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BCRP6 BCR pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 728468, updated on 13-May-2022

Summary

Official Symbol
BCRP6provided by HGNC
Official Full Name
BCR pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:39074
See related
AllianceGenome:HGNC:39074
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 BCRP6 in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (21288229..21294589, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (18941055..18947413)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene gamma-glutamyltransferase 2, pseudogene Neighboring gene E2F transcription factor 6 pseudogene 3 Neighboring gene POM121 transmembrane nucleoporin like 8, pseudogene Neighboring gene family with sequence similarity 230 member H Neighboring gene protein phosphatase 1 regulatory subunit 26 pseudogene 5

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_009421.2 

    Range
    101..6461
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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
    21288229..21294589 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    18941055..18947413
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)