TMEM11
Description
The TMEM11 (transmembrane protein 11) is a protein-coding gene located on chromosome 17.
TMEM11 contributes to the shaping and organization of mitochondria.
TMEM11 is also known as C17orf35, PM1, PMI.
Associated Diseases
- left ventricular noncompaction
- hemoglobin E-beta-thalassemia syndrome
- IRIDA syndrome
- left ventricular noncompaction 10
- dilated cardiomyopathy 1GG
- hemoglobin D disease
- Rh deficiency syndrome
- dilated cardiomyopathy 1AA
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- sick sinus syndrome 2, autosomal dominant
- long QT syndrome 15
- overhydrated hereditary stomatocytosis
- congenital heart block
- atrial standstill
