Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00169CELA3BpancreasMESH:D004362Drug Toxicity
HM00169CELA3BpancreasMESH:D009369Neoplasmsspleen
HM00169CELA3BpancreasMESH:D009369Neoplasmsbone marrow
HM00169CELA3BpancreasMESH:D004489Edema, Cardiac
HM00169CELA3BpancreasMESH:D013959Thyroid Diseasesthyroid
HM00169CELA3BpancreasMESH:D015619Respiratory System Abnormalities
HM00169CELA3BpancreasMESH:D002972Cleft Palate
HM00169CELA3BpancreasMESH:D008106Liver Cirrhosis, Experimental
HM00169CELA3BpancreasMESH:D000014Abnormalities, Drug-Induced
HM00169CELA3BpancreasMESH:D005124Eye Abnormalities
HM00169CELA3BpancreasMESH:D008175Lung Neoplasmslung
HM00169CELA3BpancreasMESH:D009765Obesity
HM00169CELA3BpancreasMESH:D017119Porphyria Cutanea Tardaskin
HM00169CELA3BpancreasMESH:D001848Bone Diseases, Developmental
HM00169CELA3BpancreasMESH:D006470Hemorrhage
HM00169CELA3BpancreasMESH:D006332Cardiomegaly
HM00169CELA3BpancreasMESH:D017202Myocardial Ischemiaheart
HM00169CELA3BpancreasMESH:D009421Nervous System Malformations
HM00169CELA3BpancreasMESH:D055371Acute Lung Injury
HM00169CELA3BpancreasMESH:D007249Inflammation
HM00169CELA3BpancreasMESH:D019282Wasting Syndrome
HM00169CELA3BpancreasMESH:D010382Peliosis Hepatisliver
HM00169CELA3BpancreasMESH:D007569Jaw Abnormalities
HM00169CELA3BpancreasMESH:D004487Edema
HM00169CELA3BpancreasMESH:D007333Insulin Resistance
HM00169CELA3BpancreasMESH:D006330Heart Defects, Congenital
HM00169CELA3BpancreasMESH:D000740Anemiabone marrow
HM00169CELA3BpancreasMESH:D001778Blood Coagulation Disordersbone marrow
HM00169CELA3BpancreasMESH:D000013Congenital Abnormalities
HM00169CELA3BpancreasMESH:D001943Breast Neoplasmsbreast
HM00169CELA3BpancreasMESH:D002779Cholestasisliver
HM00169CELA3BpancreasMESH:D009203Myocardial Infarctionheart
HM00169CELA3BpancreasMESH:D005355Fibrosis
HM00169CELA3BpancreasMESH:D056486Drug-Induced Liver Injury
HM00169CELA3BpancreasMESH:D009135Muscular Diseasesmuscle
HM00169CELA3BpancreasMESH:D050197Atherosclerosiskidney
HM00169CELA3BpancreasMESH:D050197Atherosclerosisheart
HM00169CELA3BpancreasMESH:D050197Atherosclerosisblood vessel
HM00169CELA3BpancreasMESH:D003876Dermatitis, Atopicskin
HM00169CELA3BpancreasMESH:D006973Hypertensionlung
HM00169CELA3BpancreasMESH:D006973Hypertensionheart
HM00169CELA3BpancreasMESH:D006973Hypertensionblood vessel
HM00169CELA3BpancreasMESH:D005234Fatty Liver
HM00169CELA3BpancreasMESH:D018281Cholangiocarcinomaliver
HM00169CELA3BpancreasMESH:D001836Body Weight Changes
HM00169CELA3BpancreasMESH:D006333Heart Failureheart
HM00169CELA3BpancreasMESH:D008113Liver Neoplasms
HM00169CELA3BpancreasMESH:D008113Liver Neoplasms
HM00169CELA3BpancreasMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00169CELA3BpancreasMESH:D015428Myocardial Reperfusion Injury
HM00169CELA3BpancreasMESH:D012878Skin Neoplasms
HM00169CELA3BpancreasMESH:D006529Hepatomegaly
HM00169CELA3BpancreasMESH:D019465Craniofacial Abnormalities
HM00169CELA3BpancreasMESH:D054079Vascular Malformations
HM00169CELA3BpancreasMESH:D008114Liver Neoplasms, Experimental
HM00169CELA3BpancreasMESH:D018248Adenoma, Liver Cell
HM00169CELA3BpancreasMESH:D002318Cardiovascular Diseasesheart
HM00169CELA3BpancreasMESH:D002318Cardiovascular Diseasesbone marrow
HM00169CELA3BpancreasMESH:D002318Cardiovascular Diseasesblood vessel
HM00169CELA3BpancreasMESH:D013276Stomach Ulcer
HM00169CELA3BpancreasMESH:D002277Carcinoma
HM00169CELA3BpancreasMESH:D005313Fetal Death
HM00169CELA3BpancreasMESH:D011297Prenatal Exposure Delayed Effects
HM00169CELA3BpancreasMESH:D006869Hydronephrosiskidney
HM00169CELA3BpancreasMESH:D015427Reperfusion Injury
HM00169CELA3BpancreasMESH:D006943Hyperglycemia