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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00827STEAP2colonMESH:D000756Anemia, Sideroblasticbone marrow
HM00827STEAP2colonMESH:D006332Cardiomegaly
HM00827STEAP2colonMESH:D008103Liver Cirrhosisliver
HM00827STEAP2colonMESH:D009389Neovascularization, Pathologic
HM00827STEAP2colonMESH:D004487Edema
HM00827STEAP2colonMESH:D005885Gingival Hyperplasia
HM00827STEAP2colonMESH:D011528Protozoan Infections
HM00827STEAP2colonMESH:D009436Neural Tube Defects
HM00827STEAP2colonMESH:D017119Porphyria Cutanea Tardaskin
HM00827STEAP2colonMESH:D015428Myocardial Reperfusion Injury
HM00827STEAP2colonMESH:D006528Carcinoma, Hepatocellularliver
HM00827STEAP2colonMESH:D006527Hepatolenticular Degenerationliver
HM00827STEAP2colonMESH:D009135Muscular Diseasesmuscle
HM00827STEAP2colonMESH:D009369Neoplasmsspleen
HM00827STEAP2colonMESH:D009369Neoplasmsbone marrow
HM00827STEAP2colonMESH:D006525Hepatitis, Viral, Human
HM00827STEAP2colonMESH:D006849Hydrocephalusbrain
HM00827STEAP2colonMESH:D010003Osteoarthritisbone
HM00827STEAP2colonMESH:D013226Status Epilepticusmuscle
HM00827STEAP2colonMESH:D013226Status Epilepticusmuscle
HM00827STEAP2colonMESH:D013226Status Epilepticusmuscle
HM00827STEAP2colonMESH:D009139Musculoskeletal Abnormalities
HM00827STEAP2colonMESH:D009181Mycoses
HM00827STEAP2colonMESH:D014178Translocation, Genetic
HM00827STEAP2colonMESH:D018248Adenoma, Liver Cell
HM00827STEAP2colonMESH:D019465Craniofacial Abnormalities
HM00827STEAP2colonMESH:D006529Hepatomegaly
HM00827STEAP2colonMESH:D014564Urogenital Abnormalities
HM00827STEAP2colonMESH:D010212Papillomabrain
HM00827STEAP2colonMESH:D010212Papillomaliver
HM00827STEAP2colonMESH:D010212Papilloma
HM00827STEAP2colonMESH:D017202Myocardial Ischemiaheart
HM00827STEAP2colonMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM00827STEAP2colonMESH:D007638Keratoconjunctivitis Siccaeye
HM00827STEAP2colonMESH:D003920Diabetes Mellituspancreas
HM00827STEAP2colonMESH:D001008Anxiety Disorders
HM00827STEAP2colonMESH:D005355Fibrosis
HM00827STEAP2colonMESH:D007037Hypothyroidismthyroid
HM00827STEAP2colonMESH:D009765Obesity
HM00827STEAP2colonMESH:D002311Cardiomyopathy, Dilatedheart
HM00827STEAP2colonMESH:D017029Epilepsy, Complex Partialmuscle
HM00827STEAP2colonMESH:D009402Nephrosis, Lipoidkidney
HM00827STEAP2colonMESH:D001424Bacterial Infections
HM00827STEAP2colonMESH:D004831Epilepsies, Myoclonicmuscle
HM00827STEAP2colonMESH:D004827Epilepsymuscle
HM00827STEAP2colonMESH:D006943Hyperglycemia
HM00827STEAP2colonMESH:D009190Myelodysplastic Syndromes
HM00827STEAP2colonMESH:D003876Dermatitis, Atopicskin
HM00827STEAP2colonMESH:D004828Epilepsies, Partialmuscle
HM00827STEAP2colonMESH:D001145Arrhythmias, Cardiac
HM00827STEAP2colonMESH:D019189Iron Metabolism Disorders
HM00827STEAP2colonMESH:D012878Skin Neoplasms
HM00827STEAP2colonMESH:D000014Abnormalities, Drug-Induced
HM00827STEAP2colonMESH:D001932Brain Neoplasmsbrain
HM00827STEAP2colonMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00827STEAP2colonMESH:D011471Prostatic Neoplasmsprostate
HM00827STEAP2colonMESH:D020447Parasomnias
HM00827STEAP2colonMESH:D001321Autistic Disorder
HM00827STEAP2colonMESH:D014605Uveitiseye
HM00827STEAP2colonMESH:D010900Pituitary Diseasespituitary
HM00827STEAP2colonMESH:D000740Anemiabone marrow
HM00827STEAP2colonMESH:D050197Atherosclerosiskidney
HM00827STEAP2colonMESH:D050197Atherosclerosisheart
HM00827STEAP2colonMESH:D050197Atherosclerosisblood vessel
HM00827STEAP2colonMESH:D011565Psoriasisskin
HM00827STEAP2colonMESH:D001943Breast Neoplasmsbreast
HM00827STEAP2colonMESH:D007006Hypogonadismtestis
HM00827STEAP2colonMESH:D008664Metal Metabolism, Inborn Errorsskin
HM00827STEAP2colonMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM00827STEAP2colonMESH:D008664Metal Metabolism, Inborn Errorsliver
