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Details of GSS gene in Homo sapiens
Disease |
|---|
| Disease |
OMIM id |
| Glutathione synthetase deficiency (GSS deficiency) [MIM:266130]: Severe form characterized by an increased rate of hemolysis and defective function of the central nervous system. Note=The disease is caused by mutations affecting the gene represented in this entry. |
266130 |
Glutathione synthetase deficiency of erythrocytes (GLUSYNDE) [MIM:231900]: Mild form causing hemolytic anemia. Note=The disease is caused by mutations affecting the gene represented in this entry. |
231900 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Gss | | gss-1 | Sp-Gss_1 |
