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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01652SELPLGbloodMESH:D011833Radiation Injuries, Experimental
HM01652SELPLGbloodMESH:D001848Bone Diseases, Developmental
HM01652SELPLGbloodMESH:D008106Liver Cirrhosis, Experimental
HM01652SELPLGbloodMESH:D009410Nerve Degeneration
HM01652SELPLGbloodMESH:D008569Memory Disorders
HM01652SELPLGbloodMESH:D009203Myocardial Infarctionheart
HM01652SELPLGbloodMESH:D007154Immune System Diseases
HM01652SELPLGbloodMESH:D008546Melanoma, Experimental
HM01652SELPLGbloodMESH:D011471Prostatic Neoplasmsprostate
HM01652SELPLGbloodMESH:D013276Stomach Ulcer
HM01652SELPLGbloodMESH:D006849Hydrocephalusbrain
HM01652SELPLGbloodMESH:D006331Heart Diseasesheart
HM01652SELPLGbloodMESH:D006967Hypersensitivitybone marrow
HM01652SELPLGbloodMESH:D001943Breast Neoplasmsbreast
HM01652SELPLGbloodMESH:D019465Craniofacial Abnormalities
HM01652SELPLGbloodMESH:D007249Inflammation
HM01652SELPLGbloodMESH:D007674Kidney Diseasesureter
HM01652SELPLGbloodMESH:D007674Kidney Diseasespituitary
HM01652SELPLGbloodMESH:D007674Kidney Diseaseskidney
HM01652SELPLGbloodMESH:D017114Liver Failure, Acute
HM01652SELPLGbloodMESH:D010300Parkinson Diseasenerve
HM01652SELPLGbloodMESH:D001161Arteriosclerosisblood vessel
HM01652SELPLGbloodMESH:D007859Learning Disorders
HM01652SELPLGbloodMESH:D012208Rhabdomyosarcomarectum
HM01652SELPLGbloodMESH:D012208Rhabdomyosarcomaprostate
HM01652SELPLGbloodMESH:D012208Rhabdomyosarcomamuscle
HM01652SELPLGbloodMESH:D005355Fibrosis
HM01652SELPLGbloodMESH:D010146Pain
HM01652SELPLGbloodMESH:D012772Shock, Septic
HM01652SELPLGbloodMESH:D003928Diabetic Nephropathies
HM01652SELPLGbloodMESH:D004831Epilepsies, Myoclonicmuscle
HM01652SELPLGbloodMESH:D007511Ischemiaspinal cord
HM01652SELPLGbloodMESH:D007511Ischemiamuscle
HM01652SELPLGbloodMESH:D007511Ischemiaheart
HM01652SELPLGbloodMESH:D007511Ischemiaeye
HM01652SELPLGbloodMESH:D007511Ischemiablood vessel
HM01652SELPLGbloodMESH:D005315Fetal Diseases
HM01652SELPLGbloodMESH:D004827Epilepsymuscle
HM01652SELPLGbloodMESH:D000799Angioedemaskin
HM01652SELPLGbloodMESH:D007333Insulin Resistance
HM01652SELPLGbloodMESH:D004832Epilepsy, Absencemuscle
HM01652SELPLGbloodMESH:D014235Trichinellosis
HM01652SELPLGbloodMESH:D003092Colitis
HM01652SELPLGbloodMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM01652SELPLGbloodMESH:D001008Anxiety Disorders
HM01652SELPLGbloodMESH:D006946Hyperinsulinismpancreas
HM01652SELPLGbloodMESH:D012640Seizuresmuscle
HM01652SELPLGbloodMESH:D003457Cryptosporidiosis
HM01652SELPLGbloodMESH:D008175Lung Neoplasmslung
HM01652SELPLGbloodMESH:D008325Mammary Neoplasms, Experimental
HM01652SELPLGbloodMESH:D008881Migraine Disordersbrain
HM01652SELPLGbloodMESH:D016135Spinal Dysraphismspinal cord
HM01652SELPLGbloodMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01652SELPLGbloodMESH:D008103Liver Cirrhosisliver
HM01652SELPLGbloodMESH:D008654Mesotheliomabone
HM01652SELPLGbloodMESH:D003920Diabetes Mellituspancreas
