ZNF496
Description
The ZNF496 (zinc finger protein 496) is a protein-coding gene located on chromosome 1.
ZNF496 acts as a DNA-binding transcription factor, capable of both activating and repressing gene expression.
ZNF496 is also known as NIZP1, ZFP496, ZKSCAN17, ZSCAN49.
Associated Diseases
- beta-thalassemia-X-linked thrombocytopenia syndrome
- macrothrombocytopenia, isolated, 2, autosomal dominant
- thrombocytopenia 4
- thrombocytopenia 7
- autosomal dominant macrothrombocytopenia
- erythroleukemia, familial, susceptibility to
- thrombocytopenia, anemia, and myelofibrosis
- platelet-type bleeding disorder 9
- platelet-type bleeding disorder 15
- X-linked sideroblastic anemia 1
- thrombocytopenia 2
- monosomy 7 myelodysplasia and leukemia syndrome 1
- bleeding disorder, platelet-type, 24
- platelet-type von Willebrand disease
- platelet-type bleeding disorder 10
- familial isolated congenital asplenia
