GSTA2 - glutathione S-transferase alpha 2 Gene

Also Known as GST2; GTA2; GTH2; GSTA2-2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2939

About GSTA2

Cytogenetic location: 6p12.2 Genomic coordinates (GRCh38): 6:52,750,087-52,763,475 (from NCBI)

This gene has 1 transcript (splice variant), 128 orthologues and 11 paralogues. Biased expression in liver (RPKM 492.6), kidney (RPKM 310.5) and 6 other tissues.

Summary

Cytosolic and membrane-bound forms of Glutathione S-transferase are encoded by two distinct supergene families. These Enzymes function in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding these Enzymes are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of some drugs. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-tranferase belonging to the alpha class. The alpha class genes, located in a cluster mapped to chromosome 6, are the most abundantly expressed glutathione S-transferases in liver. In addition to metabolizing bilirubin and certain anti-cancer drugs in the liver, the alpha class of these Enzymes exhibit Glutathione Peroxidase activity thereby protecting the cells from Reactive Oxygen Species and the products of peroxidation. [provided by RefSeq, Jul 2008]

GSTA2 Products (1)

mRNA Protein Name
NM_000846.5 NP_000837.3 glutathione S-transferase A2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence References Source
involved in epithelial cell differentiation IEP
IEP: Inferred from expression pattern
21492153 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

GSTA2 Protein Structure

GST_N

GST_N: Glutathione S-transferase, N-terminal domain (6 - 76)

GST_C

GST_C: Glutathione S-transferase, C-terminal domain (101 - 192)

  • 0
  • 100
  • 200
  • 222 a.a.
Protein Preferred Names Protein Names

glutathione S-transferase A2

  • GST HA subunit 2

GSTA2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
GSTA2 P09210 GSTA5 Homo sapiens Q7RTV2 28514442
Intra
GSTA2 P09210 GSTA5 Homo sapiens Q7RTV2 32296183
Intra
GSTA2 P09210 GSTA5 Homo sapiens Q7RTV2 32296183
Intra
GSTA2 P09210 GSTA5 Homo sapiens Q7RTV2 32296183
Intra
GSTA2 P09210 GSTA5 Homo sapiens Q7RTV2 33961781
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25910212
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 33961781
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25910212
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25416956
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 28514442
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25416956
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 32296183
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25416956
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 32296183
Intra
GSTA2 P09210 GSTA4 Homo sapiens O15217 25910212
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Osteogenesis Imperfecta, Type I
  • Osteogenesis Imperfecta Type I

  • OI1

  • Oi, Type I

  • Osteogenesis Imperfecta Tarda

  • Osteogenesis Imperfecta With Blue Sclerae

  • Osteogenesis Imperfecta Type 1

  • Adair-Dighton Syndrome

  • Mild Osteogenesis Imperfecta

  • Non-Deforming Osteogenesis Imperfecta

  • Oi Type 1

  • Van Der Hoeve Syndrome

  • Classic Non-Deforming Oi With Blue Sclerae

  • Osteogenesis Imperfecta 1

  • Oi-I

  • Osteopenic Non-Fracture Syndrome

  • Osteogenesis Imperfecta, Mild

  • Osteogenesis Imperfecta

  • Lobstein'S Disease

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
Rattus norvegicus GSTA2 RGD RGD:2754
Others GSTA2 NCBI