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NOP56P2 NOP56 ribonucleoprotein pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 402360, updated on 17-Sep-2024

Summary

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Official Symbol
NOP56P2provided by HGNC
Official Full Name
NOP56 ribonucleoprotein pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:49800
See related
Ensembl:ENSG00000226626 AllianceGenome:HGNC:49800
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 NOP56P2 in Genome Data Viewer
Location:
9p21.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (23681871..23682762)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (23687884..23688775)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (23681869..23682760)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369298 Neighboring gene VISTA enhancer hs309 Neighboring gene uncharacterized LOC101929563 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:23571635-23572216 Neighboring gene SUMO2 pseudogene 2 Neighboring gene ELAV like RNA binding protein 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:23747173-23747672 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:23820186-23821072 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:23821073-23821958 Neighboring gene uncharacterized LOC105375992 Neighboring gene NANOG hESC enhancer GRCh37_chr9:23831326-23831828 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19816 Neighboring gene uncharacterized LOC105375993

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

  • NOP56 ribonucleoprotein homolog 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_023280.2 

    Range
    101..992
    Download
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    23681871..23682762
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    23687884..23688775
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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