IFIT1B
Description
The IFIT1B (interferon induced protein with tetratricopeptide repeats 1B) is a protein-coding gene located on chromosome 10.
IFIT1B is also known as IFIT1L, bA149I23.6.
Associated Diseases
- varicella, severe recurrent
- T-B+ severe combined immunodeficiency due to JAK3 deficiency
- MHC class II deficiency
- hyper-IgM syndrome type 2
- isolated agammaglobulinemia
- immunodeficiency 66
- immunodeficiency 37
- severe combined immunodeficiency due to CARD11 deficiency
- hyper-IgM syndrome type 5
- severe combined immunodeficiency due to CTPS1 deficiency
- autoimmune lymphoproliferative syndrome type 2B
- immunodeficiency due to selective anti-polysaccharide antibody deficiency
- hyper-IgM syndrome type 3
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- type II complement component 8 deficiency
- agammaglobulinemia 10, autosomal dominant
