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GOLGA7B golgin A7 family member B [ Homo sapiens (human) ]

Gene ID: 401647, updated on 22-Aug-2020

Summary

Official Symbol
GOLGA7Bprovided by HGNC
Official Full Name
golgin A7 family member Bprovided by HGNC
Primary source
HGNC:HGNC:31668
See related
Ensembl:ENSG00000155265 MIM:614189
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
C10orf132; C10orf133; bA459F3.4; bA451M19.3
Expression
Biased expression in brain (RPKM 7.2), skin (RPKM 7.1) and 11 other tissues See more
Orthologs

Genomic context

See GOLGA7B in Genome Data Viewer
Location:
10q24.2
Exon count:
5
Annotation release Status Assembly Chr Location
109.20200815 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (97849843..97871578)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (99609995..99631335)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 10024 Neighboring gene uncharacterized LOC107984260 Neighboring gene long intergenic non-protein coding RNA 866 Neighboring gene cartilage acidic protein 1 Neighboring gene Sharpr-MPRA regulatory region 340 Neighboring gene microRNA 3085

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

Associated conditions

Description Tests
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
GeneReviews: Not available

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • FLJ43465, MGC131701

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enzyme binding IPI
Inferred from Physical Interaction
more info
PubMed 
protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
contributes_to protein-cysteine S-palmitoyltransferase activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
peptidyl-L-cysteine S-palmitoylation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
protein targeting to membrane IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
Golgi membrane IEA
Inferred from Electronic Annotation
more info
 
palmitoyltransferase complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

General protein information

Preferred Names
golgin subfamily A member 7B
Names
golgi autoantigen, golgin subfamily a, 7B

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_001010917.3NP_001010917.1  golgin subfamily A member 7B

    See identical proteins and their annotated locations for NP_001010917.1

    Status: VALIDATED

    Source sequence(s)
    AK125454, AL358938, AW172573, BC008047, BC110810, BI754792, BM713854, BQ950672, CA308047, DN831741
    Consensus CDS
    CCDS31265.1
    UniProtKB/Swiss-Prot
    Q2TAP0
    UniProtKB/TrEMBL
    Q6ZUQ1
    Related
    ENSP00000359634.1, ENST00000370602.6
    Conserved Domains (1) summary
    pfam10256
    Location:21133
    Erf4; Golgin subfamily A member 7/ERF4 family

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20200815

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    97849843..97871578
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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