Format

Send to:

Choose Destination

HNRNPA3P1 heterogeneous nuclear ribonucleoprotein A3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 10151, updated on 24-Jul-2021

Summary

Official Symbol
HNRNPA3P1provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:13729
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FBRNP; HNRPA3; D10S102; HNRPA3P1
Summary
This locus shares sequence similarity with heterogeneous nuclear ribonuclear proteins and represents an apparent transcribed pseudogene of the HNRPA3 gene, which maps to chromosome 2. [provided by RefSeq, Jul 2008]
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See HNRNPA3P1 in Genome Data Viewer
Location:
10q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (43787412..43790417, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (44282860..44285865, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene elongin C pseudogene 30 Neighboring gene uncharacterized LOC105378275 Neighboring gene long intergenic non-protein coding RNA 2658 Neighboring gene uncharacterized protein C10orf142-like Neighboring gene long intergenic non-protein coding RNA 619

Genomic regions, transcripts, and products

Phenotypes

Associated conditions

Description Tests
Genome-wide association study link novel loci to endometriosis.
GeneReviews: Not available

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

RNA

  1. NR_002726.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL355989

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    43787412..43790417 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_005758.1: Suppressed sequence

    Description
    NM_005758.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
Support Center