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Details of HAGH gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| HAGH | GLO2,HAGH1 | Q16775 | GLO2_HUMAN | 3029
| ENSG00000063854
| Hydroxyacylglutathione hydrolase, mitochondrial | SPROT |
Phenotypes
Abnormality of blood and blood-forming tissues, Abnormality of carbohydrate metabolism/homeostasis, Abnormality of erythrocytes, Abnormality of metabolism/homeostasis, Abnormality of the nervous system, All, Autosomal dominant inheritance, Elliptocytosis, Glyoxalase deficiency, Mode of inheritance, Phenotypic abnormality, Poikilocytosis.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
|
