ZNF682
Description
The ZNF682 (zinc finger protein 682) is a protein-coding gene located on chromosome 19.
ZNF682 is also known as BC39498_3.
Associated Diseases
- X-linked severe congenital neutropenia
- neutropenia, severe congenital, 2, autosomal dominant
- nonimmune chronic idiopathic neutropenia of adults
- autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- reticular dysgenesis
- pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9
- combined immunodeficiency with skin granulomas
- combined immunodeficiency due to moesin deficiency
- X-linked sideroblastic anemia 1
- neutropenia, severe congenital, 1, autosomal dominant
- 22q11.2 deletion syndrome
- agammaglobulinemia 7, autosomal recessive
- epidermodysplasia verruciformis
- monocytopenia with susceptibility to infections
- combined immunodeficiency due to partial RAG1 deficiency
- immunodeficiency 18
- short-limb skeletal dysplasia with severe combined immunodeficiency
- pancytopenia-developmental delay syndrome