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    GOLGA2P10 GOLGA2 pseudogene 10 [ Homo sapiens (human) ]

    Gene ID: 80154, updated on 10-Dec-2024

    Summary

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    Official Symbol
    GOLGA2P10provided by HGNC
    Official Full Name
    GOLGA2 pseudogene 10provided by HGNC
    Primary source
    HGNC:HGNC:26229
    See related
    Ensembl:ENSG00000290948 AllianceGenome:HGNC:26229
    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 prostate (RPKM 27.2), stomach (RPKM 24.8) and 22 other tissues See more
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    Genomic context

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    See GOLGA2P10 in Genome Data Viewer
    Location:
    15q25.2
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (82471477..82513999, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (80335605..80378148, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (82763613..82798399, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene UBE2Q2 pseudogene 6 Neighboring gene hESC enhancers GRCh37_chr15:82988342-82989330 and GRCh37_chr15:83127113-83127972 Neighboring gene chondroitin sulfate proteoglycan 4 pseudogene 10 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:83137289-83137789 Neighboring gene uncharacterized LOC105370926 Neighboring gene golgin A6 family like 17, pseudogene Neighboring gene dynamin 1 pseudogene 38

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

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    Related articles in PubMed

    1. mRNA expression of AgSK1, an adenocarconoma-associated antigen, in tumor tissue of patients with colorectal cancer: Quantitative RT-PCR analysis. Yokoyama K, et al. Hum Antibodies, 2003. PMID 15156102
    2. Identification of the immunoreactive peptide sequence for AgSK1, an adenocarcinoma-restricted antigen. Yasutomi J, et al. Tissue Antigens, 2000 Feb. PMID 10746788
    3. AgSK1, a novel carcinoma associated antigen. Chang HR, et al. Cancer Res, 1993 Mar 1. PMID 8439957
    4. Systematic identification of pathological lamin A interactors. Dittmer TA, et al. Mol Biol Cell, 2014 May. PMID 24623722, Free PMC Article
    5. A germline-specific class of small RNAs binds mammalian Piwi proteins. Girard A, et al. Nature, 2006 Jul 13. PMID 16751776

    See all (14) citations in PubMed

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Other Names

    • antigen SK1, colon cancer-associated
    • golgin A2 pseudogene 10
    • golgin subfamily A member 2-like

    Clone Names

    • FLJ17811, FLJ18166, FLJ22795, FLJ90297, FLJ99461, FLJ99773

    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_026811.3 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) includes an additional internal exon in the 5' region, and uses an alternate splice site in the 3' terminal exon, compared to variant 2.
      Source sequence(s)
      BC065260, BM981202, BQ232584, DB070142
      Related
      ENST00000795814.1

    2. NR_033936.3 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) represents the longest transcript.
      Source sequence(s)
      AC245033, AK309732, BC065260, BM981202, BQ232584, DB070142
      Related
      ENST00000618267.5

    3. NR_103496.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) uses alternate splice sites in both the 5' and 3' terminal exons, compared to variant 2.
      Source sequence(s)
      AK310769, BC065260, BM981202, BQ232584, DB070142
      Related
      ENST00000795817.1

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

      Range
      82471477..82513999 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187606.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      260554..303332 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060939.1 Alternate T2T-CHM13v2.0

      Range
      80335605..80378148 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_025084.1: Suppressed sequence

      Description
      NM_025084.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
    Nucleotide Protein
    Heading Accession and Version

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