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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05636EPM2AIP1larynxMESH:D001749Urinary Bladder Neoplasmsureter
HM05636EPM2AIP1larynxMESH:D001749Urinary Bladder Neoplasmsbladder
HM05636EPM2AIP1larynxMESH:D008546Melanoma, Experimental
HM05636EPM2AIP1larynxMESH:D011297Prenatal Exposure Delayed Effects
HM05636EPM2AIP1larynxMESH:D014652Vascular Diseasesspinal cord
HM05636EPM2AIP1larynxMESH:D014652Vascular Diseaseslung
HM05636EPM2AIP1larynxMESH:D014652Vascular Diseasesliver
HM05636EPM2AIP1larynxMESH:D014652Vascular Diseaseskidney
HM05636EPM2AIP1larynxMESH:D014652Vascular Diseasesblood vessel
HM05636EPM2AIP1larynxMESH:D003924Diabetes Mellitus, Type 2pancreas
HM05636EPM2AIP1larynxMESH:D002318Cardiovascular Diseasesheart
HM05636EPM2AIP1larynxMESH:D002318Cardiovascular Diseasesbone marrow
HM05636EPM2AIP1larynxMESH:D002318Cardiovascular Diseasesblood vessel
HM05636EPM2AIP1larynxMESH:D004489Edema, Cardiac
HM05636EPM2AIP1larynxMESH:D019046Bone Marrow Neoplasms
HM05636EPM2AIP1larynxMESH:D002252Carbon Tetrachloride Poisoning
HM05636EPM2AIP1larynxMESH:D008107Liver Diseasesskin
HM05636EPM2AIP1larynxMESH:D008107Liver Diseasesmuscle
HM05636EPM2AIP1larynxMESH:D008107Liver Diseaseslung
HM05636EPM2AIP1larynxMESH:D008107Liver Diseasesliver
HM05636EPM2AIP1larynxMESH:D000014Abnormalities, Drug-Induced
HM05636EPM2AIP1larynxMESH:D000740Anemiabone marrow
HM05636EPM2AIP1larynxMESH:D000799Angioedemaskin
HM05636EPM2AIP1larynxMESH:D017488Hyperkeratosis, Epidermolytic
HM05636EPM2AIP1larynxMESH:D007569Jaw Abnormalities
HM05636EPM2AIP1larynxMESH:D004362Drug Toxicity
HM05636EPM2AIP1larynxMESH:D012512Sarcoma, Ewing's
HM05636EPM2AIP1larynxMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM05636EPM2AIP1larynxMESH:D050197Atherosclerosiskidney
HM05636EPM2AIP1larynxMESH:D050197Atherosclerosisheart
HM05636EPM2AIP1larynxMESH:D050197Atherosclerosisblood vessel
HM05636EPM2AIP1larynxMESH:D002294Carcinoma, Squamous Celllung
HM05636EPM2AIP1larynxMESH:D002294Carcinoma, Squamous Cellliver
HM05636EPM2AIP1larynxMESH:D002294Carcinoma, Squamous Celllarynx
HM05636EPM2AIP1larynxMESH:D002294Carcinoma, Squamous Cellkidney
HM05636EPM2AIP1larynxMESH:D002294Carcinoma, Squamous Celleye
HM05636EPM2AIP1larynxMESH:D008113Liver Neoplasms
HM05636EPM2AIP1larynxMESH:D008113Liver Neoplasms
HM05636EPM2AIP1larynxMESH:D018281Cholangiocarcinomaliver
HM05636EPM2AIP1larynxMESH:D005234Fatty Liver
HM05636EPM2AIP1larynxMESH:D007674Kidney Diseasesureter
HM05636EPM2AIP1larynxMESH:D007674Kidney Diseasespituitary
HM05636EPM2AIP1larynxMESH:D007674Kidney Diseaseskidney
HM05636EPM2AIP1larynxMESH:D008106Liver Cirrhosis, Experimental
HM05636EPM2AIP1larynxMESH:D010146Pain
HM05636EPM2AIP1larynxMESH:D054079Vascular Malformations
HM05636EPM2AIP1larynxMESH:D006930Hyperalgesia
HM05636EPM2AIP1larynxMESH:D017119Porphyria Cutanea Tardaskin
HM05636EPM2AIP1larynxMESH:D012878Skin Neoplasms
HM05636EPM2AIP1larynxMESH:D001321Autistic Disorder
HM05636EPM2AIP1larynxMESH:D014581Urticariaskin
HM05636EPM2AIP1larynxMESH:D006973Hypertensionlung
HM05636EPM2AIP1larynxMESH:D006973Hypertensionheart
HM05636EPM2AIP1larynxMESH:D006973Hypertensionblood vessel
