Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03102SLC17A5parathyroid glandMESH:D007674Kidney Diseasesureter
HM03102SLC17A5parathyroid glandMESH:D007674Kidney Diseasespituitary
HM03102SLC17A5parathyroid glandMESH:D007674Kidney Diseaseskidney
HM03102SLC17A5parathyroid glandMESH:D017563Lung Diseases, Interstitiallung
HM03102SLC17A5parathyroid glandMESH:D019465Craniofacial Abnormalities
HM03102SLC17A5parathyroid glandMESH:D004827Epilepsymuscle
HM03102SLC17A5parathyroid glandMESH:D016135Spinal Dysraphismspinal cord
HM03102SLC17A5parathyroid glandMESH:D012640Seizuresmuscle
HM03102SLC17A5parathyroid glandMESH:D001714Bipolar Disorder
HM03102SLC17A5parathyroid glandMESH:D008881Migraine Disordersbrain
HM03102SLC17A5parathyroid glandMESH:D009190Myelodysplastic Syndromes
HM03102SLC17A5parathyroid glandMESH:D014581Urticariaskin
HM03102SLC17A5parathyroid glandMESH:D009436Neural Tube Defects
HM03102SLC17A5parathyroid glandMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM03102SLC17A5parathyroid glandMESH:D020194Unverricht-Lundborg Syndromemuscle
HM03102SLC17A5parathyroid glandMESH:D000015Abnormalities, Multiple
HM03102SLC17A5parathyroid glandMESH:D001848Bone Diseases, Developmental
HM03102SLC17A5parathyroid glandMESH:D010146Pain
HM03102SLC17A5parathyroid glandMESH:D017029Epilepsy, Complex Partialmuscle
HM03102SLC17A5parathyroid glandMESH:D000550Amblyopiabrain
HM03102SLC17A5parathyroid glandMESH:D000550Amblyopiabrain
HM03102SLC17A5parathyroid glandMESH:D000799Angioedemaskin
HM03102SLC17A5parathyroid glandMESH:D004421Dystonia
HM03102SLC17A5parathyroid glandMESH:D002386Cataractpancreas
HM03102SLC17A5parathyroid glandMESH:D002386Cataracteye
HM03102SLC17A5parathyroid glandMESH:D056486Drug-Induced Liver Injury
HM03102SLC17A5parathyroid glandMESH:D004828Epilepsies, Partialmuscle
HM03102SLC17A5parathyroid glandMESH:D014564Urogenital Abnormalities
HM03102SLC17A5parathyroid glandMESH:D005234Fatty Liver
HM03102SLC17A5parathyroid glandMESH:D019310Pseudolymphoma
HM03102SLC17A5parathyroid glandMESH:D008546Melanoma, Experimental
HM03102SLC17A5parathyroid glandMESH:D019636Neurodegenerative Diseasesnerve
HM03102SLC17A5parathyroid glandMESH:D013226Status Epilepticusmuscle
HM03102SLC17A5parathyroid glandMESH:D013226Status Epilepticusmuscle
HM03102SLC17A5parathyroid glandMESH:D013226Status Epilepticusmuscle
HM03102SLC17A5parathyroid glandMESH:D000014Abnormalities, Drug-Induced
HM03102SLC17A5parathyroid glandMESH:D004832Epilepsy, Absencemuscle
HM03102SLC17A5parathyroid glandMESH:D029461Sialic Acid Storage Disease
HM03102SLC17A5parathyroid glandMESH:D012559Schizophrenia
HM03102SLC17A5parathyroid glandMESH:D005317Fetal Growth Retardation
HM03102SLC17A5parathyroid glandMESH:D005315Fetal Diseases
HM03102SLC17A5parathyroid glandMESH:D008107Liver Diseasesskin
HM03102SLC17A5parathyroid glandMESH:D008107Liver Diseasesmuscle
HM03102SLC17A5parathyroid glandMESH:D008107Liver Diseaseslung
HM03102SLC17A5parathyroid glandMESH:D008107Liver Diseasesliver
HM03102SLC17A5parathyroid glandMESH:D009139Musculoskeletal Abnormalities
HM03102SLC17A5parathyroid glandMESH:D001008Anxiety Disorders
HM03102SLC17A5parathyroid glandMESH:D012208Rhabdomyosarcomarectum
HM03102SLC17A5parathyroid glandMESH:D012208Rhabdomyosarcomaprostate
HM03102SLC17A5parathyroid glandMESH:D012208Rhabdomyosarcomamuscle
HM03102SLC17A5parathyroid glandMESH:D004831Epilepsies, Myoclonicmuscle
HM03102SLC17A5parathyroid glandMESH:D006930Hyperalgesia
HM03102SLC17A5parathyroid glandMESH:D006849Hydrocephalusbrain
HM03102SLC17A5parathyroid glandMESH:D001321Autistic Disorder
HM03102SLC17A5parathyroid glandMESH:D014178Translocation, Genetic
HM03102SLC17A5parathyroid glandMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM03102SLC17A5parathyroid glandMESH:D017114Liver Failure, Acute
HM03102SLC17A5parathyroid glandMESH:D015470Leukemia, Myeloid, Acutebone marrow