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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00877TIMM50pancreasMESH:D001714Bipolar Disorder
HM00877TIMM50pancreasMESH:D004832Epilepsy, Absencemuscle
HM00877TIMM50pancreasMESH:D019310Pseudolymphoma
HM00877TIMM50pancreasMESH:D020194Unverricht-Lundborg Syndromemuscle
HM00877TIMM50pancreasMESH:D000550Amblyopiabrain
HM00877TIMM50pancreasMESH:D000550Amblyopiabrain
HM00877TIMM50pancreasMESH:D008881Migraine Disordersbrain
HM00877TIMM50pancreasMESH:D001848Bone Diseases, Developmental
HM00877TIMM50pancreasMESH:D012559Schizophrenia
HM00877TIMM50pancreasMESH:D004827Epilepsymuscle
HM00877TIMM50pancreasMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM00877TIMM50pancreasMESH:D009190Myelodysplastic Syndromes
HM00877TIMM50pancreasMESH:D004831Epilepsies, Myoclonicmuscle
HM00877TIMM50pancreasMESH:D000015Abnormalities, Multiple
HM00877TIMM50pancreasMESH:D009139Musculoskeletal Abnormalities
HM00877TIMM50pancreasMESH:D017563Lung Diseases, Interstitiallung
HM00877TIMM50pancreasMESH:D013226Status Epilepticusmuscle
HM00877TIMM50pancreasMESH:D013226Status Epilepticusmuscle
HM00877TIMM50pancreasMESH:D013226Status Epilepticusmuscle
HM00877TIMM50pancreasMESH:D012640Seizuresmuscle
HM00877TIMM50pancreasMESH:D005234Fatty Liver
HM00877TIMM50pancreasMESH:D016135Spinal Dysraphismspinal cord
HM00877TIMM50pancreasMESH:D019465Craniofacial Abnormalities
HM00877TIMM50pancreasMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM00877TIMM50pancreasMESH:D000014Abnormalities, Drug-Induced
HM00877TIMM50pancreasMESH:D009369Neoplasmsspleen
HM00877TIMM50pancreasMESH:D009369Neoplasmsbone marrow
HM00877TIMM50pancreasMESH:D009436Neural Tube Defects
HM00877TIMM50pancreasMESH:D046110Hypertension, Pregnancy-Inducedblood vessel
HM00877TIMM50pancreasMESH:D004828Epilepsies, Partialmuscle
HM00877TIMM50pancreasMESH:D012208Rhabdomyosarcomarectum
HM00877TIMM50pancreasMESH:D012208Rhabdomyosarcomaprostate
HM00877TIMM50pancreasMESH:D012208Rhabdomyosarcomamuscle
HM00877TIMM50pancreasMESH:D005317Fetal Growth Retardation
HM00877TIMM50pancreasMESH:D014178Translocation, Genetic
HM00877TIMM50pancreasMESH:D001008Anxiety Disorders
HM00877TIMM50pancreasMESH:D004421Dystonia
HM00877TIMM50pancreasMESH:D005315Fetal Diseases
HM00877TIMM50pancreasMESH:D006849Hydrocephalusbrain
HM00877TIMM50pancreasMESH:D014564Urogenital Abnormalities
HM00877TIMM50pancreasMESH:D017029Epilepsy, Complex Partialmuscle
HM00877TIMM50pancreasMESH:D056486Drug-Induced Liver Injury
HM00877TIMM50pancreasMESH:D001321Autistic Disorder