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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM02754AQPEPplacentaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM02754AQPEPplacentaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM02754AQPEPplacentaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM02754AQPEPplacentaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM02754AQPEPplacentaMESH:D007674Kidney Diseasesureter
HM02754AQPEPplacentaMESH:D007674Kidney Diseasespituitary
HM02754AQPEPplacentaMESH:D007674Kidney Diseaseskidney
HM02754AQPEPplacentaMESH:D005355Fibrosis
HM02754AQPEPplacentaMESH:D006973Hypertensionlung
HM02754AQPEPplacentaMESH:D006973Hypertensionheart
HM02754AQPEPplacentaMESH:D006973Hypertensionblood vessel
HM02754AQPEPplacentaMESH:D007638Keratoconjunctivitis Siccaeye
HM02754AQPEPplacentaMESH:D011565Psoriasisskin
HM02754AQPEPplacentaMESH:D005885Gingival Hyperplasia
HM02754AQPEPplacentaMESH:D006457Hemoglobinuria, Paroxysmal
HM02754AQPEPplacentaMESH:D009404Nephrotic Syndromekidney
HM02754AQPEPplacentaMESH:D014985Xerophthalmiaeye
HM02754AQPEPplacentaMESH:D009402Nephrosis, Lipoidkidney
HM02754AQPEPplacentaMESH:D014605Uveitiseye