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 ▲ |
---|---|---|---|---|---|
C0302592 | Cervix carcinoma | KL | 9365 | klotho | Q9UEF7 |
C0035086 | Renal Osteodystrophy | KL | 9365 | klotho | Q9UEF7 |
C0029607 | Other emphysema | KL | 9365 | klotho | Q9UEF7 |
C0041696 | Unipolar Depression | KL | 9365 | klotho | Q9UEF7 |
C0021670 | insulinoma | KL | 9365 | klotho | Q9UEF7 |
C0338831 | Manic | KL | 9365 | klotho | Q9UEF7 |
C3160718 | PARKINSON DISEASE, LATE-ONSET | KL | 9365 | klotho | Q9UEF7 |
C0003850 | Arteriosclerosis | KL | 9365 | klotho | Q9UEF7 |
C0525045 | Mood Disorders | KL | 9365 | klotho | Q9UEF7 |
C0036421 | Systemic Scleroderma | KL | 9365 | klotho | Q9UEF7 |
C0038454 | Cerebrovascular accident | KL | 9365 | klotho | Q9UEF7 |
C0156259 | Hypertrophy of kidney | KL | 9365 | klotho | Q9UEF7 |
C1449563 | Cardiomyopathy, Familial Idiopathic | KL | 9365 | klotho | Q9UEF7 |
C0085681 | Hyperphosphatemia (disorder) | KL | 9365 | klotho | Q9UEF7 |
C0006826 | Malignant Neoplasms | KL | 9365 | klotho | Q9UEF7 |
C0242379 | Malignant neoplasm of lung | KL | 9365 | klotho | Q9UEF7 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | KL | 9365 | klotho | Q9UEF7 |
C1800706 | Idiopathic Pulmonary Fibrosis | KL | 9365 | klotho | Q9UEF7 |
C0005684 | Malignant neoplasm of urinary bladder | KL | 9365 | klotho | Q9UEF7 |
C0027721 | Lipoid nephrosis | KL | 9365 | klotho | Q9UEF7 |
C0020502 | Hyperparathyroidism | KL | 9365 | klotho | Q9UEF7 |
C0205824 | Liposarcoma, Dedifferentiated | KL | 9365 | klotho | Q9UEF7 |
C0549473 | Thyroid carcinoma | KL | 9365 | klotho | Q9UEF7 |
C4721610 | Carcinoma, Ovarian Epithelial | KL | 9365 | klotho | Q9UEF7 |
C0220701 | RETINITIS PIGMENTOSA 1 | KL | 9365 | klotho | Q9UEF7 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024