C20orf96
Description
The C20ORF96 (chromosome 20 open reading frame 96) is a protein-coding gene located on chromosome 20.
C20ORF96 is also known as dJ1103G7.2.
Associated Diseases
- Lynch syndrome
- colorectal cancer, susceptibility to, 3
- Hirschsprung disease
- familial adenomatous polyposis 2
- AXIN2-related attenuated familial adenomatous polyposis
- anal canal carcinoma
- hereditary mixed polyposis syndrome
- Lynch syndrome 8
- chronic intestinal pseudoobstruction
- colorectal cancer, susceptibility to, 10
- duodenal atresia
- familial visceral myopathy
- inflammatory bowel disease 30
- NK-cell enteropathy