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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05080ARHGAP26mouthMESH:D054429Leukemia, Myelomonocytic, Juvenilebone marrow
HM05080ARHGAP26mouthMESH:D014591Uterine Diseasesuterus
HM05080ARHGAP26mouthMESH:D014591Uterine Diseasesplacenta
HM05080ARHGAP26mouthMESH:D014591Uterine Diseasescervix
HM05080ARHGAP26mouthMESH:D011297Prenatal Exposure Delayed Effects
HM05080ARHGAP26mouthMESH:D009436Neural Tube Defects
HM05080ARHGAP26mouthMESH:D001321Autistic Disorder
HM05080ARHGAP26mouthMESH:D019310Pseudolymphoma
HM05080ARHGAP26mouthMESH:D014605Uveitiseye
HM05080ARHGAP26mouthMESH:D000230Adenocarcinoma
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomauterus
HM05080ARHGAP26mouthMESH:D000230Adenocarcinoma
HM05080ARHGAP26mouthMESH:D000230Adenocarcinoma
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomauterus
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomathyroid
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomaskin
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomaparathyroid gland
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomaliver
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomakidney
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomaeye
HM05080ARHGAP26mouthMESH:D000230Adenocarcinomaadrenal gland
HM05080ARHGAP26mouthMESH:D005355Fibrosis
HM05080ARHGAP26mouthMESH:D009765Obesity
HM05080ARHGAP26mouthMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05080ARHGAP26mouthMESH:D004832Epilepsy, Absencemuscle
HM05080ARHGAP26mouthMESH:D014178Translocation, Genetic
HM05080ARHGAP26mouthMESH:D000550Amblyopiabrain
HM05080ARHGAP26mouthMESH:D000550Amblyopiabrain
HM05080ARHGAP26mouthMESH:D013274Stomach Neoplasms
HM05080ARHGAP26mouthMESH:D011471Prostatic Neoplasmsprostate
HM05080ARHGAP26mouthMESH:D000015Abnormalities, Multiple
HM05080ARHGAP26mouthMESH:D008175Lung Neoplasmslung
HM05080ARHGAP26mouthMESH:D007333Insulin Resistance
HM05080ARHGAP26mouthMESH:D012878Skin Neoplasms
HM05080ARHGAP26mouthMESH:D014564Urogenital Abnormalities
HM05080ARHGAP26mouthMESH:D017563Lung Diseases, Interstitiallung
HM05080ARHGAP26mouthMESH:D004827Epilepsymuscle
HM05080ARHGAP26mouthMESH:D007249Inflammation
HM05080ARHGAP26mouthMESH:D056486Drug-Induced Liver Injury
HM05080ARHGAP26mouthMESH:D001749Urinary Bladder Neoplasmsureter
HM05080ARHGAP26mouthMESH:D001749Urinary Bladder Neoplasmsbladder
HM05080ARHGAP26mouthMESH:D006330Heart Defects, Congenital
HM05080ARHGAP26mouthMESH:D006849Hydrocephalusbrain
HM05080ARHGAP26mouthMESH:D001714Bipolar Disorder
HM05080ARHGAP26mouthMESH:D004828Epilepsies, Partialmuscle
HM05080ARHGAP26mouthMESH:D009062Mouth Neoplasms
HM05080ARHGAP26mouthMESH:D001008Anxiety Disorders
HM05080ARHGAP26mouthMESH:D012640Seizuresmuscle
HM05080ARHGAP26mouthMESH:D008664Metal Metabolism, Inborn Errorsskin
HM05080ARHGAP26mouthMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM05080ARHGAP26mouthMESH:D008664Metal Metabolism, Inborn Errorsliver
HM05080ARHGAP26mouthMESH:D008664Metal Metabolism, Inborn Errorskidney
