HMCN2
Description
The HMCN2 (hemicentin 2) is a protein-coding gene located on chromosome 9.
Hemicentin 2 is a protein that in humans is encoded by the HMCN2 gene.
HMCN2 is also known as -.
Associated Diseases
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- primary familial polycythemia due to EPO receptor mutation
- hemoglobin D disease
- alpha thalassemia-intellectual disability syndrome type 1
- delta-beta-thalassemia
- hemoglobin E-beta-thalassemia syndrome
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- dominant beta-thalassemia
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin C-beta-thalassemia syndrome
- erythrocytosis, familial, 3
- X-linked sideroblastic anemia 1
- erythrocytosis, familial, 6
- hemoglobin E disease
