TMEM14C
Description
The TMEM14C (transmembrane protein 14C) is a protein-coding gene located on chromosome 6.
TMEM14C is essential for the proper production of heme, a vital molecule in red blood cells that carries oxygen throughout the body.
TMEM14C is also known as C6orf53, HSPC194, MSTP073, NET26, bA421M1.6.
Associated Diseases
- hemoglobin D disease
- dominant beta-thalassemia
- hemoglobin H disease
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin E disease
- dehydrated hereditary stomatocytosis
- hemoglobin C-beta-thalassemia syndrome
- X-linked sideroblastic anemia 1
- hemoglobin E-beta-thalassemia syndrome
- delta-beta-thalassemia
- cyanosis, transient neonatal
- alpha-thalassemia-myelodysplastic syndrome
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- beta-thalassemia-X-linked thrombocytopenia syndrome
- microcytic anemia with liver iron overload
- Heinz body anemia
- sideroblastic anemia 3
