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HNRNPA1P8 heterogeneous nuclear ribonucleoprotein A1 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 402562, updated on 17-Sep-2024

Summary

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Official Symbol
HNRNPA1P8provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A1 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:39126
See related
AllianceGenome:HGNC:39126
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 HNRNPA1P8 in Genome Data Viewer
Location:
7q21.11
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (84983495..84984839)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (86233326..86234670)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (84612811..84614155)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 3017 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr7:84217793-84218992 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:84266239-84267014 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:84267015-84267788 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_100503 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_100510 Neighboring gene ReSE screen-validated silencer GRCh37_chr7:84344191-84344373 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_100536 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_100640 Neighboring gene VISTA enhancer hs2328 Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 11 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr7:84628763-84629962 Neighboring gene Sharpr-MPRA regulatory region 13705 Neighboring gene semaphorin 3D Neighboring gene heat shock protein family A (Hsp70) member 8 pseudogene 16 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18338 Neighboring gene dynein light chain LC8-type 1 pseudogene 7

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The sequence of the human genome. Venter JC, et al. Science, 2001 Feb 16. PMID 11181995

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

  • hCG2023776

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_006966.3 

    Range
    101..1445
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    84983495..84984839
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    86233326..86234670
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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