PSG8
Description
The PSG8 (pregnancy specific beta-1-glycoprotein 8) is a protein-coding gene located on chromosome 19.
PSG8 is also known as PSG1.
Associated Diseases
- thyroid gland adenocarcinoma
- low grade glioma
- 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
