SAMD3
Description
The SAMD3 (sterile alpha motif domain containing 3) is a protein-coding gene located on chromosome 6.
SAMD3 is also known as -.
Associated Diseases
- schizophrenia
- coronary atherosclerosis
- Okt4 epitope deficiency
- combined immunodeficiency with skin granulomas
- severe combined immunodeficiency due to IKK2 deficiency
- neutropenia, severe congenital, 2, autosomal dominant
- immunodeficiency 19
- 22q11.2 deletion syndrome
- immunodeficiency 18
- agammaglobulinemia 7, autosomal recessive
- epidermodysplasia verruciformis
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- common variable immunodeficiency
- reticular dysgenesis
- T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant
- combined immunodeficiency due to partial RAG1 deficiency
- immunodeficiency 105