CPA2
Description
The CPA2 (carboxypeptidase A2) is a protein-coding gene located on chromosome 7.
Carboxypeptidase A2 is an enzyme that in humans is encoded by the CPA2 gene. Three different forms of human pancreatic procarboxypeptidase A have been isolated. The A1 and A2 forms are monomeric proteins with different biochemical properties.
CPA2 is also known as -.
Associated Diseases
- hereditary hyperferritinemia with congenital cataracts
- female infertility due to oocyte meiotic arrest
- premature ovarian failure 19
- oocyte maturation defect 9
- hypergonadotropic hypogonadism-cataract syndrome
- female infertility due to zona pellucida defect
- isolated ectopia lentis
- granular corneal dystrophy type I
- early-onset non-syndromic cataract
- cataract 5 multiple types
