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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01822SCPEP1esophagusMESH:D004489Edema, Cardiac
HM01822SCPEP1esophagusMESH:D015473Leukemia, Promyelocytic, Acute
HM01822SCPEP1esophagusMESH:D001836Body Weight Changes
HM01822SCPEP1esophagusMESH:D002295Carcinoma, Transitional Cell
HM01822SCPEP1esophagusMESH:D001749Urinary Bladder Neoplasmsureter
HM01822SCPEP1esophagusMESH:D001749Urinary Bladder Neoplasmsbladder
HM01822SCPEP1esophagusMESH:D002318Cardiovascular Diseasesheart
HM01822SCPEP1esophagusMESH:D002318Cardiovascular Diseasesbone marrow
HM01822SCPEP1esophagusMESH:D002318Cardiovascular Diseasesblood vessel
HM01822SCPEP1esophagusMESH:D011537Pruritus
HM01822SCPEP1esophagusMESH:D000230Adenocarcinoma
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomauterus
HM01822SCPEP1esophagusMESH:D000230Adenocarcinoma
HM01822SCPEP1esophagusMESH:D000230Adenocarcinoma
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomauterus
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomathyroid
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomaskin
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomaparathyroid gland
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomaliver
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomakidney
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomaeye
HM01822SCPEP1esophagusMESH:D000230Adenocarcinomaadrenal gland
HM01822SCPEP1esophagusMESH:D004362Drug Toxicity
HM01822SCPEP1esophagusMESH:D015663Osteoporosis, Postmenopausal
HM01822SCPEP1esophagusMESH:D012512Sarcoma, Ewing's
HM01822SCPEP1esophagusMESH:D013119Spinal Cord Injuries
HM01822SCPEP1esophagusMESH:D001321Autistic Disorder
HM01822SCPEP1esophagusMESH:D017114Liver Failure, Acute
HM01822SCPEP1esophagusMESH:D055728Primary Myelofibrosisbone marrow
HM01822SCPEP1esophagusMESH:D000236Adenomapancreas
HM01822SCPEP1esophagusMESH:D000236Adenomaliver
HM01822SCPEP1esophagusMESH:D000236Adenomakidney
HM01822SCPEP1esophagusMESH:D000236Adenoma
HM01822SCPEP1esophagusMESH:D000236Adenoma
HM01822SCPEP1esophagusMESH:D000236Adenoma
HM01822SCPEP1esophagusMESH:D000236Adenoma
HM01822SCPEP1esophagusMESH:D009190Myelodysplastic Syndromes
HM01822SCPEP1esophagusMESH:D010190Pancreatic Neoplasmspancreas
HM01822SCPEP1esophagusMESH:D015459Leukemia-Lymphoma, Adult T-Cellbone marrow
HM01822SCPEP1esophagusMESH:D007951Leukemia, Myeloidbone marrow
HM01822SCPEP1esophagusMESH:D015477Leukemia, Myelomonocytic, Chronic
HM01822SCPEP1esophagusMESH:D008107Liver Diseasesskin
HM01822SCPEP1esophagusMESH:D008107Liver Diseasesmuscle
HM01822SCPEP1esophagusMESH:D008107Liver Diseaseslung
HM01822SCPEP1esophagusMESH:D008107Liver Diseasesliver
HM01822SCPEP1esophagusMESH:D000015Abnormalities, Multiple
HM01822SCPEP1esophagusMESH:D004938Esophageal Neoplasms
HM01822SCPEP1esophagusMESH:D015674Mammary Neoplasms, Animal
HM01822SCPEP1esophagusMESH:D010382Peliosis Hepatisliver
HM01822SCPEP1esophagusMESH:D009101Multiple Myelomabone marrow
HM01822SCPEP1esophagusMESH:D006869Hydronephrosiskidney
HM01822SCPEP1esophagusMESH:D017202Myocardial Ischemiaheart
HM01822SCPEP1esophagusMESH:D009364Neoplasm Recurrence, Local
HM01822SCPEP1esophagusMESH:D013274Stomach Neoplasms
HM01822SCPEP1esophagusMESH:D000799Angioedemaskin
HM01822SCPEP1esophagusMESH:D019636Neurodegenerative Diseasesnerve
