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NDUFB9P3 NADH:ubiquinone oxidoreductase subunit B9 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 100129370, updated on 10-Oct-2023

Summary

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Official Symbol
NDUFB9P3provided by HGNC
Official Full Name
NADH:ubiquinone oxidoreductase subunit B9 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:52271
See related
Ensembl:ENSG00000253994 AllianceGenome:HGNC:52271
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:
8q23.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (110809373..110809894, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (111937984..111938505, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (111821602..111822123, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein SA pseudogene 48 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:111269769-111270270 Neighboring gene ataxin 3 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr8:111844475-111844976 Neighboring gene Sharpr-MPRA regulatory region 9965 Neighboring gene MT-CO1 pseudogene 47 Neighboring gene MT-ND2 pseudogene 35

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)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa pseudogene

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_022402.1 

    Range
    101..622
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    110809373..110809894 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    111937984..111938505 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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