HAGH

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Hydroxyacylglutathione hydrolase, mitochondrial is an enzyme that in humans is encoded by the HAGH gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesHAGH, GLO2, GLX2, GLXII, HAGH1, hydroxyacylglutathione hydrolase
Quick facts Available structures, PDB ...
HAGH
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesHAGH, GLO2, GLX2, GLXII, HAGH1, hydroxyacylglutathione hydrolase
External IDsOMIM: 138760; MGI: 95745; HomoloGene: 3890; GeneCards: HAGH; OMA:HAGH - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001040427
NM_001286249
NM_005326
NM_001363912
NM_001363914

NM_001159626
NM_024284

RefSeq (protein)

NP_001035517
NP_001273178
NP_005317
NP_001350841
NP_001350843

NP_001153098
NP_077246

Location (UCSC)Chr 16: 1.8 – 1.83 MbChr 17: 25.06 – 25.08 Mb
PubMed search[3][4]
Wikidata
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The enzyme encoded by this gene is classified as a thiolesterase and is responsible for the hydrolysis of S-lactoyl-glutathione to reduced glutathione and D-lactate.[7]

References

Further reading

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