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PTP4A2P2 PTP4A2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 5769, updated on 12-Oct-2019

Summary

Official Symbol
PTP4A2P2provided by HGNC
Official Full Name
PTP4A2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:9638
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PTP4AP2

Genomic context

See PTP4A2P2 in Genome Data Viewer
Location:
11q25
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (134123130..134125202, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (133993322..133995113, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2731 Neighboring gene junctional adhesion molecule 3 Neighboring gene uncharacterized LOC107984040 Neighboring gene small nucleolar RNA, C/D box 153 Neighboring gene non-SMC condensin II complex subunit D3 Neighboring gene zinc finger protein 628 pseudogene

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • protein tyrosine phosphatase IVA pseudogene 2
  • protein tyrosine phosphatase type IVA pseudogene 2
  • protein tyrosine phosphatase type IVA, member 2 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_001182.7 

    Range
    101..2173
    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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    134123130..134125202 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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