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HNRNPDP2 heterogeneous nuclear ribonucleoprotein D pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 106481661, updated on 12-Oct-2019

Summary

Official Symbol
HNRNPDP2provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein D pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:48749
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 HNRNPDP2 in Genome Data Viewer
Location:
6q12
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (64631205..64631682, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene eyes shut homolog Neighboring gene Sharpr-MPRA regulatory region 10142 Neighboring gene Sharpr-MPRA regulatory region 6473 Neighboring gene transmembrane protein 98 pseudogene Neighboring gene uncharacterized LOC105377837

Genomic regions, transcripts, and products

General gene information

Other Names

  • heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) pseudogene 2

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_046039.1 

    Range
    101..578
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    64631205..64631682 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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