HMGN5
Description
The HMGN5 (high mobility group nucleosome binding domain 5) is a protein-coding gene located on chromosome X.
HMGN5 is also known as NBP-45, NSBP1.
Associated Diseases
- urinary bladder carcinoma
- nonpapillary renal cell carcinoma
- glioblastoma
- agammaglobulinemia 10, autosomal dominant
- immunodeficiency 18
- isolated agammaglobulinemia
- severe combined immunodeficiency due to CTPS1 deficiency
- common variable immunodeficiency
- severe combined immunodeficiency due to CARD11 deficiency
- immunodeficiency 62
- immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
- severe combined immunodeficiency due to LAT deficiency
- agammaglobulinemia 7, autosomal recessive
- hyper-IgM syndrome type 3
- T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
- immunodeficiency 25
- autoimmune lymphoproliferative syndrome type 2B
- immunodeficiency, common variable, 4
- autoimmune lymphoproliferative syndrome type 4
- immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias
- combined immunodeficiency due to moesin deficiency
