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BCRP7 BCR pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100133163, updated on 13-May-2022

Summary

Official Symbol
BCRP7provided by HGNC
Official Full Name
BCR pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:39075
See related
Ensembl:ENSG00000215544 AllianceGenome:HGNC:39075
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 BCRP7 in Genome Data Viewer
Location:
22q11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (18852284..18858643, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (18839797..18846156, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene gamma-glutamyltransferase 3 pseudogene Neighboring gene E2F transcription factor 6 pseudogene 1 Neighboring gene POM121 transmembrane nucleoporin like 15, pseudogene Neighboring gene family with sequence similarity 230 member F Neighboring gene DiGeorge syndrome critical region gene 6

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_009420.3 

    Range
    101..6460
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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
    18852284..18858643 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)