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BNIP3P2 BCL2 interacting protein 3 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100421754, updated on 13-May-2022

Summary

Official Symbol
BNIP3P2provided by HGNC
Official Full Name
BCL2 interacting protein 3 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39655
See related
Ensembl:ENSG00000236097 AllianceGenome:HGNC:39655
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 BNIP3P2 in Genome Data Viewer
Location:
22q11.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (15349488..15350019)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (15924647..15925178)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (16627944..16628475, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene putative ankyrin repeat domain-containing protein 30B-like Neighboring gene U6 spliceosomal RNA Neighboring gene zinc finger protein 43 pseudogene Neighboring gene YME1L1 pseudogene 1 Neighboring gene olfactory receptor family 11 subfamily H 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_027406.1 

    Range
    101..632
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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
    15349488..15350019
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    15924647..15925178
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)