HM01822SCPEP1esophagusMESH:D019851Thrombophiliabone marrow
HM01822SCPEP1esophagusMESH:D004701Endocrine Gland Neoplasmsthyroid
HM01822SCPEP1esophagusMESH:D004701Endocrine Gland Neoplasmspituitary
HM01822SCPEP1esophagusMESH:D004701Endocrine Gland Neoplasmsparathyroid gland
HM01822SCPEP1esophagusMESH:D004701Endocrine Gland Neoplasmsbrain
HM01822SCPEP1esophagusMESH:D004701Endocrine Gland Neoplasmsadrenal gland
HM01822SCPEP1esophagusMESH:D006470Hemorrhage
HM01822SCPEP1esophagusMESH:D006849Hydrocephalusbrain
HM01822SCPEP1esophagusMESH:D005313Fetal Death
HM01822SCPEP1esophagusMESH:D002972Cleft Palate
HM01822SCPEP1esophagusMESH:D004828Epilepsies, Partialmuscle
HM01822SCPEP1esophagusMESH:D015458Leukemia, T-Cellbone marrow
HM01822SCPEP1esophagusMESH:D013088Spermatocele
HM01822SCPEP1esophagusMESH:D014604Uveal Neoplasmseye
HM01822SCPEP1esophagusMESH:D004827Epilepsymuscle
HM01822SCPEP1esophagusMESH:D052776Female Urogenital Diseases
HM01822SCPEP1esophagusMESH:D007674Kidney Diseasesureter
HM01822SCPEP1esophagusMESH:D007674Kidney Diseasespituitary
HM01822SCPEP1esophagusMESH:D007674Kidney Diseaseskidney
HM01822SCPEP1esophagusMESH:D000550Amblyopiabrain
HM01822SCPEP1esophagusMESH:D000550Amblyopiabrain
HM01822SCPEP1esophagusMESH:D003110Colonic Neoplasmscolon
HM01822SCPEP1esophagusMESH:D005317Fetal Growth Retardation
HM01822SCPEP1esophagusMESH:D015464Leukemia, Myelogenous, Chronic, BCR-ABL Positivebone marrow
HM01822SCPEP1esophagusMESH:D008325Mammary Neoplasms, Experimental
HM01822SCPEP1esophagusMESH:D008881Migraine Disordersbrain
HM01822SCPEP1esophagusMESH:D001714Bipolar Disorder
HM01822SCPEP1esophagusMESH:D001848Bone Diseases, Developmental
HM01822SCPEP1esophagusMESH:D006973Hypertensionlung
HM01822SCPEP1esophagusMESH:D006973Hypertensionheart
HM01822SCPEP1esophagusMESH:D006973Hypertensionblood vessel
HM01822SCPEP1esophagusMESH:D012878Skin Neoplasms
HM01822SCPEP1esophagusMESH:D008106Liver Cirrhosis, Experimental
HM01822SCPEP1esophagusMESH:D011297Prenatal Exposure Delayed Effects
HM01822SCPEP1esophagusMESH:D054079Vascular Malformations
HM01822SCPEP1esophagusMESH:D018248Adenoma, Liver Cell
HM01822SCPEP1esophagusMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01822SCPEP1esophagusMESH:D013964Thyroid Neoplasmsthyroid
HM01822SCPEP1esophagusMESH:D006930Hyperalgesia
HM01822SCPEP1esophagusMESH:D008133Long QT Syndrome
HM01822SCPEP1esophagusMESH:D002294Carcinoma, Squamous Celllung
HM01822SCPEP1esophagusMESH:D002294Carcinoma, Squamous Cellliver
HM01822SCPEP1esophagusMESH:D002294Carcinoma, Squamous Celllarynx
HM01822SCPEP1esophagusMESH:D002294Carcinoma, Squamous Cellkidney
HM01822SCPEP1esophagusMESH:D002294Carcinoma, Squamous Celleye
HM01822SCPEP1esophagusMESH:D023903Coronary Restenosisheart
HM01822SCPEP1esophagusMESH:D005315Fetal Diseases
HM01822SCPEP1esophagusMESH:D009421Nervous System Malformations
HM01822SCPEP1esophagusMESH:D000014Abnormalities, Drug-Induced
HM01822SCPEP1esophagusMESH:D006330Heart Defects, Congenital
HM01822SCPEP1esophagusMESH:D014581Urticariaskin
HM01822SCPEP1esophagusMESH:D004487Edema
HM01822SCPEP1esophagusMESH:D005355Fibrosis
HM01822SCPEP1esophagusMESH:D007569Jaw Abnormalities
HM01822SCPEP1esophagusMESH:D013927Thrombosis
HM01822SCPEP1esophagusMESH:D000740Anemiabone marrow
HM01822SCPEP1esophagusMESH:D007948Leukemia, Monocytic, Acutebone marrow
