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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00415SPATA17blood vesselMESH:D002341Carotid Artery Thrombosisblood vessel
HM00415SPATA17blood vesselMESH:D013610Tachycardia
HM00415SPATA17blood vesselMESH:D007638Keratoconjunctivitis Siccaeye
HM00415SPATA17blood vesselMESH:D008171Lung Diseases
HM00415SPATA17blood vesselMESH:D013971Thyrotoxicosisthyroid
HM00415SPATA17blood vesselMESH:D010146Pain
HM00415SPATA17blood vesselMESH:D005885Gingival Hyperplasia
HM00415SPATA17blood vesselMESH:D008064Lipidoses
HM00415SPATA17blood vesselMESH:D002386Cataractpancreas
HM00415SPATA17blood vesselMESH:D002386Cataracteye
HM00415SPATA17blood vesselMESH:D001281Atrial Fibrillation
HM00415SPATA17blood vesselMESH:D001145Arrhythmias, Cardiac
HM00415SPATA17blood vesselMESH:D001778Blood Coagulation Disordersbone marrow
HM00415SPATA17blood vesselMESH:D014985Xerophthalmiaeye
HM00415SPATA17blood vesselMESH:D014605Uveitiseye
HM00415SPATA17blood vesselMESH:D008133Long QT Syndrome
HM00415SPATA17blood vesselMESH:D056486Drug-Induced Liver Injury
HM00415SPATA17blood vesselMESH:D008107Liver Diseasesskin
HM00415SPATA17blood vesselMESH:D008107Liver Diseasesmuscle
HM00415SPATA17blood vesselMESH:D008107Liver Diseaseslung
HM00415SPATA17blood vesselMESH:D008107Liver Diseasesliver
HM00415SPATA17blood vesselMESH:D017114Liver Failure, Acute
HM00415SPATA17blood vesselMESH:D008546Melanoma, Experimental
HM00415SPATA17blood vesselMESH:D006930Hyperalgesia
HM00415SPATA17blood vesselMESH:D006973Hypertensionlung
HM00415SPATA17blood vesselMESH:D006973Hypertensionheart
HM00415SPATA17blood vesselMESH:D006973Hypertensionblood vessel
HM00415SPATA17blood vesselMESH:D000799Angioedemaskin
HM00415SPATA17blood vesselMESH:D016171Torsades de Pointes
HM00415SPATA17blood vesselMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM00415SPATA17blood vesselMESH:D006937Hypercholesterolemia
HM00415SPATA17blood vesselMESH:D002311Cardiomyopathy, Dilatedheart
HM00415SPATA17blood vesselMESH:D005234Fatty Liver
HM00415SPATA17blood vesselMESH:D006457Hemoglobinuria, Paroxysmal
HM00415SPATA17blood vesselMESH:D019636Neurodegenerative Diseasesnerve
HM00415SPATA17blood vesselMESH:D011658Pulmonary Fibrosislung
HM00415SPATA17blood vesselMESH:D009181Mycoses
HM00415SPATA17blood vesselMESH:D009402Nephrosis, Lipoidkidney
HM00415SPATA17blood vesselMESH:D005355Fibrosis
HM00415SPATA17blood vesselMESH:D009404Nephrotic Syndromekidney
HM00415SPATA17blood vesselMESH:D007037Hypothyroidismthyroid
HM00415SPATA17blood vesselMESH:D013959Thyroid Diseasesthyroid
HM00415SPATA17blood vesselMESH:D011565Psoriasisskin
HM00415SPATA17blood vesselMESH:D014581Urticariaskin
HM00415SPATA17blood vesselMESH:D006529Hepatomegaly
HM00415SPATA17blood vesselMESH:D007674Kidney Diseasesureter
HM00415SPATA17blood vesselMESH:D007674Kidney Diseasespituitary
HM00415SPATA17blood vesselMESH:D007674Kidney Diseaseskidney
HM00415SPATA17blood vesselMESH:D008664Metal Metabolism, Inborn Errorsskin
HM00415SPATA17blood vesselMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM00415SPATA17blood vesselMESH:D008664Metal Metabolism, Inborn Errorsliver
HM00415SPATA17blood vesselMESH:D008664Metal Metabolism, Inborn Errorskidney
HM00415SPATA17blood vesselMESH:D001321Autistic Disorder
HM00415SPATA17blood vesselMESH:D013276Stomach Ulcer
HM00415SPATA17blood vesselOMIM:609620SHORT QT SYNDROME 1
HM00415SPATA17blood vesselMESH:D017563Lung Diseases, Interstitiallung
HM00415SPATA17blood vesselMESH:D017180Tachycardia, Ventricular