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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 |
|---|---|---|---|---|---|
| C1449563 | Cardiomyopathy, Familial Idiopathic | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0334634 | Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0024314 | Lymphoproliferative Disorders | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0024419 | Waldenstrom Macroglobulinemia | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0678222 | Breast Carcinoma | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C1260326 | Dendritic Cell Sarcoma, Interdigitating | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0028754 | Obesity | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0024302 | Reticulosarcoma | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0206641 | Osteochondromatosis | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0152266 | Mixed Cellularity Hodgkin Lymphoma | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC35B3 | 51000 | solute carrier family 35 member B3 | Q9H1N7 |
| C0376358 | Malignant neoplasm of prostate | SLC35B4 | 84912 | solute carrier family 35 member B4 | Q969S0 |
| C0024623 | Malignant neoplasm of stomach | SLC35B4 | 84912 | solute carrier family 35 member B4 | Q969S0 |
| C0699791 | Stomach Carcinoma | SLC35B4 | 84912 | solute carrier family 35 member B4 | Q969S0 |
| C0600139 | Prostate carcinoma | SLC35B4 | 84912 | solute carrier family 35 member B4 | Q969S0 |
| C0398739 | Congenital disorder of glycosylation, type 2C | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0003467 | Anxiety | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0025958 | Microcephaly | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0013336 | Dwarfism | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0007642 | Cellulitis | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0013528 | Echolalia | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C2239176 | Liver carcinoma | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0029422 | Osteochondrodysplasias | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0024236 | Lymphedema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0008925 | Cleft Palate | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