HM01822SCPEP1esophagusMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM01822SCPEP1esophagusMESH:D005124Eye Abnormalities
HM01822SCPEP1esophagusMESH:D008175Lung Neoplasmslung
HM01822SCPEP1esophagusMESH:D002386Cataractpancreas
HM01822SCPEP1esophagusMESH:D002386Cataracteye
HM01822SCPEP1esophagusMESH:D005234Fatty Liver
HM01822SCPEP1esophagusMESH:D019465Craniofacial Abnormalities
HM01822SCPEP1esophagusMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01822SCPEP1esophagusMESH:D007021Hypospadias
HM01822SCPEP1esophagusMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01822SCPEP1esophagusMESH:D006528Carcinoma, Hepatocellularliver
HM01822SCPEP1esophagusMESH:D004421Dystonia
HM01822SCPEP1esophagusMESH:D017563Lung Diseases, Interstitiallung
HM01822SCPEP1esophagusMESH:D008546Melanoma, Experimental
HM01822SCPEP1esophagusMESH:D000008Abdominal Neoplasmsureter
HM01822SCPEP1esophagusMESH:D000008Abdominal Neoplasmsprostate
HM01822SCPEP1esophagusMESH:D000008Abdominal Neoplasmsliver
HM01822SCPEP1esophagusMESH:D000008Abdominal Neoplasmsbone
HM01822SCPEP1esophagusMESH:D000008Abdominal Neoplasmsbladder
HM01822SCPEP1esophagusMESH:D000013Congenital Abnormalities
HM01822SCPEP1esophagusMESH:D004714Endometrial Hyperplasia
HM01822SCPEP1esophagusMESH:D017029Epilepsy, Complex Partialmuscle
HM01822SCPEP1esophagusMESH:D009139Musculoskeletal Abnormalities
HM01822SCPEP1esophagusMESH:D009182Mycosis Fungoides
HM01822SCPEP1esophagusMESH:D009203Myocardial Infarctionheart
HM01822SCPEP1esophagusMESH:D002051Burkitt Lymphoma
HM01822SCPEP1esophagusMESH:D006332Cardiomegaly
HM01822SCPEP1esophagusMESH:D008114Liver Neoplasms, Experimental
HM01822SCPEP1esophagusMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01822SCPEP1esophagusMESH:D008113Liver Neoplasms
HM01822SCPEP1esophagusMESH:D008113Liver Neoplasms
HM01822SCPEP1esophagusMESH:D012208Rhabdomyosarcomarectum
HM01822SCPEP1esophagusMESH:D012208Rhabdomyosarcomaprostate
HM01822SCPEP1esophagusMESH:D012208Rhabdomyosarcomamuscle
HM01822SCPEP1esophagusMESH:D001008Anxiety Disorders
HM01822SCPEP1esophagusMESH:D007248Infertility, Male
HM01822SCPEP1esophagusMESH:D011471Prostatic Neoplasmsprostate
HM01822SCPEP1esophagusMESH:D013226Status Epilepticusmuscle
HM01822SCPEP1esophagusMESH:D013226Status Epilepticusmuscle
HM01822SCPEP1esophagusMESH:D013226Status Epilepticusmuscle
HM01822SCPEP1esophagusMESH:D019247HIV Wasting Syndrome
HM01822SCPEP1esophagusMESH:D012640Seizuresmuscle
HM01822SCPEP1esophagusMESH:D020246Venous Thrombosis
HM01822SCPEP1esophagusMESH:D005909Glioblastomabone
HM01822SCPEP1esophagusMESH:D005909Glioblastomabrain
HM01822SCPEP1esophagusMESH:D005909Glioblastomabone
HM01822SCPEP1esophagusMESH:D015428Myocardial Reperfusion Injury
HM01822SCPEP1esophagusMESH:D009361Neoplasm Invasiveness
HM01822SCPEP1esophagusMESH:D010235Paraganglioma
HM01822SCPEP1esophagusMESH:D013959Thyroid Diseasesthyroid
HM01822SCPEP1esophagusMESH:D018221Fibromatosis, Abdominal
HM01822SCPEP1esophagusMESH:D005706Gallbladder Neoplasmsliver
HM01822SCPEP1esophagusMESH:D005706Gallbladder Neoplasmsliver
HM01822SCPEP1esophagusMESH:D010146Pain
HM01822SCPEP1esophagusMESH:D001169Arthritis, Experimental
HM01822SCPEP1esophagusMESH:D016889Endometrial Neoplasmsuterus
HM01822SCPEP1esophagusMESH:D008103Liver Cirrhosisliver
HM01822SCPEP1esophagusMESH:D016135Spinal Dysraphismspinal cord
HM01822SCPEP1esophagusMESH:D002471Cell Transformation, Neoplastic
