:
    23
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (61679139..61863528, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (62547944..62734245, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (59756500..59940889, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904042 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:59531395-59532276 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:59532277-59533157 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59539816-59540478 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59541142-59541803 Neighboring gene Sharpr-MPRA regulatory region 11492 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59553878-59554580 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59554581-59555281 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59563448-59564310 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59564311-59565173 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:59591549-59592049 Neighboring gene T-box transcription factor 4 Neighboring gene Sharpr-MPRA regulatory region 7395 Neighboring gene nascent polypeptide associated complex subunit alpha 2 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr17:59835525-59836270 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 12535 Neighboring gene VISTA enhancer hs778 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 12536 Neighboring gene integrator complex subunit 2 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8802 Neighboring gene mediator complex subunit 13 Neighboring gene RNA, 7SL, cytoplasmic 800, pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

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    Related articles in PubMed

    1. Association between BRIP1 (BACH1) polymorphisms and breast cancer risk: a meta-analysis. Pabalan N, et al. Breast Cancer Res Treat, 2013 Jan. PMID 23225146
    2. Cancer-associated mutations in the iron-sulfur domain of FANCJ affect G-quadruplex metabolism. Odermatt DC, et al. PLoS Genet, 2020 Jun. PMID 32542039, Free PMC Article
    3. Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families. Ray AM, et al. Br J Cancer, 2009 Dec 15. PMID 19935797, Free PMC Article
    4. FANCJ helicase promotes DNA end resection by facilitating CtIP recruitment to DNA double-strand breaks. Nath S, et al. PLoS Genet, 2020 Apr. PMID 32251466, Free PMC Article
    5. Landscape of BRIP1 molecular lesions in gastrointestinal cancers from published genomic studies. Voutsadakis IA. World J Gastroenterol, 2020 Mar 21. PMID 32231423, Free PMC Article

    See all (214) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. FANCJ promotes PARP1 activity during DNA replication that is essential in BRCA1 deficient cells.
      Title: FANCJ promotes PARP1 activity during DNA replication that is essential in BRCA1 deficient cells.
    2. Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.
      Title: Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.
    3. Association of BARD1 and BRIP1 Gene Polymorphisms with the Risk of Uveal Melanoma.
      Title: Association of BARD1 and BRIP1 Gene Polymorphisms with the Risk of Uveal Melanoma.
    4. UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C, RAD51D, BRIP1 and PALB2.
      Title: UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C, RAD51D, BRIP1 and PALB2.
    5. Spectrum of BRCA1 interacting helicase 1 aberrations and potential prognostic and therapeutic implication: a pan cancer analysis.
      Title: Spectrum of BRCA1 interacting helicase 1 aberrations and potential prognostic and therapeutic implication: a pan cancer analysis.
    6. Multimolecular characteristics and role of BRCA1 interacting protein C-terminal helicase 1 (BRIP1) in human tumors: a pan-cancer analysis.
      Title: Multimolecular characteristics and role of BRCA1 interacting protein C-terminal helicase 1 (BRIP1) in human tumors: a pan-cancer analysis.
    7. Dominant-negative pathogenic variant BRIP1 c.1045G>C is a high-risk allele for non-mucinous epithelial ovarian cancer: A case-control study.
      Title: Dominant-negative pathogenic variant BRIP1 c.1045G>C is a high-risk allele for non-mucinous epithelial ovarian cancer: A case-control study.
    8. BRIP1 rs10744996C>A variant increases the risk of chronic obstructive pulmonary disease in the Mongolian population of northern China.
      Title: BRIP1 rs10744996C>A variant increases the risk of chronic obstructive pulmonary disease in the Mongolian population of northern China.
    9. A Novel Role for BRIP1/FANCJ in Neuronal Cells Health and in Resolving Oxidative Stress-Induced DNA Lesions.
      Title: A Novel Role for BRIP1/FANCJ in Neuronal Cells Health and in Resolving Oxidative Stress-Induced DNA Lesions.
    10. BRIP1, a Gene Potentially Implicated in Familial Colorectal Cancer Type X.
      Title: BRIP1, a Gene Potentially Implicated in Familial Colorectal Cancer Type X.
    Submit: New GeneRIF Correction See all GeneRIFs (116)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Familial cancer of breast
    MedGen: C0346153 OMIM: 114480 GeneReviews: BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer
    		not available
    Fanconi anemia complementation group J
    MedGen: C1836860 OMIM: 609054 GeneReviews: Fanconi Anemia
    		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

