Source: RGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
Diabetes Mellitus, Non-Insulin-Dependent
disease 0.300 None 0.931 1 0 1998 2020
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0018801
Disease: Heart failure
Heart failure
disease 0.220 None 1.000 1 0 2002 2018
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease 0.220 None 1.000 1 0 2002 2018
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
disease 0.210 None 1.000 1 0 2005 2007
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group 0.210 None 1.000 1 0 2000 2018
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0362046
Disease: Prediabetes syndrome
Prediabetes syndrome
disease 0.210 None 1.000 1 0 2003 2018
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease 0.210 None 1.000 1 0 2007 2007
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy
disease 0.200 None 1.000 1 0 2007 2007
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0027055
Disease: Myocardial Reperfusion Injury
Myocardial Reperfusion Injury
phenotype 0.200 None 1.000 1 0 2009 2009
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
disease 0.200 None 1.000 1 0 2000 2000
Entrez Id: 7352
Gene Symbol: UCP3
UCP3
uncoupling protein 3 0.619 0.577 9.6E-10
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.200 None 1.000 1 0 2012 2012