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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01625GABARAPthyroidMESH:D003928Diabetic Nephropathies
HM01625GABARAPthyroidMESH:D018200Mixed Tumor, Mullerianbone
HM01625GABARAPthyroidMESH:D011693Purpurabone marrow
HM01625GABARAPthyroidMESH:D013276Stomach Ulcer
HM01625GABARAPthyroidMESH:D008113Liver Neoplasms
HM01625GABARAPthyroidMESH:D008113Liver Neoplasms
HM01625GABARAPthyroidMESH:D009139Musculoskeletal Abnormalities
HM01625GABARAPthyroidMESH:D054556Venous Thromboembolism
HM01625GABARAPthyroidMESH:D002972Cleft Palate
HM01625GABARAPthyroidMESH:D014178Translocation, Genetic
HM01625GABARAPthyroidMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM01625GABARAPthyroidMESH:D005315Fetal Diseases
HM01625GABARAPthyroidMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01625GABARAPthyroidMESH:D003865Depressive Disorder, Major
HM01625GABARAPthyroidMESH:D007889Leiomyomamuscle
HM01625GABARAPthyroidMESH:D001321Autistic Disorder
HM01625GABARAPthyroidMESH:D000015Abnormalities, Multiple
HM01625GABARAPthyroidMESH:D002318Cardiovascular Diseasesheart
HM01625GABARAPthyroidMESH:D002318Cardiovascular Diseasesbone marrow
HM01625GABARAPthyroidMESH:D002318Cardiovascular Diseasesblood vessel
HM01625GABARAPthyroidMESH:D003139Common Cold
HM01625GABARAPthyroidMESH:D003072Cognition Disorders
HM01625GABARAPthyroidMESH:D001749Urinary Bladder Neoplasmsureter
HM01625GABARAPthyroidMESH:D001749Urinary Bladder Neoplasmsbladder
HM01625GABARAPthyroidMESH:D004487Edema
HM01625GABARAPthyroidMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01625GABARAPthyroidMESH:D012559Schizophrenia
HM01625GABARAPthyroidMESH:D004827Epilepsymuscle
HM01625GABARAPthyroidMESH:D004828Epilepsies, Partialmuscle
HM01625GABARAPthyroidMESH:D008107Liver Diseasesskin
HM01625GABARAPthyroidMESH:D008107Liver Diseasesmuscle
HM01625GABARAPthyroidMESH:D008107Liver Diseaseslung
HM01625GABARAPthyroidMESH:D008107Liver Diseasesliver
HM01625GABARAPthyroidMESH:D016135Spinal Dysraphismspinal cord
HM01625GABARAPthyroidMESH:D001008Anxiety Disorders
HM01625GABARAPthyroidMESH:D004421Dystonia
HM01625GABARAPthyroidMESH:D019465Craniofacial Abnormalities
HM01625GABARAPthyroidMESH:D006548Hernia, Diaphragmatic
HM01625GABARAPthyroidMESH:D006973Hypertensionlung
HM01625GABARAPthyroidMESH:D006973Hypertensionheart
HM01625GABARAPthyroidMESH:D006973Hypertensionblood vessel
HM01625GABARAPthyroidMESH:D009232Myxoma
HM01625GABARAPthyroidMESH:D013964Thyroid Neoplasmsthyroid
HM01625GABARAPthyroidMESH:D001848Bone Diseases, Developmental
HM01625GABARAPthyroidMESH:D006529Hepatomegaly
HM01625GABARAPthyroidMESH:D010024Osteoporosisbone
HM01625GABARAPthyroidMESH:D000550Amblyopiabrain
HM01625GABARAPthyroidMESH:D000550Amblyopiabrain
HM01625GABARAPthyroidMESH:D012174Retinitis Pigmentosamuscle
HM01625GABARAPthyroidMESH:D007569Jaw Abnormalities
HM01625GABARAPthyroidMESH:D004831Epilepsies, Myoclonicmuscle
HM01625GABARAPthyroidMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01625GABARAPthyroidMESH:D006331Heart Diseasesheart
HM01625GABARAPthyroidMESH:D000544Alzheimer Diseasenerve
HM01625GABARAPthyroidMESH:D008171Lung Diseases
HM01625GABARAPthyroidMESH:D011657Pulmonary Eosinophilialung
HM01625GABARAPthyroidMESH:D011657Pulmonary Eosinophilialung
HM01625GABARAPthyroidMESH:D011657Pulmonary Eosinophilialung
HM01625GABARAPthyroidMESH:D002295Carcinoma, Transitional Cell
HM01625GABARAPthyroidMESH:D017563Lung Diseases, Interstitiallung
HM01625GABARAPthyroidMESH:D056486Drug-Induced Liver Injury
HM01625GABARAPthyroidMESH:D006849Hydrocephalusbrain
HM01625GABARAPthyroidMESH:D000014Abnormalities, Drug-Induced
HM01625GABARAPthyroidMESH:D008881Migraine Disordersbrain
HM01625GABARAPthyroidMESH:D014564Urogenital Abnormalities
HM01625GABARAPthyroidMESH:D014846Vulvar Neoplasms
HM01625GABARAPthyroidMESH:D001714Bipolar Disorder
HM01625GABARAPthyroidMESH:D001930Brain Injuries
HM01625GABARAPthyroidMESH:D004681Encephalomyelitis, Autoimmune, Experimental
HM01625GABARAPthyroidMESH:D004832Epilepsy, Absencemuscle
HM01625GABARAPthyroidMESH:D008114Liver Neoplasms, Experimental
HM01625GABARAPthyroidMESH:D011471Prostatic Neoplasmsprostate
HM01625GABARAPthyroidMESH:D005317Fetal Growth Retardation
HM01625GABARAPthyroidMESH:D009101Multiple Myelomabone marrow
HM01625GABARAPthyroidMESH:D009765Obesity
HM01625GABARAPthyroidMESH:D012640Seizuresmuscle
HM01625GABARAPthyroidMESH:D020521Strokeblood vessel
HM01625GABARAPthyroidMESH:D009436Neural Tube Defects
HM01625GABARAPthyroidMESH:D015663Osteoporosis, Postmenopausal
HM01625GABARAPthyroidMESH:D009190Myelodysplastic Syndromes
HM01625GABARAPthyroidMESH:D019310Pseudolymphoma
HM01625GABARAPthyroidMESH:D017029Epilepsy, Complex Partialmuscle
HM01625GABARAPthyroidMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01625GABARAPthyroidMESH:D008175Lung Neoplasmslung
HM01625GABARAPthyroidMESH:D006330Heart Defects, Congenital
HM01625GABARAPthyroidMESH:D005234Fatty Liver
HM01625GABARAPthyroidMESH:D012208Rhabdomyosarcomarectum
HM01625GABARAPthyroidMESH:D012208Rhabdomyosarcomaprostate
HM01625GABARAPthyroidMESH:D012208Rhabdomyosarcomamuscle
HM01625GABARAPthyroidMESH:D000419Albuminuria
HM01625GABARAPthyroidMESH:D001943Breast Neoplasmsbreast
HM01625GABARAPthyroidMESH:D013226Status Epilepticusmuscle
HM01625GABARAPthyroidMESH:D013226Status Epilepticusmuscle
HM01625GABARAPthyroidMESH:D013226Status Epilepticusmuscle