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BRD7P3 bromodomain containing 7 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 23629, updated on 13-May-2022

Summary

Official Symbol
BRD7P3provided by HGNC
Official Full Name
bromodomain containing 7 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:24171
See related
AllianceGenome:HGNC:24171
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
BP75
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Genomic context

See BRD7P3 in Genome Data Viewer
Location:
6q22.31
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (118501373..118503846)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (119686530..119689001)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (118822536..118825009)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene ATP-dependent RNA helicase DDX24-like Neighboring gene uncharacterized LOC105377971 Neighboring gene centrosomal protein 85 like Neighboring gene VISTA enhancer hs2188 Neighboring gene phospholamban

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.

RNA

  1. NR_002730.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC033937, Z99496

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    118501373..118503846
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    119686530..119689001
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_012107.1: Suppressed sequence

    Description
    NM_012107.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.