TVP23B
Description
The TVP23B (trans-golgi network vesicle protein 23 homolog B) is a protein-coding gene located on chromosome 17.
TVP23B is also known as CGI-148, FAM18B, FAM18B1, NPD008, YDR084C.
Associated Diseases
- inflammatory bowel disease 30
- inflammatory bowel disease 1
- Hirschsprung disease
- congenital sucrase-isomaltase deficiency
- bile acid malabsorption, primary, 1
- familial visceral myopathy
- immunodeficiency due to MASP-2 deficiency
- chronic diarrhea due to glucoamylase deficiency
- microvillus inclusion disease
- congenital short bowel syndrome
- congenital diarrhea 7 with exudative enteropathy
