CCNI
Description
The CCNI (cyclin I) is a protein-coding gene located on chromosome 4.
CCNI is a human gene that encodes a protein called Cyclin-I, which is involved in the regulation of the cell cycle.
CCNI, also known as Cyclin-I, is a protein involved in the regulation of the cell cycle. It plays a crucial role in the G1/S transition, a critical checkpoint in the cell cycle.
CCNI is also known as CCNI1, CYC1, CYI.
Associated Diseases
- familial idiopathic steroid-resistant nephrotic syndrome
- familial juvenile hyperuricemic nephropathy type 1
- congenital nephrotic syndrome, Finnish type
- nail-patella-like renal disease
- nephronophthisis
- focal segmental glomerulosclerosis 7
- Dent disease
- lipoprotein glomerulopathy
- nephrotic syndrome, IIa 26
- glomerulopathy with fibronectin deposits 2
- C3 glomerulonephritis
- hypoxanthine guanine phosphoribosyltransferase partial deficiency
- nephrotic syndrome, type 4
- familial juvenile hyperuricemic nephropathy type 2
- xanthinuria type II
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
- autosomal dominant progressive nephropathy with hypertension
- nephrotic syndrome, type 22
