NBN
Primary Info
Mutation
Mouse studies
DNA sequencing


mRNA IDs Primary Information
NM_001024688.1,NM_002485.4 Gene Symbol NBN
Protein Name Nibrin
Alternate Names AT-V1, AT-V2, ATV, FLJ10155, MGC87362, NBS, NBS1
Gene Locus 8q21

External links
IDR HPRD OMIM Entrez Gene NetPath Reactome PDB HGNC Ensembl Swiss-Prot RefDIC
88 04050 602667 4683 NetPath_M4683 4683 -
7652 ENSG00000104320 O60934 NBN

Disease name Characteristic / Associated features Category inheritance type
Nijmegen breakage syndrome Microcephaly; microgenia; bird-like facies; prenatal growth deficiency; lymphoma; ionizing radiation sensitivity; chromosomal instability; recurrent respiratory tract infections; solid tumors; short stature; mastoiditis; sloping forehead; micrognathia; prominent midface; upslanting palpebral fissures; large, dysplastic ears; otitis media; choanal atresia or stenosis; long nose; cleft lip; cleft palate; sinusitis; bronchitis; bronchiectasis; recurrent pneumonia; diarrhea; gastrointestinal infections; anal stenosis; hydronephrosis; recurrent urinary tract infections; cafe-au-lait spots; depigmented spots; progressive vitiligo; normal IQ in infancy, then IQ drops with age; mental retardation by the age of 7 years; hyperactivity; primary ovarian failure; autoimmune hemolytic anemia; thrombocytopenia post hemolytic anemia; dysgammaglobulinemia; mild to moderately reduced T cell count; relatively increased number of natural killer cells; glioma; medulloblastoma; rhabdomyosarcoma; normal alpha fetoprotein; low T cell count; low B cell count; low CD4+ count; low CD4+/CD8+ ratio Other Well-defined Immunodeficiency Syndromes Autosomal recessive