HM01822SCPEP1esophagusMESH:D002277Carcinoma
HM01822SCPEP1esophagusMESH:D007938Leukemiaspleen
HM01822SCPEP1esophagusMESH:D007938Leukemiabone marrow
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmsthyroid
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmsskin
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmsparathyroid gland
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmslarynx
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmsear
HM01822SCPEP1esophagusMESH:D006258Head and Neck Neoplasmsbrain
HM01822SCPEP1esophagusMESH:D014564Urogenital Abnormalities
HM01822SCPEP1esophagusMESH:D001161Arteriosclerosisblood vessel
HM01822SCPEP1esophagusMESH:D018222Fibromatosis, Aggressive
HM01822SCPEP1esophagusMESH:D008223Lymphoma
HM01822SCPEP1esophagusMESH:D001778Blood Coagulation Disordersbone marrow
HM01822SCPEP1esophagusMESH:D018328Melanoma, Amelanotic
HM01822SCPEP1esophagusMESH:D009436Neural Tube Defects
HM01822SCPEP1esophagusMESH:D011470Prostatic Hyperplasia
HM01822SCPEP1esophagusMESH:D000152Acne Vulgaris
HM01822SCPEP1esophagusMESH:D006529Hepatomegaly
HM01822SCPEP1esophagusMESH:D008064Lipidoses
HM01822SCPEP1esophagusMESH:D010024Osteoporosisbone
HM01822SCPEP1esophagusMESH:D015619Respiratory System Abnormalities
HM01822SCPEP1esophagusMESH:D012559Schizophrenia
HM01822SCPEP1esophagusMESH:D056486Drug-Induced Liver Injury
HM01822SCPEP1esophagusMESH:D007249Inflammation
HM01822SCPEP1esophagusMESH:D020149Manganese Poisoning
HM01822SCPEP1esophagusMESH:D019310Pseudolymphoma
HM01822SCPEP1esophagusMESH:D019282Wasting Syndrome
HM01822SCPEP1esophagusMESH:D016757Death, Sudden, Cardiac
HM01822SCPEP1esophagusMESH:D006965Hyperplasia
HM01822SCPEP1esophagusMESH:D007247Infertility, Female
HM01822SCPEP1esophagusMESH:D016584Panic Disorder
HM01822SCPEP1esophagusMESH:D004831Epilepsies, Myoclonicmuscle
HM01822SCPEP1esophagusMESH:D009362Neoplasm Metastasis
HM01822SCPEP1esophagusMESH:D011230Precancerous Conditions
HM01822SCPEP1esophagusMESH:D012871Skin Diseasesskin
HM01822SCPEP1esophagusMESH:D016171Torsades de Pointes
HM01822SCPEP1esophagusMESH:D015179Colorectal Neoplasms
HM01822SCPEP1esophagusMESH:D008545Melanomaeye
HM01822SCPEP1esophagusMESH:D008545Melanomacervix
HM01822SCPEP1esophagusMESH:D008545Melanomabone
HM01822SCPEP1esophagusMESH:D002779Cholestasisliver
HM01822SCPEP1esophagusMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01822SCPEP1esophagusMESH:D017119Porphyria Cutanea Tardaskin
HM01822SCPEP1esophagusMESH:D014178Translocation, Genetic
HM01822SCPEP1esophagusMESH:D018288Carcinoma, Small Cellprostate
HM01822SCPEP1esophagusMESH:D018288Carcinoma, Small Celllung
HM01822SCPEP1esophagusMESH:D018288Carcinoma, Small Cellliver
HM01822SCPEP1esophagusMESH:D018288Carcinoma, Small Celllarynx
HM01822SCPEP1esophagusMESH:D009369Neoplasmsspleen
HM01822SCPEP1esophagusMESH:D009369Neoplasmsbone marrow
HM01822SCPEP1esophagusMESH:D001943Breast Neoplasmsbreast
HM01822SCPEP1esophagusMESH:D018281Cholangiocarcinomaliver
HM01822SCPEP1esophagusMESH:D003928Diabetic Nephropathies
HM01822SCPEP1esophagusMESH:D014594Uterine Neoplasmscervix
HM01822SCPEP1esophagusMESH:D014594Uterine Neoplasms
HM01822SCPEP1esophagusMESH:D002291Carcinoma, Papillary
HM01822SCPEP1esophagusMESH:D010051Ovarian Neoplasmsuterus
HM01822SCPEP1esophagusMESH:D010051Ovarian Neoplasms
HM01822SCPEP1esophagusMESH:D004832Epilepsy, Absencemuscle