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NPM1P22 nucleophosmin 1 pseudogene 22 [ Homo sapiens (human) ]

Gene ID: 390411, updated on 17-Sep-2024

Summary

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Official Symbol
NPM1P22provided by HGNC
Official Full Name
nucleophosmin 1 pseudogene 22provided by HGNC
Primary source
HGNC:HGNC:39679
See related
AllianceGenome:HGNC:39679
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 NPM1P22 in Genome Data Viewer
Location:
13q21.32
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (67831564..67832762, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (67052482..67053680, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (68405696..68406894, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984622 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:68310642-68311540 Neighboring gene Sharpr-MPRA regulatory region 9294 Neighboring gene uncharacterized LOC124903238 Neighboring gene uncharacterized LOC105370251 Neighboring gene BCR pseudogene 9 Neighboring gene VISTA enhancer hs575 Neighboring gene olfactory receptor family 7 subfamily E member 111 pseudogene Neighboring gene olfactory receptor family 7 subfamily E member 33 pseudogene

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 Variation Viewer (GRCh37.p13)

General gene information

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Other Names

  • nucleophosmin (nucleolar phosphoprotein B23, numatrin) pseudogene
  • nucleophosmin 1 (nucleolar phosphoprotein B23, numatrin) pseudogene 22
  • nucleophosmin 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_011393.4 

    Range
    101..1299
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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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    67831564..67832762 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    67052482..67053680 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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