PTMS
Description
The PTMS (parathymosin) is a protein-coding gene located on chromosome 12.
PTMS refers to the human gene encoding the protein parathymosin.
Parathymosin plays a role in immune regulation by counteracting the effects of prothymosin alpha. This interaction may contribute to susceptibility to certain opportunistic infections.
PTMS is also known as ParaT.
Associated Diseases
- hypomagnesemia, seizures, and intellectual disability 2
- Potocki-Lupski syndrome
- Dent disease
- nephrogenic syndrome of inappropriate antidiuresis
- hypercalcemia, infantile, 2
- hypoparathyroidism, familial isolated 1
- Dent disease type 2
- hyperprolinemia type 1
- histidinemia
- Hartnup disease
- renal hypomagnesemia 2
- phenylketonuria