    EBI GWAS Catalog

    Description
    Gene network analysis in a pediatric cohort identifies novel lung function genes.
    EBI GWAS Catalog
    Mutations in BRIP1 confer high risk of ovarian cancer.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • FLJ90232, MGC126521, MGC126523

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables 4 iron, 4 sulfur cluster binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables 5'-3' DNA helicase activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables ATP hydrolysis activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables ATP-dependent H2AZ histone chaperone activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables ATP-dependent H3-H4 histone complex chaperone activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables DNA binding NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    enables DNA clamp loader activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables DNA helicase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables DNA helicase activity NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    enables RNA helicase activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables chromatin binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables chromatin extrusion motor activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables cohesin loader activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables isomerase activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables metal ion binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in DNA damage checkpoint signaling NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in DNA duplex unwinding IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in DNA repair NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in G-quadruplex DNA unwinding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in cellular response to angiotensin IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in cellular response to hypoxia IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in cellular response to vitamin IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in chiasma assembly IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in chromatin looping IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in chromatin remodeling IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in double-strand break repair NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in double-strand break repair involved in meiotic recombination IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in homologous recombination NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in meiotic DNA double-strand break processing involved in reciprocal meiotic recombination IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in negative regulation of cell population proliferation IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in negative regulation of gene expression IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in nucleotide-excision repair IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in protein-DNA covalent cross-linking repair IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    acts_upstream_of_or_within regulation of transcription by RNA polymerase II IDA
    Inferred from Direct Assay
    more info
    		  
    involved_in response to toxic substance IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in seminiferous tubule development IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in spermatid development IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in spermatogonial cell division IEA
    Inferred from Electronic Annotation
    more info
    		  
    Component Evidence Code Pubs
    part_of BRCA1-B complex IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in nuclear membrane IDA
    Inferred from Direct Assay
    more info
    		  
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
    		  
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in nucleus NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    is_active_in replication fork IDA
    Inferred from Direct Assay
    more info
    		 PubMed 

    General protein information

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    Preferred Names
    Fanconi anemia group J protein
    Names
    ATP-dependent RNA helicase BRIP1
    BRCA1 interacting helicase 1
    BRCA1 interacting protein C-terminal helicase 1
    BRCA1-associated C-terminal helicase 1
    BRCA1-binding helicase-like protein BACH1
    BRCA1/BRCA2-associated helicase 1
    DNA 5'-3' helicase FANCJ
    FANCJ helicase
    NP_114432.2
    XP_011523634.1
    XP_011523635.1
    XP_011523636.1
    XP_011523637.1
    XP_011523638.1
    XP_011523641.1
    XP_011523642.1
    XP_011523643.1
    XP_047292847.1
    XP_047292848.1
    XP_047292849.1
    XP_047292850.1
    XP_047292851.1
    XP_047292852.1
    XP_047292853.1
    XP_047292855.1
    XP_047292856.1
    XP_047292857.1
    XP_047292858.1
    XP_047292859.1
    XP_047292860.1
    XP_054173470.1
    XP_054173471.1
    XP_054173472.1
    XP_054173473.1
    XP_054173474.1
    XP_054173475.1
    XP_054173476.1
    XP_054173477.1
    XP_054173478.1
    XP_054173479.1
    XP_054173480.1
    XP_054173481.1
    XP_054173482.1
    XP_054173483.1
    XP_054173484.1
    XP_054173485.1
    XP_054173486.1
    XP_054173487.1
    XP_054173488.1
    XP_054173489.1
    XP_054173490.1

