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BRD7P2 bromodomain containing 7 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 647076, updated on 13-May-2022

Summary

Official Symbol
BRD7P2provided by HGNC
Official Full Name
bromodomain containing 7 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:33541
See related
Ensembl:ENSG00000184100 AllianceGenome:HGNC:33541
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 BRD7P2 in Genome Data Viewer
Location:
3q25.33
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (160100691..160102912)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (162875287..162877508)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (159818478..159820699)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene IL12A antisense RNA 1 Neighboring gene uncharacterized LOC124906252 Neighboring gene long intergenic non-protein coding RNA 1100 Neighboring gene Sharpr-MPRA regulatory region 6612 Neighboring gene Sharpr-MPRA regulatory region 14309

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_009641.3 

    Range
    101..2322
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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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    160100691..160102912
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    162875287..162877508
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)