Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6314
Gene Symbol: ATXN7
ATXN7 		0.300 Biomarker phenotype CTD_human Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report. 25664129 2014
Entrez Id: 1141
Gene Symbol: CHRNB2
CHRNB2 		0.300 Therapeutic phenotype CTD_human The β2 nicotinic acetylcholine receptor subunit differentially influences ethanol behavioral effects in the mouse. 23419392 2013
Entrez Id: 5376
Gene Symbol: PMP22
PMP22 		0.300 Biomarker phenotype CTD_human Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment. 12427913 2002
Entrez Id: 7274
Gene Symbol: TTPA
TTPA 		0.300 Biomarker phenotype CTD_human Ataxia caused by mutations in the alpha-tocopherol transfer protein gene. 10896705 2000
Entrez Id: 18
Gene Symbol: ABAT
ABAT 		0.300 Biomarker phenotype CTD_human 4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency. 10407778 1999