Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Dysfunctions of the epididymis as a result of primary carnitine deficiency in juvenile visceral steatosis mice. 10100867

1999
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Altered expression of atrial natriuretic peptide and contractile protein genes in hypertrophied ventricle of JVS mice with systemic carnitine deficiency. 9140816

1997
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system. 8155735

1994
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Cardiac hypertrophy in juvenile visceral steatosis (jvs) mice with systemic carnitine deficiency. 8325377

1993
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Animal model of systemic carnitine deficiency: analysis in C3H-H-2 degrees strain of mouse associated with juvenile visceral steatosis. 1996978

1991
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		1.000 Biomarker MGD Infantile disease with microvesicular fatty infiltration of viscera spontaneously occurring in the C3H-H-2(0) strain of mouse with similarities to Reye's syndrome. 3352223

1988