Gene: NHEJ1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79840
Gene Symbol: NHEJ1
NHEJ1 		0.140 GeneticVariation disease BEFREE Patients with XLF mutation exhibit microcephaly, lymphopenia, and growth retardation, and are immunodeficient and radiosensitive. 28846869 2017
Entrez Id: 79840
Gene Symbol: NHEJ1
NHEJ1 		0.140 Biomarker disease BEFREE Microcephaly and immunodeficiency are common to DNA ligase IV deficiency (LIG4 syndrome) and severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation due to NHEJ1 deficiency (NHEJ1 syndrome). 22373003 2012
Entrez Id: 79840
Gene Symbol: NHEJ1
NHEJ1 		0.140 GeneticVariation disease BEFREE Cernunnos/XLF is a recently identified NHEJ gene which is mutated in immunodeficiency with microcephaly patients. 19223975 2009
Entrez Id: 79840
Gene Symbol: NHEJ1
NHEJ1 		0.140 GeneticVariation disease BEFREE The NHEJ1 gene was recently identified as being responsible for autosomal recessive immunodeficiency with microcephaly. 17191205 2007
Entrez Id: 79840
Gene Symbol: NHEJ1
NHEJ1 		0.140 Biomarker disease HPO