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_007409.2 RefSeqGene

      Range
      5001..189374
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_300

    mRNA and Protein(s)

    1. NM_032043.3 → NP_114432.2  Fanconi anemia group J protein

      See identical proteins and their annotated locations for NP_114432.2

      Status: REVIEWED

      Source sequence(s)
      AC002994, AC060798, AF360549
      Consensus CDS
      CCDS11631.1
      UniProtKB/Swiss-Prot
      A0A024QZ45, Q3MJE2, Q8NCI5, Q9BX63
      UniProtKB/TrEMBL
      A0A804HJV4
      Related
      ENSP00000259008.2, ENST00000259008.7
      Conserved Domains (2) summary
      cl26203
      Location:18 → 61
      PolC; DNA polymerase III, alpha subunit (gram-positive type) [Replication, recombination and repair]
      cl26947
      Location:245 → 881
      HBB; Helical and beta-bridge domain

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      61679139..61863528 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047436893.1 → XP_047292849.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4

    2. XM_047436891.1 → XP_047292847.1  Fanconi anemia group J protein isoform X2

      UniProtKB/Swiss-Prot
      A0A024QZ45, Q3MJE2, Q8NCI5, Q9BX63
      UniProtKB/TrEMBL
      A0A804HJV4

    3. XM_011525333.4 → XP_011523635.1  Fanconi anemia group J protein isoform X1

      See identical proteins and their annotated locations for XP_011523635.1

      UniProtKB/TrEMBL
      A0A804HJV4
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 901
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:700 → 886
      Helicase_C_2; Helicase C-terminal domain

    4. XM_011525336.3 → XP_011523638.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 861
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:660 → 846
      Helicase_C_2; Helicase C-terminal domain

    5. XM_011525335.4 → XP_011523637.1  Fanconi anemia group J protein isoform X3

      UniProtKB/TrEMBL
      A0A804HJV4
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 881
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:680 → 866
      Helicase_C_2; Helicase C-terminal domain

    6. XM_011525332.4 → XP_011523634.1  Fanconi anemia group J protein isoform X1

      See identical proteins and their annotated locations for XP_011523634.1

      UniProtKB/TrEMBL
      A0A804HJV4
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 901
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:700 → 886
      Helicase_C_2; Helicase C-terminal domain

    7. XM_047436894.1 → XP_047292850.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4

    8. XM_047436892.1 → XP_047292848.1  Fanconi anemia group J protein isoform X2

      UniProtKB/Swiss-Prot
      A0A024QZ45, Q3MJE2, Q8NCI5, Q9BX63
      UniProtKB/TrEMBL
      A0A804HJV4

    9. XM_011525334.3 → XP_011523636.1  Fanconi anemia group J protein isoform X1

      See identical proteins and their annotated locations for XP_011523636.1

      UniProtKB/TrEMBL
      A0A804HJV4
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 901
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:700 → 886
      Helicase_C_2; Helicase C-terminal domain

    10. XM_047436901.1 → XP_047292857.1  Fanconi anemia group J protein isoform X8

      UniProtKB/TrEMBL
      A0A804HJU1, A0A804HK62
      Related
      ENSP00000507646.1, ENST00000683235.1

    11. XM_047436900.1 → XP_047292856.1  Fanconi anemia group J protein isoform X8

      UniProtKB/TrEMBL
      A0A804HJU1, A0A804HK62

    12. XM_011525340.4 → XP_011523642.1  Fanconi anemia group J protein isoform X6

      UniProtKB/TrEMBL
      A0A804HK62
      Conserved Domains (2) summary
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      pfam13307
      Location:700 → 851
      Helicase_C_2; Helicase C-terminal domain

    13. XM_047436903.1 → XP_047292859.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    14. XM_047436895.1 → XP_047292851.1  Fanconi anemia group J protein isoform X5