HM05636EPM2AIP1larynxMESH:D007642Keratosisskin
HM05636EPM2AIP1larynxMESH:D017114Liver Failure, Acute
HM05636EPM2AIP1larynxMESH:D056486Drug-Induced Liver Injury
HM05636EPM2AIP1larynxMESH:D017093Liver Failure
HM05636EPM2AIP1larynxMESH:D013959Thyroid Diseasesthyroid
HM05636EPM2AIP1larynxMESH:D006932Hyperbilirubinemia
HM05636EPM2AIP1larynxMESH:D010190Pancreatic Neoplasmspancreas
HM05636EPM2AIP1larynxMESH:D006332Cardiomegaly
HM05636EPM2AIP1larynxMESH:D018246Adrenocortical Adenoma
HM05636EPM2AIP1larynxMESH:D004487Edema
HM05636EPM2AIP1larynxMESH:D006470Hemorrhage
HM05636EPM2AIP1larynxMESH:D008114Liver Neoplasms, Experimental
HM05636EPM2AIP1larynxMESH:D016491Peripheral Vascular Diseases
HM05636EPM2AIP1larynxMESH:D019465Craniofacial Abnormalities
HM05636EPM2AIP1larynxMESH:D017202Myocardial Ischemiaheart
HM05636EPM2AIP1larynxMESH:D015619Respiratory System Abnormalities
HM05636EPM2AIP1larynxMESH:D005534Foot Diseases
HM05636EPM2AIP1larynxMESH:D024801Tauopathiesnerve
HM05636EPM2AIP1larynxMESH:D006330Heart Defects, Congenital
HM05636EPM2AIP1larynxMESH:D005313Fetal Death
HM05636EPM2AIP1larynxMESH:D006505Hepatitis
HM05636EPM2AIP1larynxMESH:D002280Carcinoma, Basal Cell
HM05636EPM2AIP1larynxMESH:D006529Hepatomegaly
HM05636EPM2AIP1larynxMESH:D006689Hodgkin Disease
HM05636EPM2AIP1larynxMESH:D010382Peliosis Hepatisliver
HM05636EPM2AIP1larynxMESH:D002386Cataractpancreas
HM05636EPM2AIP1larynxMESH:D002386Cataracteye
HM05636EPM2AIP1larynxMESH:D001836Body Weight Changes
HM05636EPM2AIP1larynxMESH:D001778Blood Coagulation Disordersbone marrow
HM05636EPM2AIP1larynxMESH:D002340Carotid Artery Diseasesblood vessel
HM05636EPM2AIP1larynxMESH:D005355Fibrosis
HM05636EPM2AIP1larynxMESH:D006561Herpes Simplex
HM05636EPM2AIP1larynxMESH:D008103Liver Cirrhosisliver
HM05636EPM2AIP1larynxMESH:D020078Neurogenic Inflammation
HM05636EPM2AIP1larynxMESH:D000013Congenital Abnormalities
HM05636EPM2AIP1larynxMESH:D001943Breast Neoplasmsbreast
HM05636EPM2AIP1larynxMESH:D002295Carcinoma, Transitional Cell
HM05636EPM2AIP1larynxMESH:D001848Bone Diseases, Developmental
HM05636EPM2AIP1larynxMESH:D015473Leukemia, Promyelocytic, Acute
HM05636EPM2AIP1larynxMESH:D008223Lymphoma
HM05636EPM2AIP1larynxMESH:D006869Hydronephrosiskidney
HM05636EPM2AIP1larynxMESH:D007249Inflammation
HM05636EPM2AIP1larynxMESH:D008175Lung Neoplasmslung
HM05636EPM2AIP1larynxMESH:D011471Prostatic Neoplasmsprostate
HM05636EPM2AIP1larynxMESH:D018248Adenoma, Liver Cell
HM05636EPM2AIP1larynxMESH:D009436Neural Tube Defects
HM05636EPM2AIP1larynxMESH:D012871Skin Diseasesskin
HM05636EPM2AIP1larynxMESH:D002972Cleft Palate
HM05636EPM2AIP1larynxMESH:D006528Carcinoma, Hepatocellularliver
HM05636EPM2AIP1larynxMESH:D010051Ovarian Neoplasmsuterus
HM05636EPM2AIP1larynxMESH:D010051Ovarian Neoplasms
HM05636EPM2AIP1larynxMESH:D054198Precursor Cell Lymphoblastic Leukemia-Lymphoma
HM05636EPM2AIP1larynxMESH:D002277Carcinoma
HM05636EPM2AIP1larynxMESH:D009421Nervous System Malformations
HM05636EPM2AIP1larynxMESH:D020261Arsenic Poisoning
HM05636EPM2AIP1larynxMESH:D005124Eye Abnormalities
HM05636EPM2AIP1larynxMESH:D019282Wasting Syndrome
HM05636EPM2AIP1larynxMESH:D019636Neurodegenerative Diseasesnerve