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DSTNP2 DSTN pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 171220, updated on 25-Oct-2022

Summary

Official Symbol
DSTNP2provided by HGNC
Official Full Name
DSTN pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:34546
See related
Ensembl:ENSG00000290712 AllianceGenome:HGNC:34546
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See DSTNP2 in Genome Data Viewer
Location:
12p13.31
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (6884682..6885786)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (6893944..6895049)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (6993846..6994950)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene triosephosphate isomerase 1 Neighboring gene uncharacterized LOC105369632 Neighboring gene splA/ryanodine receptor domain and SOCS box containing 2 Neighboring gene ribosomal protein L13 pseudogene 5 Neighboring gene leucine rich repeat containing 23 Neighboring gene enolase 2 Neighboring gene uncharacterized LOC124902868

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • destrin, actin depolymerizing factor pseudogene 2
  • destrin-2 pseudogene

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.

RNA

  1. NR_033796.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BM993550, U47924
    Related
    ENST00000602547.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    6884682..6885786
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    6893944..6895049
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)