PSG5

• SHARE NOW |
• Tweet Opens in a new window.
• Pin it Opens in a new window.
• Share Opens in a new window.
• Share Opens in a new window.
• Email Opens in a new window.

---

Description

The PSG5 (pregnancy specific beta-1-glycoprotein 5) is a protein-coding gene located on chromosome 19.

Pregnancy-specific beta-1-glycoprotein 5 is a protein that in humans is encoded by the PSG5 gene.

PSG5 is also known as FL-NCA-3, PSG.

Associated Diseases

• thyroid gland adenocarcinoma
• ringed hair disease
• Griscelli syndrome type 3
• uncombable hair syndrome
• hyperinsulinism due to INSR deficiency
• hyperinsulinism due to glucokinase deficiency
• microcephaly-albinism-digital anomalies syndrome
• pili bifurcati
• exercise-induced hyperinsulinism
• oculocutaneous albinism type 3
• alopecia, androgenetic, 1
• wooly hair, autosomal recessive 3