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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01023GMPRstomachMESH:D004489Edema, Cardiac
HM01023GMPRstomachMESH:D009190Myelodysplastic Syndromes
HM01023GMPRstomachMESH:D005234Fatty Liver
HM01023GMPRstomachMESH:D008106Liver Cirrhosis, Experimental
HM01023GMPRstomachMESH:D008881Migraine Disordersbrain
HM01023GMPRstomachMESH:D012559Schizophrenia
HM01023GMPRstomachMESH:D016135Spinal Dysraphismspinal cord
HM01023GMPRstomachMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01023GMPRstomachMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01023GMPRstomachMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01023GMPRstomachMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01023GMPRstomachMESH:D006470Hemorrhage
HM01023GMPRstomachMESH:D002972Cleft Palate
HM01023GMPRstomachMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01023GMPRstomachMESH:D008114Liver Neoplasms, Experimental
HM01023GMPRstomachMESH:D011297Prenatal Exposure Delayed Effects
HM01023GMPRstomachMESH:D014594Uterine Neoplasmscervix
HM01023GMPRstomachMESH:D014594Uterine Neoplasms
HM01023GMPRstomachMESH:D002252Carbon Tetrachloride Poisoning
HM01023GMPRstomachMESH:D004362Drug Toxicity
HM01023GMPRstomachMESH:D005355Fibrosis
HM01023GMPRstomachMESH:D004832Epilepsy, Absencemuscle
HM01023GMPRstomachMESH:D013226Status Epilepticusmuscle
HM01023GMPRstomachMESH:D013226Status Epilepticusmuscle
HM01023GMPRstomachMESH:D013226Status Epilepticusmuscle
HM01023GMPRstomachMESH:D018281Cholangiocarcinomaliver
HM01023GMPRstomachMESH:D004827Epilepsymuscle
HM01023GMPRstomachMESH:D014605Uveitiseye
HM01023GMPRstomachMESH:D009421Nervous System Malformations
HM01023GMPRstomachMESH:D013927Thrombosis
HM01023GMPRstomachMESH:D011565Psoriasisskin
HM01023GMPRstomachMESH:D054079Vascular Malformations
HM01023GMPRstomachMESH:D006457Hemoglobinuria, Paroxysmal
HM01023GMPRstomachMESH:D001714Bipolar Disorder
HM01023GMPRstomachMESH:D017119Porphyria Cutanea Tardaskin
HM01023GMPRstomachMESH:D005124Eye Abnormalities
HM01023GMPRstomachMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM01023GMPRstomachMESH:D009069Movement Disordersnerve
HM01023GMPRstomachMESH:D009069Movement Disordersbrain
HM01023GMPRstomachMESH:D017202Myocardial Ischemiaheart
HM01023GMPRstomachMESH:D009402Nephrosis, Lipoidkidney
HM01023GMPRstomachMESH:D001848Bone Diseases, Developmental
HM01023GMPRstomachMESH:D009436Neural Tube Defects
HM01023GMPRstomachMESH:D005885Gingival Hyperplasia
HM01023GMPRstomachMESH:D008569Memory Disorders
HM01023GMPRstomachMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01023GMPRstomachMESH:D018248Adenoma, Liver Cell
HM01023GMPRstomachMESH:D017563Lung Diseases, Interstitiallung
HM01023GMPRstomachMESH:D012878Skin Neoplasms
HM01023GMPRstomachMESH:D006932Hyperbilirubinemia
HM01023GMPRstomachMESH:D000152Acne Vulgaris
HM01023GMPRstomachMESH:D004831Epilepsies, Myoclonicmuscle
HM01023GMPRstomachMESH:D008113Liver Neoplasms
HM01023GMPRstomachMESH:D008113Liver Neoplasms
HM01023GMPRstomachMESH:D007674Kidney Diseasesureter
HM01023GMPRstomachMESH:D007674Kidney Diseasespituitary
HM01023GMPRstomachMESH:D007674Kidney Diseaseskidney
HM01023GMPRstomachMESH:D004828Epilepsies, Partialmuscle
HM01023GMPRstomachMESH:D005317Fetal Growth Retardation
HM01023GMPRstomachMESH:D019282Wasting Syndrome
HM01023GMPRstomachMESH:D001008Anxiety Disorders
HM01023GMPRstomachMESH:D012640Seizuresmuscle
HM01023GMPRstomachMESH:D002471Cell Transformation, Neoplastic
HM01023GMPRstomachMESH:D006849Hydrocephalusbrain
HM01023GMPRstomachMESH:D007638Keratoconjunctivitis Siccaeye
HM01023GMPRstomachMESH:D000015Abnormalities, Multiple
HM01023GMPRstomachMESH:D004487Edema
