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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01657STK40stomachMESH:D012878Skin Neoplasms
HM01657STK40stomachMESH:D017114Liver Failure, Acute
HM01657STK40stomachMESH:D001943Breast Neoplasmsbreast
HM01657STK40stomachMESH:D015428Myocardial Reperfusion Injury
HM01657STK40stomachMESH:D002386Cataractpancreas
HM01657STK40stomachMESH:D002386Cataracteye
HM01657STK40stomachMESH:D001161Arteriosclerosisblood vessel
HM01657STK40stomachMESH:D006333Heart Failureheart
HM01657STK40stomachMESH:D015619Respiratory System Abnormalities
HM01657STK40stomachMESH:D009135Muscular Diseasesmuscle
HM01657STK40stomachMESH:D005885Gingival Hyperplasia
HM01657STK40stomachMESH:D006943Hyperglycemia
HM01657STK40stomachMESH:D008175Lung Neoplasmslung
HM01657STK40stomachMESH:D001321Autistic Disorder
HM01657STK40stomachMESH:D008106Liver Cirrhosis, Experimental
HM01657STK40stomachMESH:D014581Urticariaskin
HM01657STK40stomachMESH:D009369Neoplasmsspleen
HM01657STK40stomachMESH:D009369Neoplasmsbone marrow
HM01657STK40stomachMESH:D006470Hemorrhage
HM01657STK40stomachMESH:D009765Obesity
HM01657STK40stomachMESH:D004487Edema
HM01657STK40stomachMESH:D005355Fibrosis
HM01657STK40stomachMESH:D015427Reperfusion Injury
HM01657STK40stomachMESH:D005124Eye Abnormalities
HM01657STK40stomachMESH:D009404Nephrotic Syndromekidney
HM01657STK40stomachMESH:D017119Porphyria Cutanea Tardaskin
HM01657STK40stomachMESH:D019636Neurodegenerative Diseasesnerve
HM01657STK40stomachMESH:D018248Adenoma, Liver Cell
HM01657STK40stomachMESH:D007638Keratoconjunctivitis Siccaeye
HM01657STK40stomachMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01657STK40stomachMESH:D009421Nervous System Malformations
HM01657STK40stomachMESH:D002972Cleft Palate
HM01657STK40stomachMESH:D008107Liver Diseasesskin
HM01657STK40stomachMESH:D008107Liver Diseasesmuscle
HM01657STK40stomachMESH:D008107Liver Diseaseslung
HM01657STK40stomachMESH:D008107Liver Diseasesliver
HM01657STK40stomachMESH:D011297Prenatal Exposure Delayed Effects
HM01657STK40stomachMESH:D000014Abnormalities, Drug-Induced
HM01657STK40stomachMESH:D006332Cardiomegaly
HM01657STK40stomachMESH:D005313Fetal Death
HM01657STK40stomachMESH:D054079Vascular Malformations
HM01657STK40stomachMESH:D000740Anemiabone marrow
HM01657STK40stomachMESH:D055371Acute Lung Injury
HM01657STK40stomachMESH:D000013Congenital Abnormalities
HM01657STK40stomachMESH:D007674Kidney Diseasesureter
HM01657STK40stomachMESH:D007674Kidney Diseasespituitary
HM01657STK40stomachMESH:D007674Kidney Diseaseskidney
HM01657STK40stomachMESH:D007333Insulin Resistance
HM01657STK40stomachMESH:D003876Dermatitis, Atopicskin
HM01657STK40stomachMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01657STK40stomachMESH:D010382Peliosis Hepatisliver
HM01657STK40stomachMESH:D006457Hemoglobinuria, Paroxysmal
HM01657STK40stomachMESH:D010146Pain
HM01657STK40stomachMESH:D006330Heart Defects, Congenital
HM01657STK40stomachMESH:D009402Nephrosis, Lipoidkidney
HM01657STK40stomachMESH:D014985Xerophthalmiaeye
HM01657STK40stomachMESH:D001778Blood Coagulation Disordersbone marrow
HM01657STK40stomachMESH:D004489Edema, Cardiac
HM01657STK40stomachMESH:D008103Liver Cirrhosisliver
HM01657STK40stomachMESH:D014605Uveitiseye
HM01657STK40stomachMESH:D001836Body Weight Changes
HM01657STK40stomachMESH:D013959Thyroid Diseasesthyroid
HM01657STK40stomachMESH:D000799Angioedemaskin
HM01657STK40stomachMESH:D005234Fatty Liver
HM01657STK40stomachMESH:D007569Jaw Abnormalities
HM01657STK40stomachMESH:D011565Psoriasisskin
HM01657STK40stomachMESH:D004362Drug Toxicity
HM01657STK40stomachMESH:D008113Liver Neoplasms
HM01657STK40stomachMESH:D008113Liver Neoplasms
HM01657STK40stomachMESH:D019465Craniofacial Abnormalities
HM01657STK40stomachMESH:D006529Hepatomegaly
HM01657STK40stomachMESH:D006869Hydronephrosiskidney
HM01657STK40stomachMESH:D006973Hypertensionlung
HM01657STK40stomachMESH:D006973Hypertensionheart
HM01657STK40stomachMESH:D006973Hypertensionblood vessel
HM01657STK40stomachMESH:D009203Myocardial Infarctionheart
HM01657STK40stomachMESH:D056486Drug-Induced Liver Injury
HM01657STK40stomachMESH:D002277Carcinoma
HM01657STK40stomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01657STK40stomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01657STK40stomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01657STK40stomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01657STK40stomachMESH:D017202Myocardial Ischemiaheart
HM01657STK40stomachMESH:D018281Cholangiocarcinomaliver
HM01657STK40stomachMESH:D019282Wasting Syndrome
HM01657STK40stomachMESH:D050171Dyslipidemias
HM01657STK40stomachMESH:D007249Inflammation
HM01657STK40stomachMESH:D006930Hyperalgesia
HM01657STK40stomachMESH:D002779Cholestasisliver
HM01657STK40stomachMESH:D008546Melanoma, Experimental
HM01657STK40stomachMESH:D008114Liver Neoplasms, Experimental
HM01657STK40stomachMESH:D001848Bone Diseases, Developmental