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BCRP8 BCR pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 100133044, updated on 13-May-2022

Summary

Official Symbol
BCRP8provided by HGNC
Official Full Name
BCR pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:39076
See related
Ensembl:ENSG00000236794 AllianceGenome:HGNC:39076
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See BCRP8 in Genome Data Viewer
Location:
22q11.23
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (23179923..23180172, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (23602781..23603030, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (23522110..23522359, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene radial spoke head 14 homolog Neighboring gene Sharpr-MPRA regulatory region 7478 Neighboring gene RAB36-BCR intergenic enhancer-blocking element 22-1 Neighboring gene BCR activator of RhoGEF and GTPase Neighboring gene BCR-ABL minor-breakpoint cluster region Neighboring gene Sharpr-MPRA regulatory region 5876 Neighboring gene RNA, 7SL, cytoplasmic 263, pseudogene

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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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_032057.1 

    Range
    101..350
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    23179923..23180172 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    23602781..23603030 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)