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BNIP3P32 BCL2 interacting protein 3 pseudogene 32 [ Homo sapiens (human) ]

Gene ID: 106480283, updated on 10-Dec-2024

Summary

Official Symbol
BNIP3P32provided by HGNC
Official Full Name
BCL2 interacting protein 3 pseudogene 32provided by HGNC
Primary source
HGNC:HGNC:49712
See related
Ensembl:ENSG00000268830 AllianceGenome:HGNC:49712
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 BNIP3P32 in Genome Data Viewer
Location:
19p12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (22447934..22448777, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (22586549..22587392, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (22630736..22631579, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ribosomal protein L34 pseudogene 34 Neighboring gene zinc finger protein 98 Neighboring gene uncharacterized LOC105376917 Neighboring gene BCL2 interacting protein 3 pseudogene 33 Neighboring gene zinc finger protein 209, pseudogene

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_044130.1 

    Range
    101..944
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    22447934..22448777 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    22586549..22587392 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)