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HNRNPA1P16 heterogeneous nuclear ribonucleoprotein A1 pseudogene 16 [ Homo sapiens (human) ]

Gene ID: 440396, updated on 13-Feb-2019

Summary

Official Symbol
HNRNPA1P16provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A1 pseudogene 16provided by HGNC
Primary source
HGNC:HGNC:39134
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See HNRNPA1P16 in Genome Data Viewer
Location:
17p13.3
Annotation release Status Assembly Chr Location
109 current GRCh38.p12 (GCF_000001405.38) 17 NC_000017.11 (2306762..2308048)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (2210049..2211340)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene SMG6 nonsense mediated mRNA decay factor Neighboring gene heart enhancer 8 Neighboring gene uncharacterized LOC101927839 Neighboring gene serine racemase Neighboring gene small nucleolar RNA, C/D box 91B Neighboring gene small nucleolar RNA, C/D box 91A Neighboring gene TSR1 ribosome maturation factor

Genomic regions, transcripts, and products

Bibliography

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

NCBI Reference Sequences (RefSeq)

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_009621.2 

    Range
    101..1387
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p12 Primary Assembly

    Range
    2306762..2308048
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_002943.1: Suppressed sequence

    Description
    NR_002943.1: This RefSeq was permanently suppressed because there is insufficient evidence that this locus is transcribed.
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