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BNIP3P43 BNIP3 pseudogene 43 [ Homo sapiens (human) ]

Gene ID: 127379721, updated on 10-Oct-2023

Summary

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Official Symbol
BNIP3P43provided by HGNC
Official Full Name
BNIP3 pseudogene 43provided by HGNC
Primary source
HGNC:HGNC:56379
See related
Ensembl:ENSG00000237202
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

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See BNIP3P43 in Genome Data Viewer
Location:
21q11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (13120244..13120807)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (11464596..11465159)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 30B pseudogene 2 Neighboring gene vomeronasal 1 receptor 109 pseudogene Neighboring gene zinc finger protein 355, pseudogene Neighboring gene fibroblast growth factor 7 pseudogene 2 Neighboring gene ankyrin repeat domain 30B pseudogene 1 Neighboring gene microRNA 3156-3

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General gene information

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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_115712.1 

    Range
    101..664
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    13120244..13120807
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    11464596..11465159
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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