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GOLGA2P7 GOLGA2 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 388152, updated on 12-Oct-2019

Summary

Official Symbol
GOLGA2P7provided by HGNC
Official Full Name
GOLGA2 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:49516
See related
Ensembl:ENSG00000225151
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Broad expression in stomach (RPKM 21.1), prostate (RPKM 19.5) and 24 other tissues See more

Genomic context

See GOLGA2P7 in Genome Data Viewer
Location:
15q25.2
Exon count:
7
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (84198848..84230168, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (84867600..84898920, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene ubiquitin conjugating enzyme E2 Q2 like Neighboring gene chondroitin sulfate proteoglycan 4 pseudogene 11 Neighboring gene chondroitin sulfate proteoglycan 4 pseudogene Neighboring gene RNA, 7SL, cytoplasmic 331, pseudogene Neighboring gene uncharacterized LOC105376724 Neighboring gene golgin A6 family like 4 Neighboring gene ubiquitin conjugating enzyme E2 Q2 pseudogene 8

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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.

RNA

  1. NR_027001.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC136698
    Related
    ENST00000400817.7

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_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    84198848..84230168 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_203426.1: Suppressed sequence

    Description
    NM_203426.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
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