Gene: SETX ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23064
Gene Symbol: SETX
SETX 		0.110 GeneticVariation phenotype BEFREE Ataxia with oculomotor apraxia type 2 (AOA2) is a newly described autosomal recessive cerebellar ataxia (ARCA) defined by genetic location to 9q34 of three families sharing gait ataxia, oculomotor apraxia and/or elevated alpha-foetoprotein (AFP) levels. 14736755 2004
Entrez Id: 23064
Gene Symbol: SETX
SETX 		0.110 Biomarker phenotype HPO