1. Gene
  2. GOLGA3 - golgin A3 Gene

GOLGA3 - golgin A3 Gene

Homo sapiens

Also known as MEA-2; GCP170

Gene ID: 2802 | Gene type: protein coding

About GOLGA3

Cytogenetic location: 12q24.33 Genomic coordinates (GRCh38): 12:132,768,914-132,829,081 (from NCBI)

This gene has 41 transcripts (splice variants), 199 orthologues and 3 paralogues. Ubiquitous expression in colon (RPKM 8.3), brain (RPKM 6.7) and 25 other tissues.

Summary

The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes a member of the golgin family of proteins which are localized to the Golgi. Its encoded protein has been postulated to play a role in nuclear transport and Golgi apparatus localization. Several alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Feb 2010]

GOLGA3 Products(9)

mRNA Protein Name
NM_001172557.2 NP_001166028.1 golgin subfamily A member 3 isoform 2
NM_001389683.1 NP_001376612.1 golgin subfamily A member 3 isoform 1
NM_001389684.1 NP_001376613.1 golgin subfamily A member 3 isoform 1
NM_001389685.1 NP_001376614.1 golgin subfamily A member 3 isoform 1
NM_001389686.1 NP_001376615.1 golgin subfamily A member 3 isoform 3
NM_001389687.1 NP_001376616.1 golgin subfamily A member 3 isoform 3
NM_001389688.1 NP_001376617.1 golgin subfamily A member 3 isoform 3
NM_001389689.1 NP_001376618.1 golgin subfamily A member 3 isoform 4
NM_005895.4 NP_005886.2 golgin subfamily A member 3 isoform 1
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
14522980 GOA
Cellular Component GO Annotation Evidence Reference Source
located in Golgi membrane IDA
IDA: Inferred from direct assay
14522980 GOA
located in cytosol IDA
IDA: Inferred from direct assay
14522980 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

golgin subfamily A member 3

Golgi membrane associated protein

Related Diseases

Diseases Alias
Smallpox

Variola

Ordinary Smallpox

Alastrim

Amaas

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary

Fanconi Anemia, Complementation Group C

Fanconi Anemia Complementation Group C

FANCC

Facc

Fac

Fa3

Fanconi Pancytopenia Type 3

Fanconi Pancytopenia, Type 3

Faces Syndrome

Facial Features , Anorexia, Cachexia, Eye And Skin Anomalies

Friedman-Goodman Syndrome

Abnormality Of The Face

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus GOLGA3 VGNC VGNC:29484
Canis familiaris GOLGA3 VGNC VGNC:41339
Felis catus GOLGA3 VGNC VGNC:62638
Mus musculus GOLGA3 MGD MGI:96958
Macaca mulatta GOLGA3 VGNC VGNC:73106
Rattus norvegicus GOLGA3 RGD RGD:1305262