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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02785SNTG2blood vesselMESH:D010146Pain
HM02785SNTG2blood vesselMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM02785SNTG2blood vesselMESH:D001321Autistic Disorder
HM02785SNTG2blood vesselMESH:D008546Melanoma, Experimental
HM02785SNTG2blood vesselMESH:D007674Kidney Diseasesureter
HM02785SNTG2blood vesselMESH:D007674Kidney Diseasespituitary
HM02785SNTG2blood vesselMESH:D007674Kidney Diseaseskidney
HM02785SNTG2blood vesselMESH:D056486Drug-Induced Liver Injury
HM02785SNTG2blood vesselMESH:D019636Neurodegenerative Diseasesnerve
HM02785SNTG2blood vesselMESH:D008107Liver Diseasesskin
HM02785SNTG2blood vesselMESH:D008107Liver Diseasesmuscle
HM02785SNTG2blood vesselMESH:D008107Liver Diseaseslung
HM02785SNTG2blood vesselMESH:D008107Liver Diseasesliver
HM02785SNTG2blood vesselMESH:D014581Urticariaskin
HM02785SNTG2blood vesselMESH:D000799Angioedemaskin
HM02785SNTG2blood vesselMESH:D002386Cataractpancreas
HM02785SNTG2blood vesselMESH:D002386Cataracteye
HM02785SNTG2blood vesselMESH:D006930Hyperalgesia
HM02785SNTG2blood vesselMESH:D017114Liver Failure, Acute