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GOLGA6L2 golgin A6 family like 2 [ Homo sapiens (human) ]

Gene ID: 283685, updated on 13-Aug-2022

Summary

Official Symbol
GOLGA6L2provided by HGNC
Official Full Name
golgin A6 family like 2provided by HGNC
Primary source
HGNC:HGNC:26695
See related
Ensembl:ENSG00000174450 AllianceGenome:HGNC:26695
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
CT105
Summary
Predicted to be located in cis-Golgi network. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Restricted expression toward testis (RPKM 11.8) See more
Orthologs
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Genomic context

See GOLGA6L2 in Genome Data Viewer
Location:
15q11.2
Exon count:
8
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (23439038..23447243, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (21171538..21180518, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (23684185..23692390, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370728 Neighboring gene HERC2 pseudogene 6 Neighboring gene uncharacterized LOC105370729 Neighboring gene microRNA 4508

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

General protein information

Preferred Names
golgin subfamily A member 6-like protein 2
Names
cancer/testis antigen 105
golgi autoantigen, golgin subfamily a, 6-like 2

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_001304388.2NP_001291317.1  golgin subfamily A member 6-like protein 2

    Status: VALIDATED

    Source sequence(s)
    AC073446, AC100756
    Consensus CDS
    CCDS76728.1
    UniProtKB/Swiss-Prot
    H3BMJ4, Q8N9W4
    UniProtKB/TrEMBL
    H3BMJ4
    Related
    ENSP00000454407.1, ENST00000567107.6
    Conserved Domains (2) summary
    PTZ00121
    Location:193444
    PTZ00121; MAEBL; Provisional
    PRK12678
    Location:540730
    PRK12678; transcription termination factor Rho; Provisional

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    23439038..23447243 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_047432396.1XP_047288352.1  golgin subfamily A member 6-like protein 2 isoform X1

  2. XM_047432397.1XP_047288353.1  golgin subfamily A member 6-like protein 2 isoform X2

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160017.1 Reference GRCh38.p14 PATCHES

    Range
    4384456..4393436 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    21171538..21180518 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_182561.1: Suppressed sequence

    Description
    NM_182561.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.