C11orf86
Description
The C11ORF86 (chromosome 11 open reading frame 86) is a protein-coding gene located on chromosome 11.
C11ORF86 is also known as FACI.
Associated Diseases
- glycogen storage disease VI
- obesity due to melanocortin 4 receptor deficiency
- coronary artery disease, autosomal dominant 2
- hypoinsulinemic hypoglycemia and body hemihypertrophy
- CIDEC-related familial partial lipodystrophy
- neonatal intrahepatic cholestasis due to citrin deficiency
- glycogen storage disease due to liver phosphorylase kinase deficiency
- LIPE-related familial partial lipodystrophy
- glycogen storage disease III
- glycogen storage disease IXb
- MPI-congenital disorder of glycosylation
- obesity due to prohormone convertase I deficiency
- PLIN1-related familial partial lipodystrophy
- glycogen storage disease IXa1
- autosomal recessive hyperinsulinism due to Kir6.2 deficiency
