ITFG1
Description
The ITFG1 (integrin alpha FG-GAP repeat containing 1) is a protein-coding gene located on chromosome 16.
ITFG1 is a modulator of T-cell function, potentially playing a protective role in graft versus host disease.
ITFG1 is also known as 2310047C21Rik, CDA08, LINKIN, LNKN-1, TIP.
Associated Diseases
- glycogen storage disease IXb
- graft versus host disease
- schizophrenia
- glycogen storage disease VI
- type 1 diabetes mellitus
