PTPN20
Description
The PTPN20 (protein tyrosine phosphatase non-receptor type 20) is a protein-coding gene located on chromosome 10.
PTPN20 is also known as CT126, PTPN20A, PTPN20B, bA142I17.1, bA42B19.1.
Associated Diseases
- hereditary hyperferritinemia with congenital cataracts
- megalencephaly, autosomal dominant
- isolated ectopia lentis
- craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
- granular corneal dystrophy type I
- craniofacial conodysplasia
- early-onset non-syndromic cataract
- cataract 5 multiple types
- hypoalphalipoproteinemia, primary, 2
- megalocornea
- congenital glaucoma