PSG1
Description
The PSG1 (pregnancy specific beta-1-glycoprotein 1) is a protein-coding gene located on chromosome 19.
PSG1 may refer to:
PSG1 is also known as B1G1, CD66f, DHFRP2, FL-NCA-1/2, PBG1, PS-beta-C/D, PS-beta-G-1, PSBG-1, PSBG1, PSG95, PSGGA, PSGIIA, SP1.
Associated Diseases
- 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 pro-opiomelanocortin deficiency
- obesity due to prohormone convertase I 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
