TMEM256
Description
The TMEM256 (transmembrane protein 256) is a protein-coding gene located on chromosome 17.
TMEM256 is also known as C17orf61.
Associated Diseases
- short rib-polydactyly syndrome, Majewski type
- asphyxiating thoracic dystrophy 3
- hemoglobin D disease
- ghosal hematodiaphyseal dysplasia
- Weismann-Netter syndrome
- hemoglobin E disease
- hypertrophic cardiomyopathy 6
- dominant beta-thalassemia
- familial sick sinus syndrome
- Brugada syndrome
- fibular hemimelia
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- metaphyseal dysplasia, Braun-Tinschert type
- Jervell and Lange-Nielsen syndrome
- Eiken syndrome
- hemoglobin E-beta-thalassemia syndrome
