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    GOLGA8H golgin A8 family member H [ Homo sapiens (human) ]

    Gene ID: 728498, updated on 17-Jun-2019

    Summary

    Official Symbol
    GOLGA8Hprovided by HGNC
    Official Full Name
    golgin A8 family member Hprovided by HGNC
    Primary source
    HGNC:HGNC:37443
    See related
    Ensembl:ENSG00000261794
    Gene type
    protein coding
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    GOLGA6L11
    Expression
    Broad expression in thyroid (RPKM 12.2), testis (RPKM 12.1) and 25 other tissues See more

    Genomic context

    See GOLGA8H in Genome Data Viewer
    Location:
    15q13.2
    Exon count:
    19
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (30604030..30617827)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (30895562..30909952)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene 15q13.2-13.3 gamma inversion proximal recombination region Neighboring gene dynamin 1 pseudogene 50 Neighboring gene ULK4 pseudogene 2 Neighboring gene uncharacterized LOC102725021 Neighboring gene 15q13 proximal microdeletion recombination region Neighboring gene RNA, 7SL, cytoplasmic 628, pseudogene Neighboring gene nonconserved acetylation island sequence 49 enhancer Neighboring gene Rho GTPase activating protein 11B Neighboring gene OTU deubiquitinase 7A pseudogene Neighboring gene proximal CHRNA7 low-copy repeat recombination region

    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

    Phenotypes

    NHGRI GWAS Catalog

    Description
    A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
    NHGRI GWA Catalog

    General gene information

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    Golgi organization IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    NOT spindle assembly IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    Component Evidence Code Pubs
    Golgi apparatus IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    Golgi cis cisterna IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    Golgi cisterna membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    cis-Golgi network IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 

    General protein information

    Preferred Names
    golgin subfamily A member 8H
    Names
    Golgin subfamily A member 8-like protein 1
    golgi autoantigen, golgin subfamily a, 6-like 11

    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.

    mRNA and Protein(s)

    1. NM_001282490.1NP_001269419.1  golgin subfamily A member 8H

      See identical proteins and their annotated locations for NP_001269419.1

      Status: INFERRED

      Source sequence(s)
      AC026150, AC091057
      Consensus CDS
      CCDS61576.1
      UniProtKB/Swiss-Prot
      P0CJ92
      Related
      ENSP00000456894.1, ENST00000566740.1
      Conserved Domains (2) summary
      pfam15070
      Location:226621
      GOLGA2L5; Putative golgin subfamily A member 2-like protein 5
      cl19219
      Location:175291
      DUF342; Protein of unknown function (DUF342)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

    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
      30604030..30617827
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 PATCHES

    Genomic

    1. NW_011332701.1 Reference GRCh38.p13 PATCHES

      Range
      2776519..2790316
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 PATCHES

    Genomic

    1. NW_012132920.1 Reference GRCh38.p13 PATCHES

      Range
      1910737..1922029 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 ALT_REF_LOCI_2

    Genomic

    1. NT_187660.1 Reference GRCh38.p13 ALT_REF_LOCI_2

      Range
      2888971..2902768
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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