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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04269URB1stomachMESH:D002386Cataractpancreas
HM04269URB1stomachMESH:D002386Cataracteye
HM04269URB1stomachMESH:D010146Pain
HM04269URB1stomachMESH:D017114Liver Failure, Acute
HM04269URB1stomachMESH:D007249Inflammation
HM04269URB1stomachMESH:D001289Attention Deficit Disorder with Hyperactivity
HM04269URB1stomachMESH:D014581Urticariaskin
HM04269URB1stomachMESH:D000799Angioedemaskin
HM04269URB1stomachMESH:D008546Melanoma, Experimental
HM04269URB1stomachMESH:D056486Drug-Induced Liver Injury
HM04269URB1stomachMESH:D008107Liver Diseasesskin
HM04269URB1stomachMESH:D008107Liver Diseasesmuscle
HM04269URB1stomachMESH:D008107Liver Diseaseslung
HM04269URB1stomachMESH:D008107Liver Diseasesliver
HM04269URB1stomachMESH:D007674Kidney Diseasesureter
HM04269URB1stomachMESH:D007674Kidney Diseasespituitary
HM04269URB1stomachMESH:D007674Kidney Diseaseskidney
HM04269URB1stomachMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM04269URB1stomachMESH:D019636Neurodegenerative Diseasesnerve
HM04269URB1stomachMESH:D006930Hyperalgesia
HM04269URB1stomachMESH:D001321Autistic Disorder