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BCRP5 BCR pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 648980, updated on 13-May-2022

Summary

Official Symbol
BCRP5provided by HGNC
Official Full Name
BCR pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:1018
See related
AllianceGenome:HGNC:1018
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
BCRL5
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Genomic context

See BCRP5 in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (20695438..20698959, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (21104147..21107668, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (21049726..21053247, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene ABHD17A pseudogene 4 Neighboring gene uncharacterized LOC107985584 Neighboring gene POM121 transmembrane nucleoporin like 4, pseudogene Neighboring gene transmembrane protein 191A (pseudogene) Neighboring gene phosphatidylinositol 4-kinase alpha Neighboring gene Sharpr-MPRA regulatory region 10582 Neighboring gene serpin family D member 1

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_009418.2 

    Range
    101..3622
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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
    20695438..20698959 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    21104147..21107668 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)