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BNIP3P42 BCL2 interacting protein 3 pseudogene 42 [ Homo sapiens (human) ]

Gene ID: 106481697, updated on 17-Sep-2024

Summary

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Official Symbol
BNIP3P42provided by HGNC
Official Full Name
BCL2 interacting protein 3 pseudogene 42provided by HGNC
Primary source
HGNC:HGNC:49722
See related
Ensembl:ENSG00000223974 AllianceGenome:HGNC:49722
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 BNIP3P42 in Genome Data Viewer
Location:
7q11.21
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (64551498..64552066)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (65758992..65759560)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (64011876..64012444)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene vomeronasal 1 receptor 41 pseudogene Neighboring gene heterogeneous nuclear ribonucleoprotein C pseudogene 7 Neighboring gene zinc finger protein 680 Neighboring gene MPRA-validated peak6531 silencer Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:64014505-64015010 Neighboring gene Sharpr-MPRA regulatory region 12132 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26058 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18196 Neighboring gene PAGE family member 4 pseudogene Neighboring gene IgLON family member 5 pseudogene Neighboring gene uncharacterized LOC124901657

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

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Other Names

  • BCL2/adenovirus E1B 19kDa interacting protein 3 pseudogene 42

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_045027.1 

    Range
    101..669
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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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    64551498..64552066
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    65758992..65759560
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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