FAM217B
Description
The FAM217B (family with sequence similarity 217 member B) is a protein-coding gene located on chromosome 20.
FAM217B is also known as C20orf177, dJ551D2.5.
Associated Diseases
- hereditary hyperferritinemia with congenital cataracts
- juvenile cataract-microcornea-renal glucosuria syndrome
- galactokinase deficiency
- Dent disease
- renal hypomagnesemia 5 with ocular involvement
- renal hypomagnesemia 2
- dicarboxylic aminoaciduria
- hemochromatosis type 5
- Fanconi renotubular syndrome 1
