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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00532VGLL3placentaMESH:D058186Acute Kidney Injury
HM00532VGLL3placentaMESH:D006973Hypertensionlung
HM00532VGLL3placentaMESH:D006973Hypertensionheart
HM00532VGLL3placentaMESH:D006973Hypertensionblood vessel
HM00532VGLL3placentaMESH:D005234Fatty Liver
HM00532VGLL3placentaMESH:D001943Breast Neoplasmsbreast
HM00532VGLL3placentaMESH:D008106Liver Cirrhosis, Experimental
HM00532VGLL3placentaMESH:D017114Liver Failure, Acute
HM00532VGLL3placentaMESH:D056486Drug-Induced Liver Injury
HM00532VGLL3placentaMESH:D006528Carcinoma, Hepatocellularliver
HM00532VGLL3placentaMESH:D013118Spinal Cord Diseasesspinal cord
HM00532VGLL3placentaMESH:D015179Colorectal Neoplasms
HM00532VGLL3placentaMESH:D005355Fibrosis
HM00532VGLL3placentaMESH:D002318Cardiovascular Diseasesheart
HM00532VGLL3placentaMESH:D002318Cardiovascular Diseasesbone marrow
HM00532VGLL3placentaMESH:D002318Cardiovascular Diseasesblood vessel
HM00532VGLL3placentaMESH:D016889Endometrial Neoplasmsuterus
HM00532VGLL3placentaMESH:D006330Heart Defects, Congenital
HM00532VGLL3placentaMESH:D009436Neural Tube Defects
HM00532VGLL3placentaMESH:D003924Diabetes Mellitus, Type 2pancreas
HM00532VGLL3placentaMESH:D000544Alzheimer Diseasenerve
HM00532VGLL3placentaMESH:D009503Neutropeniabone marrow
HM00532VGLL3placentaMESH:D009404Nephrotic Syndromekidney
HM00532VGLL3placentaMESH:D006679HIV Seropositivity
HM00532VGLL3placentaMESH:D020138Hyperhomocysteinemia
HM00532VGLL3placentaMESH:D011565Psoriasisskin
HM00532VGLL3placentaMESH:D002972Cleft Palate
HM00532VGLL3placentaMESH:D014605Uveitiseye
HM00532VGLL3placentaMESH:D008107Liver Diseasesskin
HM00532VGLL3placentaMESH:D008107Liver Diseasesmuscle
HM00532VGLL3placentaMESH:D008107Liver Diseaseslung
HM00532VGLL3placentaMESH:D008107Liver Diseasesliver
HM00532VGLL3placentaMESH:D020521Strokeblood vessel
HM00532VGLL3placentaMESH:D008180Lupus Erythematosus, Systemicbone marrow
HM00532VGLL3placentaMESH:D017093Liver Failure
HM00532VGLL3placentaMESH:D006457Hemoglobinuria, Paroxysmal
HM00532VGLL3placentaMESH:D012559Schizophrenia
HM00532VGLL3placentaMESH:D008175Lung Neoplasmslung
HM00532VGLL3placentaMESH:D007638Keratoconjunctivitis Siccaeye
HM00532VGLL3placentaMESH:D008114Liver Neoplasms, Experimental
HM00532VGLL3placentaMESH:D008664Metal Metabolism, Inborn Errorsskin
HM00532VGLL3placentaMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM00532VGLL3placentaMESH:D008664Metal Metabolism, Inborn Errorsliver
HM00532VGLL3placentaMESH:D008664Metal Metabolism, Inborn Errorskidney
HM00532VGLL3placentaMESH:D002252Carbon Tetrachloride Poisoning
HM00532VGLL3placentaMESH:D006932Hyperbilirubinemia
HM00532VGLL3placentaMESH:D005901Glaucomaeye
HM00532VGLL3placentaMESH:D005885Gingival Hyperplasia
HM00532VGLL3placentaMESH:D006505Hepatitis
HM00532VGLL3placentaMESH:D005756Gastritis
HM00532VGLL3placentaMESH:D008103Liver Cirrhosisliver
HM00532VGLL3placentaMESH:D017889Exfoliation Syndromeeye
HM00532VGLL3placentaMESH:D000236Adenomapancreas
HM00532VGLL3placentaMESH:D000236Adenomaliver
HM00532VGLL3placentaMESH:D000236Adenomakidney
HM00532VGLL3placentaMESH:D000236Adenoma
HM00532VGLL3placentaMESH:D000236Adenoma
HM00532VGLL3placentaMESH:D000236Adenoma
HM00532VGLL3placentaMESH:D000236Adenoma
HM00532VGLL3placentaMESH:D051437Renal Insufficiency
HM00532VGLL3placentaMESH:D013274Stomach Neoplasms
HM00532VGLL3placentaMESH:D014985Xerophthalmiaeye
HM00532VGLL3placentaMESH:D009402Nephrosis, Lipoidkidney
HM00532VGLL3placentaMESH:D007674Kidney Diseasesureter
HM00532VGLL3placentaMESH:D007674Kidney Diseasespituitary
HM00532VGLL3placentaMESH:D007674Kidney Diseaseskidney
HM00532VGLL3placentaMESH:D008113Liver Neoplasms
HM00532VGLL3placentaMESH:D008113Liver Neoplasms
HM00532VGLL3placentaMESH:D019767Maxillofacial Abnormalities