TTC39C
Description
The TTC39C (tetratricopeptide repeat domain 39C) is a protein-coding gene located on chromosome 18.
TTC39C is also known as C18orf17, HsT2697.
Associated Diseases
- primary familial polycythemia due to EPO receptor mutation
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- erythrocytosis, familial, 3
- erythrocytosis, familial, 6
- erythrocytosis, familial, 4
- iridocorneal endothelial syndrome
- X-linked sideroblastic anemia 1
- Rieger anomaly
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- ghosal hematodiaphyseal dysplasia
- overhydrated hereditary stomatocytosis
- dehydrated hereditary stomatocytosis
