INTS3
Description
The INTS3 (integrator complex subunit 3) is a protein-coding gene located on chromosome 1.
Integrator complex subunit 3 is a protein that in humans is encoded by the INTS3 gene.
INTS3 is also known as C1orf193, C1orf60, INT3, SOSS-A, SOSSA.
Associated Diseases
- myoepithelial tumor
- prostate cancer
- hemoglobin D disease
- primary familial polycythemia due to EPO receptor mutation
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- dominant beta-thalassemia
- hemoglobin E disease
- hemoglobin E-beta-thalassemia syndrome
- delta-beta-thalassemia
- hemoglobin C-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- dehydrated hereditary stomatocytosis
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- erythrocytosis, familial, 6
- erythrocytosis, familial, 3