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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05181TMEM167Bparathyroid glandMESH:D014605Uveitiseye
HM05181TMEM167Bparathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05181TMEM167Bparathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05181TMEM167Bparathyroid glandMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05181TMEM167Bparathyroid glandMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05181TMEM167Bparathyroid glandMESH:D007674Kidney Diseasesureter
HM05181TMEM167Bparathyroid glandMESH:D007674Kidney Diseasespituitary
HM05181TMEM167Bparathyroid glandMESH:D007674Kidney Diseaseskidney
HM05181TMEM167Bparathyroid glandMESH:D006930Hyperalgesia
HM05181TMEM167Bparathyroid glandMESH:D014985Xerophthalmiaeye
HM05181TMEM167Bparathyroid glandMESH:D056487Drug-Induced Liver Injury, Chronicliver
HM05181TMEM167Bparathyroid glandMESH:D017114Liver Failure, Acute
HM05181TMEM167Bparathyroid glandMESH:D000799Angioedemaskin
HM05181TMEM167Bparathyroid glandMESH:D002386Cataractpancreas
HM05181TMEM167Bparathyroid glandMESH:D002386Cataracteye
HM05181TMEM167Bparathyroid glandMESH:D019636Neurodegenerative Diseasesnerve
HM05181TMEM167Bparathyroid glandMESH:D005355Fibrosis
HM05181TMEM167Bparathyroid glandMESH:D008107Liver Diseasesskin
HM05181TMEM167Bparathyroid glandMESH:D008107Liver Diseasesmuscle
HM05181TMEM167Bparathyroid glandMESH:D008107Liver Diseaseslung
HM05181TMEM167Bparathyroid glandMESH:D008107Liver Diseasesliver
HM05181TMEM167Bparathyroid glandMESH:D009402Nephrosis, Lipoidkidney
HM05181TMEM167Bparathyroid glandMESH:D010146Pain
HM05181TMEM167Bparathyroid glandMESH:D008546Melanoma, Experimental
HM05181TMEM167Bparathyroid glandMESH:D056486Drug-Induced Liver Injury
HM05181TMEM167Bparathyroid glandMESH:D006973Hypertensionlung
HM05181TMEM167Bparathyroid glandMESH:D006973Hypertensionheart
HM05181TMEM167Bparathyroid glandMESH:D006973Hypertensionblood vessel
HM05181TMEM167Bparathyroid glandMESH:D007638Keratoconjunctivitis Siccaeye
HM05181TMEM167Bparathyroid glandMESH:D009404Nephrotic Syndromekidney
HM05181TMEM167Bparathyroid glandMESH:D005885Gingival Hyperplasia
HM05181TMEM167Bparathyroid glandMESH:D006457Hemoglobinuria, Paroxysmal
HM05181TMEM167Bparathyroid glandMESH:D014581Urticariaskin
HM05181TMEM167Bparathyroid glandMESH:D001321Autistic Disorder
HM05181TMEM167Bparathyroid glandMESH:D011565Psoriasisskin