HM01652SELPLGbloodMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01652SELPLGbloodMESH:D024821Metabolic Syndrome X
HM01652SELPLGbloodMESH:D009765Obesity
HM01652SELPLGbloodMESH:D014564Urogenital Abnormalities
HM01652SELPLGbloodMESH:D003921Diabetes Mellitus, Experimental
HM01652SELPLGbloodMESH:D050171Dyslipidemias
HM01652SELPLGbloodMESH:D004487Edema
HM01652SELPLGbloodMESH:D005234Fatty Liver
HM01652SELPLGbloodMESH:D006949Hyperlipidemias
HM01652SELPLGbloodMESH:D009139Musculoskeletal Abnormalities
HM01652SELPLGbloodMESH:D009190Myelodysplastic Syndromes
HM01652SELPLGbloodMESH:D009436Neural Tube Defects
HM01652SELPLGbloodMESH:D006561Herpes Simplex
HM01652SELPLGbloodMESH:D019636Neurodegenerative Diseasesnerve
HM01652SELPLGbloodMESH:D000015Abnormalities, Multiple
HM01652SELPLGbloodMESH:D010518Periodontitismouth
HM01652SELPLGbloodMESH:D017563Lung Diseases, Interstitiallung
HM01652SELPLGbloodMESH:D019310Pseudolymphoma
HM01652SELPLGbloodMESH:D000550Amblyopiabrain
HM01652SELPLGbloodMESH:D000550Amblyopiabrain
HM01652SELPLGbloodMESH:D002386Cataractpancreas
HM01652SELPLGbloodMESH:D002386Cataracteye
HM01652SELPLGbloodMESH:D014178Translocation, Genetic
HM01652SELPLGbloodMESH:D056486Drug-Induced Liver Injury
HM01652SELPLGbloodMESH:D008107Liver Diseasesskin
HM01652SELPLGbloodMESH:D008107Liver Diseasesmuscle
HM01652SELPLGbloodMESH:D008107Liver Diseaseslung
HM01652SELPLGbloodMESH:D008107Liver Diseasesliver
HM01652SELPLGbloodMESH:D000544Alzheimer Diseasenerve
HM01652SELPLGbloodMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM01652SELPLGbloodMESH:D017029Epilepsy, Complex Partialmuscle
HM01652SELPLGbloodMESH:D000707Anaphylaxis
HM01652SELPLGbloodMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01652SELPLGbloodMESH:D005317Fetal Growth Retardation
HM01652SELPLGbloodMESH:D015464Leukemia, Myelogenous, Chronic, BCR-ABL Positivebone marrow
HM01652SELPLGbloodMESH:D007248Infertility, Male
HM01652SELPLGbloodMESH:D014581Urticariaskin
HM01652SELPLGbloodMESH:D000382Agricultural Workers' Diseases
HM01652SELPLGbloodMESH:D004828Epilepsies, Partialmuscle
HM01652SELPLGbloodMESH:D004421Dystonia
HM01652SELPLGbloodMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01652SELPLGbloodMESH:D019457Chromosome Breakage
HM01652SELPLGbloodMESH:D006930Hyperalgesia
HM01652SELPLGbloodMESH:D050197Atherosclerosiskidney
HM01652SELPLGbloodMESH:D050197Atherosclerosisheart
HM01652SELPLGbloodMESH:D050197Atherosclerosisblood vessel
HM01652SELPLGbloodMESH:D012559Schizophrenia
HM01652SELPLGbloodMESH:D001321Autistic Disorder
HM01652SELPLGbloodMESH:D016393Lymphoma, B-Cell
HM01652SELPLGbloodMESH:D012135Respiratory Sounds
HM01652SELPLGbloodMESH:D001862Bone Resorption
HM01652SELPLGbloodMESH:D013226Status Epilepticusmuscle
HM01652SELPLGbloodMESH:D013226Status Epilepticusmuscle
HM01652SELPLGbloodMESH:D013226Status Epilepticusmuscle
HM01652SELPLGbloodMESH:D000014Abnormalities, Drug-Induced
HM01652SELPLGbloodMESH:D001714Bipolar Disorder