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HNRNPA3P8 heterogeneous nuclear ribonucleoprotein A3 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 100129557, updated on 10-Oct-2023

Summary

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Official Symbol
HNRNPA3P8provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A3 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:48497
See related
Ensembl:ENSG00000239699 AllianceGenome:HGNC:48497
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:
3p12.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (80216261..80217264)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (80270852..80271855)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (80265411..80266414)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene high mobility group box 1 pseudogene 38 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:80101631-80102130 Neighboring gene oxysterol binding protein like 9 pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chr3:80312337-80312853 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:80363655-80364154 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:80546336-80546876 Neighboring gene HYDIN pseudogene 1 Neighboring gene uncharacterized LOC105377177 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr3:80578964-80580163 Neighboring gene VISTA enhancer hs1995 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:80630216-80630977 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:80658915-80659124 Neighboring gene uncharacterized LOC124906335

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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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_029271.1 

    Range
    101..1104
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    80216261..80217264
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    80270852..80271855
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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