Homer

Gene HMID	Gene Symbol	Organ Specificity	DiseaseID	Disease Name	Related Organ
HM03478	B4GALT4	esophagus	MESH:D004832	Epilepsy, Absence	muscle
HM03478	B4GALT4	esophagus	MESH:D015470	Leukemia, Myeloid, Acute	bone marrow
HM03478	B4GALT4	esophagus	MESH:D015428	Myocardial Reperfusion Injury
HM03478	B4GALT4	esophagus	MESH:D018248	Adenoma, Liver Cell
HM03478	B4GALT4	esophagus	MESH:D009190	Myelodysplastic Syndromes
HM03478	B4GALT4	esophagus	MESH:D000014	Abnormalities, Drug-Induced
HM03478	B4GALT4	esophagus	MESH:D008113	Liver Neoplasms
HM03478	B4GALT4	esophagus	MESH:D008113	Liver Neoplasms
HM03478	B4GALT4	esophagus	MESH:D020194	Unverricht-Lundborg Syndrome	muscle
HM03478	B4GALT4	esophagus	MESH:D007333	Insulin Resistance
HM03478	B4GALT4	esophagus	MESH:D019310	Pseudolymphoma
HM03478	B4GALT4	esophagus	MESH:D001008	Anxiety Disorders
HM03478	B4GALT4	esophagus	MESH:D015427	Reperfusion Injury
HM03478	B4GALT4	esophagus	MESH:D017563	Lung Diseases, Interstitial	lung
HM03478	B4GALT4	esophagus	MESH:D011471	Prostatic Neoplasms	prostate
HM03478	B4GALT4	esophagus	MESH:D013226	Status Epilepticus	muscle
HM03478	B4GALT4	esophagus	MESH:D013226	Status Epilepticus	muscle
HM03478	B4GALT4	esophagus	MESH:D013226	Status Epilepticus	muscle
HM03478	B4GALT4	esophagus	MESH:D002779	Cholestasis	liver
HM03478	B4GALT4	esophagus	MESH:D001778	Blood Coagulation Disorders	bone marrow
HM03478	B4GALT4	esophagus	MESH:D006943	Hyperglycemia
HM03478	B4GALT4	esophagus	MESH:D006529	Hepatomegaly
HM03478	B4GALT4	esophagus	MESH:D000550	Amblyopia	brain
HM03478	B4GALT4	esophagus	MESH:D000550	Amblyopia	brain
HM03478	B4GALT4	esophagus	MESH:D005315	Fetal Diseases
HM03478	B4GALT4	esophagus	MESH:D012640	Seizures	muscle
HM03478	B4GALT4	esophagus	MESH:D009203	Myocardial Infarction	heart
HM03478	B4GALT4	esophagus	MESH:D004830	Epilepsy, Tonic-Clonic	muscle
HM03478	B4GALT4	esophagus	MESH:D006333	Heart Failure	heart
HM03478	B4GALT4	esophagus	MESH:D009765	Obesity
HM03478	B4GALT4	esophagus	MESH:D014178	Translocation, Genetic
HM03478	B4GALT4	esophagus	MESH:D055371	Acute Lung Injury
HM03478	B4GALT4	esophagus	MESH:D001848	Bone Diseases, Developmental
HM03478	B4GALT4	esophagus	MESH:D008881	Migraine Disorders	brain
HM03478	B4GALT4	esophagus	MESH:D012559	Schizophrenia
HM03478	B4GALT4	esophagus	MESH:D009436	Neural Tube Defects
HM03478	B4GALT4	esophagus	MESH:D017029	Epilepsy, Complex Partial	muscle
HM03478	B4GALT4	esophagus	MESH:D004831	Epilepsies, Myoclonic	muscle
HM03478	B4GALT4	esophagus	MESH:D019247	HIV Wasting Syndrome
HM03478	B4GALT4	esophagus	MESH:D005234	Fatty Liver
HM03478	B4GALT4	esophagus	MESH:D016135	Spinal Dysraphism	spinal cord
HM03478	B4GALT4	esophagus	MESH:D014564	Urogenital Abnormalities
HM03478	B4GALT4	esophagus	MESH:D000015	Abnormalities, Multiple
HM03478	B4GALT4	esophagus	MESH:D001321	Autistic Disorder
HM03478	B4GALT4	esophagus	MESH:D009369	Neoplasms	spleen
HM03478	B4GALT4	esophagus	MESH:D009369	Neoplasms	bone marrow
HM03478	B4GALT4	esophagus	MESH:D004827	Epilepsy	muscle
HM03478	B4GALT4	esophagus	MESH:D012208	Rhabdomyosarcoma	rectum
HM03478	B4GALT4	esophagus	MESH:D012208	Rhabdomyosarcoma	prostate
HM03478	B4GALT4	esophagus	MESH:D012208	Rhabdomyosarcoma	muscle
HM03478	B4GALT4	esophagus	MESH:D006849	Hydrocephalus	brain
HM03478	B4GALT4	esophagus	MESH:D009139	Musculoskeletal Abnormalities
HM03478	B4GALT4	esophagus	MESH:D004828	Epilepsies, Partial	muscle
HM03478	B4GALT4	esophagus	MESH:D009135	Muscular Diseases	muscle
HM03478	B4GALT4	esophagus	MESH:D004487	Edema
HM03478	B4GALT4	esophagus	MESH:D005317	Fetal Growth Retardation
HM03478	B4GALT4	esophagus	MESH:D001714	Bipolar Disorder
HM03478	B4GALT4	esophagus	MESH:D003876	Dermatitis, Atopic	skin
HM03478	B4GALT4	esophagus	MESH:D008106	Liver Cirrhosis, Experimental
HM03478	B4GALT4	esophagus	MESH:D004421	Dystonia
HM03478	B4GALT4	esophagus	MESH:D019465	Craniofacial Abnormalities
HM03478	B4GALT4	esophagus	MESH:D056486	Drug-Induced Liver Injury