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HNRNPA1P60 heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 [ Homo sapiens (human) ]

Gene ID: 120364, updated on 10-Oct-2023

Summary

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Official Symbol
HNRNPA1P60provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A1 pseudogene 60provided by HGNC
Primary source
HGNC:HGNC:48790
See related
AllianceGenome:HGNC:48790
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:
11q23.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (110787700..110789058, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (110797727..110799085, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (110658423..110659781, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902753 Neighboring gene Rho GTPase activating protein 20 Neighboring gene uncharacterized LOC124902754 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:110581379-110582024 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:110583007-110583508 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr11:110703043-110704242 Neighboring gene uncharacterized LOC105369488 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_18726 Neighboring gene uncharacterized LOC105369489

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)

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_021803.4 

    Range
    101..1459
    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    110787700..110789058 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    110797727..110799085 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Chemical Information
Molecular Biology Databases