HM05080ARHGAP26mouthMESH:D002278Carcinoma in Situ
HM05080ARHGAP26mouthMESH:D002278Carcinoma in Situ
HM05080ARHGAP26mouthMESH:D004421Dystonia
HM05080ARHGAP26mouthMESH:D008103Liver Cirrhosisliver
HM05080ARHGAP26mouthMESH:D000014Abnormalities, Drug-Induced
HM05080ARHGAP26mouthMESH:D009402Nephrosis, Lipoidkidney
HM05080ARHGAP26mouthMESH:D009421Nervous System Malformations
HM05080ARHGAP26mouthMESH:D011565Psoriasisskin
HM05080ARHGAP26mouthMESH:D011629Puberty, Precocious
HM05080ARHGAP26mouthMESH:D019465Craniofacial Abnormalities
HM05080ARHGAP26mouthMESH:D005234Fatty Liver
HM05080ARHGAP26mouthMESH:D006973Hypertensionlung
HM05080ARHGAP26mouthMESH:D006973Hypertensionheart
HM05080ARHGAP26mouthMESH:D006973Hypertensionblood vessel
HM05080ARHGAP26mouthMESH:D001848Bone Diseases, Developmental
HM05080ARHGAP26mouthMESH:D001943Breast Neoplasmsbreast
HM05080ARHGAP26mouthMESH:D009404Nephrotic Syndromekidney
HM05080ARHGAP26mouthMESH:D013226Status Epilepticusmuscle
HM05080ARHGAP26mouthMESH:D013226Status Epilepticusmuscle
HM05080ARHGAP26mouthMESH:D013226Status Epilepticusmuscle
HM05080ARHGAP26mouthMESH:D019966Substance-Related Disorders
HM05080ARHGAP26mouthMESH:D050171Dyslipidemias
HM05080ARHGAP26mouthMESH:D007674Kidney Diseasesureter
HM05080ARHGAP26mouthMESH:D007674Kidney Diseasespituitary
HM05080ARHGAP26mouthMESH:D007674Kidney Diseaseskidney
HM05080ARHGAP26mouthMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05080ARHGAP26mouthMESH:D005315Fetal Diseases
HM05080ARHGAP26mouthMESH:D008881Migraine Disordersbrain
HM05080ARHGAP26mouthMESH:D004938Esophageal Neoplasms
HM05080ARHGAP26mouthMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05080ARHGAP26mouthMESH:D005317Fetal Growth Retardation
HM05080ARHGAP26mouthMESH:D004831Epilepsies, Myoclonicmuscle
HM05080ARHGAP26mouthMESH:D005885Gingival Hyperplasia
HM05080ARHGAP26mouthMESH:D009190Myelodysplastic Syndromes
HM05080ARHGAP26mouthMESH:D012559Schizophrenia
HM05080ARHGAP26mouthMESH:D006457Hemoglobinuria, Paroxysmal
HM05080ARHGAP26mouthMESH:D001161Arteriosclerosisblood vessel
HM05080ARHGAP26mouthMESH:D017029Epilepsy, Complex Partialmuscle
HM05080ARHGAP26mouthMESH:D016135Spinal Dysraphismspinal cord
HM05080ARHGAP26mouthMESH:D008113Liver Neoplasms
HM05080ARHGAP26mouthMESH:D008113Liver Neoplasms
HM05080ARHGAP26mouthMESH:D002294Carcinoma, Squamous Celllung
HM05080ARHGAP26mouthMESH:D002294Carcinoma, Squamous Cellliver
HM05080ARHGAP26mouthMESH:D002294Carcinoma, Squamous Celllarynx
HM05080ARHGAP26mouthMESH:D002294Carcinoma, Squamous Cellkidney
HM05080ARHGAP26mouthMESH:D002294Carcinoma, Squamous Celleye
HM05080ARHGAP26mouthMESH:D007638Keratoconjunctivitis Siccaeye
HM05080ARHGAP26mouthMESH:D009139Musculoskeletal Abnormalities
HM05080ARHGAP26mouthMESH:D010049Ovarian Diseasesovary
HM05080ARHGAP26mouthMESH:D001862Bone Resorption
HM05080ARHGAP26mouthMESH:D012208Rhabdomyosarcomarectum
HM05080ARHGAP26mouthMESH:D012208Rhabdomyosarcomaprostate
HM05080ARHGAP26mouthMESH:D012208Rhabdomyosarcomamuscle
HM05080ARHGAP26mouthMESH:D014985Xerophthalmiaeye