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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 |
|---|---|---|---|---|---|
| C0014544 | Epilepsy | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0600139 | Prostate carcinoma | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C1333762 | Gastric Cardia Adenocarcinoma | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0018798 | Congenital Heart Defects | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0079741 | Lymphoma, Intermediate-Grade | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0699885 | Carcinoma of bladder | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0024304 | Lymphoma, Mixed-Cell | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C1561643 | Chronic Kidney Diseases | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0038454 | Cerebrovascular accident | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0238463 | Papillary thyroid carcinoma | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0279626 | Squamous cell carcinoma of esophagus | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0027765 | nervous system disorder | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0019158 | Hepatitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0006840 | Candidiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0018889 | Helminthiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0024117 | Chronic Obstructive Airway Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0700345 | Candidiasis, Vulvovaginal | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1394891 | Intrinsic Factor Deficiency | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0022568 | Keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0026946 | Mycoses | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0041296 | Tuberculosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1262117 | Fungal keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0037299 | Skin Ulcer | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0345904 | Malignant neoplasm of liver | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0235974 | Pancreatic carcinoma | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
