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Details of GLRX5 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| GLRX5 | C14orf87 | Q86SX6 | GLRX5_HUMAN | 51218
| Q86WY3
| Q8IZ54 | mitochondrial |
Phenotypes
Abnormality of blood and blood-forming tissues, Abnormality of cation homeostasis, Abnormality of erythrocytes, Abnormality of ion homeostasis, Abnormality of iron homeostasis, Abnormality of metabolism/homeostasis, Abnormality of transition element cation homeostasis, Age of onset, All, Anemia, Autosomal recessive inheritance, Heterogeneous, Increased serum ferritin, Infantile onset, Mode of inheritance, Onset, Onset and clinical course, Phenotypic abnormality.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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