U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    BLID BH3-like motif containing, cell death inducer [ Homo sapiens (human) ]

    Gene ID: 414899, updated on 28-Oct-2024

    Summary

    Official Symbol
    BLIDprovided by HGNC
    Official Full Name
    BH3-like motif containing, cell death inducerprovided by HGNC
    Primary source
    HGNC:HGNC:33495
    See related
    Ensembl:ENSG00000259571 MIM:608853; AllianceGenome:HGNC:33495
    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
    BRCC2
    Summary
    This gene encodes a BH3-like motif containing protein involved in cell death. The encoded protein may induce apoptosis in a caspase-dependent manner. The protein is localized in both the cytoplasm and the mitochondrion. [provided by RefSeq, Aug 2011]
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See BLID in Genome Data Viewer
    Location:
    11q24.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (122115340..122116215, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (122144347..122145222, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (121986048..121986923, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 256, pseudogene Neighboring gene mir-100-let-7a-2-mir-125b-1 cluster host gene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:121976285-121976785 Neighboring gene microRNA 125b-1 Neighboring gene microRNA let-7a-2 Neighboring gene microRNA 10526

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.
    EBI GWAS Catalog
    Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    BH3-like motif-containing cell death inducer
    Names
    breast cancer cell 2
    breast cancer cell protein 2

    NCBI Reference Sequences (RefSeq)

    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.

    mRNA and Protein(s)

    1. NM_001001786.3NP_001001786.2  BH3-like motif-containing cell death inducer

      See identical proteins and their annotated locations for NP_001001786.2

      Status: REVIEWED

      Source sequence(s)
      AF303179, AP001924, BC130363
      Consensus CDS
      CCDS31693.1
      UniProtKB/Swiss-Prot
      A1L416, Q8IZY5
      Related
      ENSP00000453153.1, ENST00000560104.2

    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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      122115340..122116215 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      122144347..122145222 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)