SLC13A1
Description
The SLC13A1 (solute carrier family 13 member 1) is a protein-coding gene located on chromosome 7.
SLC13A1 acts as a sodium:sulfate symporter, facilitating the reabsorption of sulfate in the kidneys and small intestine. It also possesses the ability to transport selenate and thiosulfate.
SLC13A1 is also known as NAS1, NaSi-1.
Associated Diseases
- cancer
- Dent disease
- autosomal dominant epilepsy with auditory features
- adenine phosphoribosyltransferase deficiency
- renal hypomagnesemia 2
- primary hyperoxaluria type 2
- galactokinase deficiency
- Fanconi renotubular syndrome 1
- developmental and epileptic encephalopathy, 9
- benign familial infantile epilepsy
- glycogen storage disease due to GLUT2 deficiency
- generalized epilepsy with febrile seizures plus, type 2
- Fuhrmann syndrome
- primary hyperoxaluria type 3
