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BNIP3P30 BCL2 interacting protein 3 pseudogene 30 [ Homo sapiens (human) ]

Gene ID: 106481694, updated on 8-Nov-2023

Summary

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Official Symbol
BNIP3P30provided by HGNC
Official Full Name
BCL2 interacting protein 3 pseudogene 30provided by HGNC
Primary source
HGNC:HGNC:49710
See related
Ensembl:ENSG00000268079 AllianceGenome:HGNC:49710
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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Location:
19p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (22203128..22204003)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (22341772..22342647)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (22385930..22386805)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:22322832-22323332 Neighboring gene metadherin pseudogene 5 Neighboring gene vomeronasal 1 receptor 85 pseudogene Neighboring gene zinc finger protein 676 Neighboring gene ReSE screen-validated silencer GRCh37_chr19:22399096-22399311 Neighboring gene zinc finger protein 729 Neighboring gene BCL2 interacting protein 3 pseudogene 31 Neighboring gene H3K27ac hESC enhancer GRCh37_chr19:22504465-22505169 Neighboring gene uncharacterized LOC105372330

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 30

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_043156.1 

    Range
    101..976
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    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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    22203128..22204003
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    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NW_003315965.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    104879..105754 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    22341772..22342647
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    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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