NUP62CL
Description
The NUP62CL (nucleoporin 62 C-terminal like) is a protein-coding gene located on chromosome X.
NUP62CL is also known as -.
Associated Diseases
- hemolytic anemia due to glutathione reductase deficiency
- granular corneal dystrophy type I
- X-linked endothelial corneal dystrophy
- lattice corneal dystrophy type I
- granular corneal dystrophy type II
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- megaloblastic anemia, folate-responsive
- corneal endothelial dystrophy
- hypoparathyroidism, familial isolated, 2
- Thiel-Behnke corneal dystrophy
- macular corneal dystrophy
- elliptocytosis 2