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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 ▼ |
|---|---|---|---|---|---|
| C0030297 | Pancreatic Neoplasm | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C1319315 | Adenocarcinoma of large intestine | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0220668 | Congenital contractural arachnodactyly | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C1332206 | Adult Lymphoma | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0020538 | Hypertensive disease | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0024530 | Malaria | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0302592 | Cervix carcinoma | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C4721532 | Lymphoma, Non-Hodgkin, Familial | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0014548 | Epilepsy, Generalized | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0700095 | Central neuroblastoma | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0015695 | Fatty Liver | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0024301 | Lymphoma, Follicular | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C1332979 | Childhood Lymphoma | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0175697 | Van der Woude syndrome | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0162531 | Hereditary Coproporphyria | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0002395 | Alzheimer's Disease | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0342859 | Harderoporphyria | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0009402 | Colorectal Carcinoma | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C3149631 | MELORHEOSTOSIS, ISOLATED | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C1321551 | Shprintzen-Goldberg syndrome | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0494463 | Alzheimer Disease, Late Onset | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0012236 | DiGeorge Syndrome | CPO | 130749 | carboxypeptidase O | Q8IVL8 |
| C0010346 | Crohn Disease | LACC1 | 144811 | laccase domain containing 1 | Q8IV20 |
| C0009324 | Ulcerative Colitis | LACC1 | 144811 | laccase domain containing 1 | Q8IV20 |
| C3495559 | Juvenile arthritis | LACC1 | 144811 | laccase domain containing 1 | Q8IV20 |
