TCAF2
Description
The TCAF2 (TRPM8 channel associated factor 2) is a protein-coding gene located on chromosome 7.
TCAF2 is also known as FAM115C, FAM139A, GATD9, GATD9B.
Associated Diseases
- beta-thalassemia-X-linked thrombocytopenia syndrome
- primary familial polycythemia due to EPO receptor mutation
- hemoglobin D disease
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- dehydrated hereditary stomatocytosis
- dominant beta-thalassemia
- hemoglobin H disease
- hemoglobin E disease
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin C-beta-thalassemia syndrome
- gamma-glutamylcysteine synthetase deficiency
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- overhydrated hereditary stomatocytosis
- erythroleukemia, familial, susceptibility to
- familial isolated congenital asplenia
- cryohydrocytosis
- combined immunodeficiency due to OX40 deficiency
- immunodeficiency 75
- congenital dyserythropoietic anemia type 2