HM01023GMPRstomachMESH:D000013Congenital Abnormalities
HM01023GMPRstomachMESH:D019851Thrombophiliabone marrow
HM01023GMPRstomachMESH:D003704Dementianerve
HM01023GMPRstomachMESH:D003704Dementiablood vessel
HM01023GMPRstomachMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01023GMPRstomachMESH:D005315Fetal Diseases
HM01023GMPRstomachMESH:D009139Musculoskeletal Abnormalities
HM01023GMPRstomachMESH:D015619Respiratory System Abnormalities
HM01023GMPRstomachMESH:D005313Fetal Death
HM01023GMPRstomachMESH:D019310Pseudolymphoma
HM01023GMPRstomachMESH:D006332Cardiomegaly
HM01023GMPRstomachMESH:D006505Hepatitis
HM01023GMPRstomachMESH:D011537Pruritus
HM01023GMPRstomachMESH:D001161Arteriosclerosisblood vessel
HM01023GMPRstomachMESH:D019465Craniofacial Abnormalities
HM01023GMPRstomachMESH:D009404Nephrotic Syndromekidney
HM01023GMPRstomachMESH:D001778Blood Coagulation Disordersbone marrow
HM01023GMPRstomachMESH:D006330Heart Defects, Congenital
HM01023GMPRstomachMESH:D007569Jaw Abnormalities
HM01023GMPRstomachMESH:D001169Arthritis, Experimental
HM01023GMPRstomachMESH:D001943Breast Neoplasmsbreast
HM01023GMPRstomachMESH:D008107Liver Diseasesskin
HM01023GMPRstomachMESH:D008107Liver Diseasesmuscle
HM01023GMPRstomachMESH:D008107Liver Diseaseslung
HM01023GMPRstomachMESH:D008107Liver Diseasesliver
HM01023GMPRstomachMESH:D020246Venous Thrombosis
HM01023GMPRstomachMESH:D000014Abnormalities, Drug-Induced
HM01023GMPRstomachMESH:D006973Hypertensionlung
HM01023GMPRstomachMESH:D006973Hypertensionheart
HM01023GMPRstomachMESH:D006973Hypertensionblood vessel
HM01023GMPRstomachMESH:D007248Infertility, Male
HM01023GMPRstomachMESH:D006529Hepatomegaly
HM01023GMPRstomachMESH:D008103Liver Cirrhosisliver
HM01023GMPRstomachMESH:D056486Drug-Induced Liver Injury
HM01023GMPRstomachMESH:D004421Dystonia
HM01023GMPRstomachMESH:D017029Epilepsy, Complex Partialmuscle
HM01023GMPRstomachMESH:D013959Thyroid Diseasesthyroid
HM01023GMPRstomachMESH:D001836Body Weight Changes
HM01023GMPRstomachMESH:D007247Infertility, Female
HM01023GMPRstomachMESH:D017114Liver Failure, Acute
HM01023GMPRstomachMESH:D006869Hydronephrosiskidney
HM01023GMPRstomachMESH:D007249Inflammation
HM01023GMPRstomachMESH:D017093Liver Failure
HM01023GMPRstomachMESH:D002779Cholestasisliver
HM01023GMPRstomachMESH:D001321Autistic Disorder
HM01023GMPRstomachMESH:D002277Carcinoma
HM01023GMPRstomachMESH:D013088Spermatocele
HM01023GMPRstomachMESH:D000740Anemiabone marrow
HM01023GMPRstomachMESH:D016584Panic Disorder
HM01023GMPRstomachMESH:D000230Adenocarcinoma
HM01023GMPRstomachMESH:D000230Adenocarcinomauterus
HM01023GMPRstomachMESH:D000230Adenocarcinoma
HM01023GMPRstomachMESH:D000230Adenocarcinoma
HM01023GMPRstomachMESH:D000230Adenocarcinomauterus
HM01023GMPRstomachMESH:D000230Adenocarcinomathyroid
HM01023GMPRstomachMESH:D000230Adenocarcinomaskin
HM01023GMPRstomachMESH:D000230Adenocarcinomaparathyroid gland
HM01023GMPRstomachMESH:D000230Adenocarcinomaliver
HM01023GMPRstomachMESH:D000230Adenocarcinomakidney
HM01023GMPRstomachMESH:D000230Adenocarcinomaeye
HM01023GMPRstomachMESH:D000230Adenocarcinomaadrenal gland
HM01023GMPRstomachMESH:D007021Hypospadias
HM01023GMPRstomachMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01023GMPRstomachMESH:D008175Lung Neoplasmslung
HM01023GMPRstomachMESH:D014178Translocation, Genetic
HM01023GMPRstomachMESH:D012208Rhabdomyosarcomarectum
HM01023GMPRstomachMESH:D012208Rhabdomyosarcomaprostate
HM01023GMPRstomachMESH:D012208Rhabdomyosarcomamuscle
HM01023GMPRstomachMESH:D014985Xerophthalmiaeye
HM01023GMPRstomachMESH:D010382Peliosis Hepatisliver
HM01023GMPRstomachMESH:D000550Amblyopiabrain
HM01023GMPRstomachMESH:D000550Amblyopiabrain
HM01023GMPRstomachMESH:D014564Urogenital Abnormalities