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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 |
|---|---|---|---|---|---|
| C1335302 | Pancreatic Ductal Adenocarcinoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0026703 | Mucopolysaccharidoses | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0023269 | leiomyosarcoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0154830 | Proliferative diabetic retinopathy | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C1865322 | MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C1514428 | Primary peritoneal carcinoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0022661 | Kidney Failure, Chronic | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0009324 | Ulcerative Colitis | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0740394 | Hyperuricemia | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C1845076 | Lymphoproliferative Syndrome, X-Linked, 2 | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0235974 | Pancreatic carcinoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0031111 | Periostitis | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0020538 | Hypertensive disease | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0730278 | Severe nonproliferative diabetic retinopathy | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0242422 | Parkinsonian Disorders | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C0011989 | Camurati-Engelmann Syndrome | DPEP1 | 1800 | dipeptidase 1 | P16444 |
| C1847593 | EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850555 | De La Chapelle Dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0265274 | Achondrogenesis, type IB (disorder) | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1384666 | hearing impairment | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850554 | Atelosteogenesis type 2 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0220726 | Diastrophic dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029422 | Osteochondrodysplasias | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C3495559 | Juvenile arthritis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0025500 | Mesothelioma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
