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    GOLGA8G golgin A8 family member G [ Homo sapiens (human) ]

    Gene ID: 283768, updated on 2-Nov-2024

    Summary

    Official Symbol
    GOLGA8Gprovided by HGNC
    Official Full Name
    golgin A8 family member Gprovided by HGNC
    Primary source
    HGNC:HGNC:25328
    See related
    Ensembl:ENSG00000183629 AllianceGenome:HGNC:25328
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    GOLGA8F
    Summary
    Predicted to be involved in Golgi organization. Predicted to be located in Golgi apparatus. Predicted to be active in Golgi cis cisterna; Golgi cisterna membrane; and cis-Golgi network. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Restricted expression toward testis (RPKM 32.3) See more
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    Genomic context

    See GOLGA8G in Genome Data Viewer
    Location:
    15q13.1
    Exon count:
    20
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (28519611..28532997, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (26296348..26309735, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (28764757..28778117, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:28737210-28737710 Neighboring gene microRNA 4509-3 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:28752889-28753390 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:28753391-28753890 Neighboring gene ABCB10 pseudogene 4 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:28777697-28778196 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:28790612-28791114 Neighboring gene MPHOSPH10 pseudogene 8 Neighboring gene golgin A6 family like 25

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues 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

    General protein information

    Preferred Names
    putative golgin subfamily A member 8G
    Names
    golgi autoantigen, golgin subfamily a, 8G
    putative golgin subfamily A member 8F/8G

    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.

    mRNA and Protein(s)

    1. NM_001350919.3NP_001337848.1  putative golgin subfamily A member 8G isoform 1

      Status: VALIDATED

      Source sequence(s)
      AC138749
      Consensus CDS
      CCDS86439.1
      UniProtKB/Swiss-Prot
      P0DX53
      UniProtKB/TrEMBL
      A0A0G2JP48, A0A0G2JPF6
      Related
      ENSP00000458130.1, ENST00000525590.3
      Conserved Domains (3) summary
      COG1196
      Location:104343
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      pfam15070
      Location:239472
      GOLGA2L5; Putative golgin subfamily A member 2-like protein 5
      pfam19046
      Location:609648
      GM130_C; GM130 C-terminal binding motif
    2. NM_001368078.2NP_001355007.1  putative golgin subfamily A member 8G isoform 2

      Status: VALIDATED

      Source sequence(s)
      AC138749
      UniProtKB/Swiss-Prot
      Q0D2H9
      Related
      ENST00000382949.7
    3. NM_001368080.2NP_001355009.1  putative golgin subfamily A member 8G isoform 3

      Status: VALIDATED

      Source sequence(s)
      AC138749
      UniProtKB/Swiss-Prot
      Q0D2H9
      Related
      ENST00000524859.5

    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
      28519611..28532997 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_024449906.2XP_024305674.1  putative golgin subfamily A member 8G isoform X3

      UniProtKB/Swiss-Prot
      Q0D2H9
      Conserved Domains (1) summary
      pfam15070
      Location:21441
      GOLGA2L5; Putative golgin subfamily A member 2-like protein 5
    2. XM_024449905.2XP_024305673.1  putative golgin subfamily A member 8G isoform X2

      UniProtKB/TrEMBL
      A0A0G2JPF6
      Conserved Domains (2) summary
      pfam15070
      Location:238658
      GOLGA2L5; Putative golgin subfamily A member 2-like protein 5
      cl25732
      Location:107351
      SMC_N; RecF/RecN/SMC N terminal domain
    3. XM_024449904.2XP_024305672.1  putative golgin subfamily A member 8G isoform X1

      UniProtKB/TrEMBL
      A0A0G2JPF6
      Conserved Domains (2) summary
      pfam15070
      Location:239659
      GOLGA2L5; Putative golgin subfamily A member 2-like protein 5
      cl25732
      Location:107352
      SMC_N; RecF/RecN/SMC N terminal domain

    RNA

    1. XR_002957634.1 RNA Sequence

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_011332701.1 Reference GRCh38.p14 PATCHES

      Range
      681620..695006 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054331760.1XP_054187735.1  putative golgin subfamily A member 8G isoform X3

    2. XM_054331759.1XP_054187734.1  putative golgin subfamily A member 8G isoform X2

    3. XM_054331758.1XP_054187733.1  putative golgin subfamily A member 8G isoform X1

    RNA

    1. XR_008485734.1 RNA Sequence

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NW_003315943.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      219191..232577 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054329576.1XP_054185551.1  putative golgin subfamily A member 8G isoform X3

    2. XM_054329575.1XP_054185550.1  putative golgin subfamily A member 8G isoform X2

    3. XM_054329574.1XP_054185549.1  putative golgin subfamily A member 8G isoform X1

    RNA

    1. XR_008485653.1 RNA Sequence

    Reference GRCh38.p14 ALT_REF_LOCI_2

    Genomic

    1. NT_187660.1 Reference GRCh38.p14 ALT_REF_LOCI_2

      Range
      795406..808792 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054330023.1XP_054185998.1  putative golgin subfamily A member 8G isoform X3

    2. XM_054330022.1XP_054185997.1  putative golgin subfamily A member 8G isoform X2

    3. XM_054330021.1XP_054185996.1  putative golgin subfamily A member 8G isoform X1

    RNA

    1. XR_008485668.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060939.1 Alternate T2T-CHM13v2.0

      Range
      26296348..26309735 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054377748.1XP_054233723.1  putative golgin subfamily A member 8G isoform X3

    2. XM_054377747.1XP_054233722.1  putative golgin subfamily A member 8G isoform X4

    3. XM_054377746.1XP_054233721.1  putative golgin subfamily A member 8G isoform X2

    4. XM_054377745.1XP_054233720.1  putative golgin subfamily A member 8G isoform X1

    RNA

    1. XR_008488941.1 RNA Sequence

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001012420.2: Suppressed sequence

      Description
      NM_001012420.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.