      UniProtKB/TrEMBL
      A0A804HK62, A0A804HL36

    15. XM_011525339.4 → XP_011523641.1  Fanconi anemia group J protein isoform X5

      UniProtKB/TrEMBL
      A0A804HK62, A0A804HL36
      Related
      ENSP00000508184.1, ENST00000683381.1
      Conserved Domains (3) summary
      TIGR00604
      Location:245 → 809
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2
      cl21455
      Location:700 → 814
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases

    16. XM_047436904.1 → XP_047292860.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    17. XM_047436897.1 → XP_047292853.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0

    18. XM_047436902.1 → XP_047292858.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    19. XM_047436896.1 → XP_047292852.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0
      Related
      ENSP00000463272.2, ENST00000584322.2

    20. XM_047436899.1 → XP_047292855.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0

    21. XM_011525341.4 → XP_011523643.1  Fanconi anemia group J protein isoform X10

      Conserved Domains (2) summary
      TIGR00604
      Location:245 → 648
      rad3; DNA repair helicase (rad3)
      pfam06733
      Location:248 → 415
      DEAD_2; DEAD_2

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      62547944..62734245 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054317499.1 → XP_054173474.1  Fanconi anemia group J protein isoform X2

      UniProtKB/TrEMBL
      A0A804HJV4

    2. XM_054317497.1 → XP_054173472.1  Fanconi anemia group J protein isoform X1

      UniProtKB/TrEMBL
      A0A804HJV4

    3. XM_054317503.1 → XP_054173478.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4

    4. XM_054317502.1 → XP_054173477.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4

    5. XM_054317498.1 → XP_054173473.1  Fanconi anemia group J protein isoform X2

      UniProtKB/TrEMBL
      A0A804HJV4

    6. XM_054317496.1 → XP_054173471.1  Fanconi anemia group J protein isoform X1

      UniProtKB/TrEMBL
      A0A804HJV4

    7. XM_054317501.1 → XP_054173476.1  Fanconi anemia group J protein isoform X4

      UniProtKB/TrEMBL
      A0A804HJV4

    8. XM_054317500.1 → XP_054173475.1  Fanconi anemia group J protein isoform X3

      UniProtKB/TrEMBL
      A0A804HJV4

    9. XM_054317495.1 → XP_054173470.1  Fanconi anemia group J protein isoform X1

      UniProtKB/TrEMBL
      A0A804HJV4

    10. XM_054317511.1 → XP_054173486.1  Fanconi anemia group J protein isoform X8

      UniProtKB/TrEMBL
      A0A804HJU1, A0A804HK62

    11. XM_054317510.1 → XP_054173485.1  Fanconi anemia group J protein isoform X8

      UniProtKB/TrEMBL
      A0A804HJU1, A0A804HK62

    12. XM_054317506.1 → XP_054173481.1  Fanconi anemia group J protein isoform X6

      UniProtKB/TrEMBL
      A0A804HK62

    13. XM_054317514.1 → XP_054173489.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    14. XM_054317513.1 → XP_054173488.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    15. XM_054317505.1 → XP_054173480.1  Fanconi anemia group J protein isoform X5

      UniProtKB/TrEMBL
      A0A804HK62, A0A804HL36

    16. XM_054317504.1 → XP_054173479.1  Fanconi anemia group J protein isoform X5

      UniProtKB/TrEMBL
      A0A804HK62, A0A804HL36

    17. XM_054317509.1 → XP_054173484.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0

    18. XM_054317508.1 → XP_054173483.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0

    19. XM_054317512.1 → XP_054173487.1  Fanconi anemia group J protein isoform X9

      UniProtKB/TrEMBL
      A0A804HK62

    20. XM_054317507.1 → XP_054173482.1  Fanconi anemia group J protein isoform X7

      UniProtKB/TrEMBL
      A0A804HK62, J3QKX0

    21. XM_054317515.1 → XP_054173490.1  Fanconi anemia group J protein isoform X10

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9BX63.2 GenPept UniProtKB/Swiss-Prot:Q9BX63

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