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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 | B4DRA7 | 1QH3 1QH5 2F50 1QH3 1QH5 2F50 | --- |
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 |
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