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Protein Coding Gene : Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2

Primary Identifier  MGI:1921355 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  74105
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable small GTPase binding activity. Predicted to be involved in Golgi to plasma membrane protein transport and protein localization to cell surface. Predicted to act upstream of or within protein transport. Predicted to be located in Golgi apparatus and clathrin-coated vesicle. Predicted to be active in trans-Golgi network. Is expressed in several structures, including branchial arch; liver; lung; small intestine; and white fat. Orthologous to human GGA2 (golgi associated, gamma adaptin ear containing, ARF binding protein 2).
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit complete embryonic lethality. Mice homozygous for a different gene trapped allele show decreased birth weight, hypoglycemia and partial neonatal lethality, with all remaining mice dying within the first three weeks of life. [provided by MGI curators]
  • synonyms:
  • Gga2,
  • mKIAA1080,
  • RIKEN cDNA 1200007E24 gene,
  • golgi associated, gamma adaptin ear containing, ARF binding protein 2,
  • 1200007E24Rik

Features --> Cross References

Genome

Sequence Feature Displayer

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0 CDSs

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0 Involved In Mutations

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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