HAGH
Hydroxyacylglutathione hydrolase, mitochondrial
Also known as: GLO2, GLO2_HUMAN, GLXII, HAGH1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16775
- Gene
- HAGH
- Ensembl
- ENSG00000063854
- Chromosome
- 16
- Canonical length
- 308 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
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. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]
Canonical amino-acid sequenceUniProt
308 residues, UniProt reviewed canonical sequence.
>Q16775|HAGH
1 MVVGRGLLGR RSLAALGAAC ARRGLGPALL GVFCHTDLRK NLTVDEGTMK VEVLPALTDN
61 YMYLVIDDET KEAAIVDPVQ PQKVVDAARK HGVKLTTVLT THHHWDHAGG NEKLVKLESG
121 LKVYGGDDRI GALTHKITHL STLQVGSLNV KCLATPCHTS GHICYFVSKP GGSEPPAVFT
181 GDTLFVAGCG KFYEGTADEM CKALLEVLGR LPPDTRVYCG HEYTINNLKF ARHVEPGNAA
241 IREKLAWAKE KYSIGEPTVP STLAEEFTYN PFMRVREKTV QQHAGETDPV TTMRAVRREK
301 DQFKMPRDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HAGH can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 221 nTPM
Expression across tissuesHPA
Tissue
- liver: 221 nTPM
- skeletal muscle: 188 nTPM
- tongue: 146 nTPM
- heart muscle: 130 nTPM
- adrenal gland: 107 nTPM
- cerebral cortex: 107 nTPM
Single-cell type
- late primary spermatocytes: 429 nCPM
- oocytes: 281 nCPM
- hepatocytes: 232 nCPM
- early spermatids: 227 nCPM
- enterocytes: 190 nCPM
- erythrocytes: 183 nCPM
Immune cell
- non-classical monocyte: 89 nTPM
- eosinophil: 65 nTPM
- plasmacytoid DC: 65 nTPM
- intermediate monocyte: 59 nTPM
- T-reg: 43 nTPM
- basophil: 37 nTPM
Brain region
- hippocampal formation: 88 nTPM
- cerebral cortex: 85 nTPM
- white matter: 81 nTPM
- thalamus: 77 nTPM
- hypothalamus: 75 nTPM
- pons: 75 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.12
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glutathione biosynthetic process
- glutathione metabolic process
- methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HAGH as an antibody target. Whether an autoantibody or antibody against HAGH could matter depends on whether native HAGH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HAGH is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label HAGH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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