PSG7
Description
The PSG7 (pregnancy specific beta-1-glycoprotein 7) is a protein-coding gene located on chromosome 19.
PSG7 is also known as PS-beta-G-7, PSBG-7, PSG1, PSGGA.
Associated Diseases
- obesity due to melanocortin 4 receptor deficiency
- LIPE-related familial partial lipodystrophy
- obesity due to leptin receptor gene deficiency
- PLIN1-related familial partial lipodystrophy
- CIDEC-related familial partial lipodystrophy
- AXIN2-related attenuated familial adenomatous polyposis
- obesity due to prohormone convertase I deficiency
- obesity due to pro-opiomelanocortin deficiency
- obesity due to congenital leptin deficiency
- Muir-Torre syndrome
- short stature due to primary acid-labile subunit deficiency
- AKT2-related familial partial lipodystrophy
- familial partial lipodystrophy, Kobberling type
- familial partial lipodystrophy, Dunnigan type
- Hirschsprung disease
- PPARG-related familial partial lipodystrophy
- severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
