Gene: MAD2L1BP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 GeneticVariation disease BEFREE Exome sequencing and linkage analysis were utilized to investigate a large Taiwanese family with a dominantly inherited adult-onset motor and sensory axonal neuropathy in which mutations in common CMT2-implicated genes had been previously excluded. 25098539 2014
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 GeneticVariation disease BEFREE Recognition that mutations in MT-ATP6 cause CMT2 enhances current understanding of the pathogenic basis of axonal neuropathy. 22933740 2012
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 Biomarker disease BEFREE Charcot-Marie-Tooth neuropathy type 2 (CMT2) is an axonal neuropathy, also of undetermined cause. 11345007 2001
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 Biomarker disease BEFREE Charcot-Marie-Tooth neuropathy type 2 (CMT2) is an axonal neuropathy, also of undetermined cause. 10219749 1999
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 GeneticVariation disease BEFREE Charcot-Marie-Tooth neuropathy type 2 (CMT2) is a common inherited axonal neuropathy. 8614538 1996
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 GeneticVariation disease BEFREE CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy. 7573046 1995
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 Biomarker disease BEFREE Charcot-Marie-Tooth neuropathy type II (CMT2) is an axonal neuropathy, also of undetermined cause. 7849745 1994
Entrez Id: 9587
Gene Symbol: MAD2L1BP
MAD2L1BP 		0.080 Biomarker disease BEFREE CMT2 is an axonal neuropathy of undetermined cause. 7804455 1994