Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease BEFREE Our results suggest that the examined region of Epsin 4 does not have a major influence on susceptibility to schizophrenia in Japanese. 18696005 2008
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 Biomarker disease BEFREE This provides additional support for the involvement of enthoprotin in the pathogenesis of schizophrenia and other psychotic disorders. 18929466 2008
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease BEFREE This study thus fails to support an association of genetic variations in the ENTH gene and schizophrenia. 16616458 2006
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease BEFREE Interestingly, this region has been implicated in several previous genetic studies of schizophrenia and psychosis, including disease association with variants of the enthoprotin and gamma-aminobutyric acid receptor genes. 16984960 2006
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease BEFREE Our results indicate the presence of a locus near the 5' end of Epsin 4 conferring susceptibility to the disease and provide further support for Epsin 4 as an important potential contributor to genetic risk in schizophrenia. 16402136 2006
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease LHGDN Our results indicate the presence of a locus near the 5' end of Epsin 4 conferring susceptibility to the disease and provide further support for Epsin 4 as an important potential contributor to genetic risk in schizophrenia. 16402136 2006
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 AlteredExpression disease BEFREE A genetically determined abnormality in the structure, function, or expression of enthoprotin is likely to be responsible for genetic susceptibility to a subtype of schizophrenia on chromosome 5q33.3. 15793701 2005
Entrez Id: 9685
Gene Symbol: CLINT1
CLINT1
0.060 GeneticVariation disease LHGDN A genetically determined abnormality in the structure, function, or expression of enthoprotin is likely to be responsible for genetic susceptibility to a subtype of schizophrenia on chromosome 5q33.3. 15793701 2005