TMEM37
Description
The TMEM37 (transmembrane protein 37) is a protein-coding gene located on chromosome 2.
TMEM37 is believed to stabilize the calcium channel in an inactive (closed) state. It can modulate calcium current when expressed together with CACNA1G.
TMEM37 is also known as PR, PR1.
Associated Diseases
- Crigler-Najjar syndrome type 2
- schizophrenia
- sarcosinemia
- maple syrup urine disease
- transient familial neonatal hyperbilirubinemia
- methylmalonic acidemia due to transcobalamin receptor defect
- gluthathione peroxidase deficiency
- Rotor syndrome
- Dubin-Johnson syndrome
- hypercholanemia, familial, 2
- hemolytic anemia due to glutathione reductase deficiency
- Pallister-Hall syndrome
- neonatal intrahepatic cholestasis due to citrin deficiency
- Crigler-Najjar syndrome type 1
