DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 57551 - 57575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1332201 Adult Diffuse Large B-Cell Lymphoma CD109 135228 CD109 molecule Q6YHK3
C0410174 Fukuyama Type Congenital Muscular Dystrophy CD109 135228 CD109 molecule Q6YHK3
C0555198 Malignant Glioma CD109 135228 CD109 molecule Q6YHK3
C0026848 Myopathy CD109 135228 CD109 molecule Q6YHK3
C0600139 Prostate carcinoma CD109 135228 CD109 molecule Q6YHK3
C0003873 Rheumatoid Arthritis CD109 135228 CD109 molecule Q6YHK3
C0376358 Malignant neoplasm of prostate CD109 135228 CD109 molecule Q6YHK3
C0205944 Sarcoma, Epithelioid CD109 135228 CD109 molecule Q6YHK3
C1176475 Ductal Carcinoma CD109 135228 CD109 molecule Q6YHK3
C0036341 Schizophrenia B3GAT2 135152 beta-1,3-glucuronyltransferase 2 Q9NPZ5
C0004763 Barrett Esophagus B3GAT2 135152 beta-1,3-glucuronyltransferase 2 Q9NPZ5
C1861172 Venous Thromboembolism B3GAT2 135152 beta-1,3-glucuronyltransferase 2 Q9NPZ5
C0023903 Liver neoplasms ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C2239176 Liver carcinoma ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C0024620 Primary Malignant Liver Neoplasm ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C0345904 Malignant neoplasm of liver ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C1858991 Childhood Ataxia with Central Nervous System Hypomyelinization ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C0023520 Leukodystrophy ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C0854795 Resectable Malignant Liver Neoplasm ACOT12 134526 acyl-CoA thioesterase 12 Q8WYK0
C0028754 Obesity GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7
C0524620 Metabolic Syndrome X GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7
C0020538 Hypertensive disease GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7
C0030567 Parkinson Disease GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7
C0007222 Cardiovascular Diseases GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7
C3179455 Niemann-Pick Disease, Type C1 GNPDA2 132789 glucosamine-6-phosphate deaminase 2 Q8TDQ7

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Last updated: August 19, 2024