GIMAP1
Description
The GIMAP1 (GTPase, IMAP family member 1) is a protein-coding gene located on chromosome 7.
GIMAP1 is also known as HIMAP1, IAN2, IMAP1, IMAP38.
Associated Diseases
- common variable immunodeficiency
- isolated agammaglobulinemia
- combined immunodeficiency with skin granulomas
- classic Hodgkin lymphoma
- immunodeficiency 18
- severe combined immunodeficiency due to CARD11 deficiency
- severe combined immunodeficiency due to CTPS1 deficiency
- BENTA disease
- severe combined immunodeficiency due to IKK2 deficiency
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
- immunodeficiency 62
- hyper-IgM syndrome type 3
- immunodeficiency 105
- immunodeficiency, common variable, 4
- agammaglobulinemia 10, autosomal dominant
- immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias
- immunodeficiency, common variable, 14
- immunodeficiency 72 with autoinflammation
- short-limb skeletal dysplasia with severe combined immunodeficiency
- combined immunodeficiency due to moesin deficiency
