SPRR1B
Description
The SPRR1B (small proline rich protein 1B) is a protein-coding gene located on chromosome 1.
SPRR1B is a gene that encodes for Cornifin-B protein in humans.
SPRR1B is also known as CORNIFIN, GADD33, SPR-IB, SPRR1.
Associated Diseases
- ovarian cancer
- pentosuria
- iminoglycinuria
- cystathioninuria
- phosphohydroxylysinuria
- beta-aminoisobutyric acid, urinary excretion of
- uridine-cytidineuria
- isolated sedoheptulokinase deficiency
- seizures-intellectual disability due to hydroxylysinuria syndrome
- hyperdibasic aminoaciduria type 1
- carnosinemia
- cystinuria
- histidinemia
- hyperprolinemia type 2
- dicarboxylic aminoaciduria