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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
|---|---|---|---|---|---|
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0005684 | Malignant neoplasm of urinary bladder | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C1458155 | Mammary Neoplasms | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0155765 | Disease of capillaries | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0023895 | Liver diseases | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0006142 | Malignant neoplasm of breast | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0003850 | Arteriosclerosis | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0239946 | Fibrosis, Liver | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0013080 | Down Syndrome | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0008412 | Choline Deficiency | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C2239176 | Liver carcinoma | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0002395 | Alzheimer's Disease | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0004153 | Atherosclerosis | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0028754 | Obesity | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0005695 | Bladder Neoplasm | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0019880 | Homocystinuria | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0751202 | Cystathionine beta-Synthase Deficiency Disease | PEMT | 10400 | phosphatidylethanolamine N-methyltransferase | Q9UBM1 |
| C0019196 | Hepatitis C | PI4KB | 5298 | phosphatidylinositol 4-kinase beta | Q9UBF8 |
| C2748572 | SeSAME syndrome | PI4KB | 5298 | phosphatidylinositol 4-kinase beta | Q9UBF8 |
| C1175175 | Severe Acute Respiratory Syndrome | PI4KB | 5298 | phosphatidylinositol 4-kinase beta | Q9UBF8 |
| C2752007 | Congenital Disorder of Glycosylation, Type Io | DPM3 | 54344 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Q9P2X0 |
| C0016202 | Flatfoot | DPM3 | 54344 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Q9P2X0 |
| C0686353 | Muscular Dystrophies, Limb-Girdle | DPM3 | 54344 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Q9P2X0 |
| C0878544 | Cardiomyopathies | DPM3 | 54344 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Q9P2X0 |