HM00827STEAP2colonMESH:D008664Metal Metabolism, Inborn Errorskidney
HM00827STEAP2colonMESH:D000690Amyotrophic Lateral Sclerosisnerve
HM00827STEAP2colonMESH:D002779Cholestasisliver
HM00827STEAP2colonMESH:D006432Hemochromatosis
HM00827STEAP2colonMESH:D008113Liver Neoplasms
HM00827STEAP2colonMESH:D008113Liver Neoplasms
HM00827STEAP2colonMESH:D008175Lung Neoplasmslung
HM00827STEAP2colonMESH:D017563Lung Diseases, Interstitiallung
HM00827STEAP2colonMESH:D011041Poisoning
HM00827STEAP2colonMESH:D012208Rhabdomyosarcomarectum
HM00827STEAP2colonMESH:D012208Rhabdomyosarcomaprostate
HM00827STEAP2colonMESH:D012208Rhabdomyosarcomamuscle
HM00827STEAP2colonMESH:D016135Spinal Dysraphismspinal cord
HM00827STEAP2colonMESH:D003110Colonic Neoplasmscolon
HM00827STEAP2colonMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM00827STEAP2colonMESH:D019310Pseudolymphoma
HM00827STEAP2colonMESH:D001778Blood Coagulation Disordersbone marrow
HM00827STEAP2colonMESH:D011225Pre-Eclampsia
HM00827STEAP2colonMESH:D015658HIV Infections
HM00827STEAP2colonMESH:D020961Lewy Body Diseasebrain
HM00827STEAP2colonMESH:D007859Learning Disorders
HM00827STEAP2colonMESH:D020194Unverricht-Lundborg Syndromemuscle
HM00827STEAP2colonMESH:D003922Diabetes Mellitus, Type 1pancreas
HM00827STEAP2colonMESH:D020528Multiple Sclerosis, Chronic Progressivenerve
HM00827STEAP2colonMESH:D007333Insulin Resistance
HM00827STEAP2colonMESH:D005315Fetal Diseases
HM00827STEAP2colonMESH:D014985Xerophthalmiaeye
HM00827STEAP2colonMESH:D008268Macular Degenerationeye
HM00827STEAP2colonMESH:D012148Restless Legs Syndrome
HM00827STEAP2colonMESH:D056486Drug-Induced Liver Injury
HM00827STEAP2colonMESH:D004832Epilepsy, Absencemuscle
HM00827STEAP2colonMESH:D006457Hemoglobinuria, Paroxysmal
HM00827STEAP2colonMESH:D006973Hypertensionlung
HM00827STEAP2colonMESH:D006973Hypertensionheart
HM00827STEAP2colonMESH:D006973Hypertensionblood vessel
HM00827STEAP2colonMESH:D007676Kidney Failure, Chronickidney
HM00827STEAP2colonMESH:D000544Alzheimer Diseasenerve
HM00827STEAP2colonMESH:D001260Ataxia Telangiectasia
HM00827STEAP2colonMESH:D055371Acute Lung Injury
HM00827STEAP2colonMESH:D001714Bipolar Disorder
HM00827STEAP2colonMESH:D009202Cardiomyopathies
HM00827STEAP2colonMESH:D005621Friedreich Ataxiaspinal cord
HM00827STEAP2colonMESH:D006486Hemosiderosis
HM00827STEAP2colonMESH:D006333Heart Failureheart
HM00827STEAP2colonMESH:D009404Nephrotic Syndromekidney
HM00827STEAP2colonMESH:D015427Reperfusion Injury
HM00827STEAP2colonMESH:D008881Migraine Disordersbrain
HM00827STEAP2colonMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM00827STEAP2colonMESH:D006521Hepatitis, Chronicliver
HM00827STEAP2colonMESH:D019636Neurodegenerative Diseasesnerve
HM00827STEAP2colonMESH:D019896alpha 1-Antitrypsin Deficiencylung
HM00827STEAP2colonMESH:D012559Schizophrenia
HM00827STEAP2colonMESH:D007706Menkes Kinky Hair Syndromeskin
HM00827STEAP2colonMESH:D000015Abnormalities, Multiple
HM00827STEAP2colonMESH:D018798Anemia, Iron-Deficiencybone marrow
HM00827STEAP2colonMESH:D012640Seizuresmuscle
HM00827STEAP2colonMESH:D001848Bone Diseases, Developmental
HM00827STEAP2colonMESH:D005234Fatty Liver
HM00827STEAP2colonMESH:D009203Myocardial Infarctionheart
HM00827STEAP2colonMESH:D010024Osteoporosisbone
HM00827STEAP2colonMESH:D013398Sudden Infant Death
HM00827STEAP2colonMESH:D014376Tuberculosis
HM00827STEAP2colonMESH:D000550Amblyopiabrain
HM00827STEAP2colonMESH:D000550Amblyopiabrain
HM00827STEAP2colonMESH:D008108Liver Diseases, Alcoholic
HM00827STEAP2colonMESH:D004421Dystonia
HM00827STEAP2colonMESH:D005317Fetal Growth Retardation
HM00827STEAP2colonMESH:D007674Kidney Diseasesureter
HM00827STEAP2colonMESH:D007674Kidney Diseasespituitary
HM00827STEAP2colonMESH:D007674Kidney Diseaseskidney
HM00827STEAP2colonMESH:D008106Liver Cirrhosis, Experimental
HM00827STEAP2colonMESH:D010300Parkinson Diseasenerve