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 |
---|---|---|---|---|---|
C0549473 | Thyroid carcinoma | KL | 9365 | klotho | Q9UEF7 |
C4721610 | Carcinoma, Ovarian Epithelial | KL | 9365 | klotho | Q9UEF7 |
C0220701 | RETINITIS PIGMENTOSA 1 | KL | 9365 | klotho | Q9UEF7 |
C0035579 | Rickets | KL | 9365 | klotho | Q9UEF7 |
C0085215 | Ovarian Failure, Premature | KL | 9365 | klotho | Q9UEF7 |
C0085682 | Hypophosphatemia | KL | 9365 | klotho | Q9UEF7 |
C0178664 | Glomerulosclerosis (disorder) | KL | 9365 | klotho | Q9UEF7 |
C0948008 | Ischemic stroke | KL | 9365 | klotho | Q9UEF7 |
C0699885 | Carcinoma of bladder | KL | 9365 | klotho | Q9UEF7 |
C0079744 | Diffuse Large B-Cell Lymphoma | KL | 9365 | klotho | Q9UEF7 |
C0010068 | Coronary heart disease | KL | 9365 | klotho | Q9UEF7 |
C0036341 | Schizophrenia | KL | 9365 | klotho | Q9UEF7 |
C1876187 | TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL | KL | 9365 | klotho | Q9UEF7 |
C0037274 | Dermatologic disorders | KL | 9365 | klotho | Q9UEF7 |
C0242231 | Coronary Stenosis | KL | 9365 | klotho | Q9UEF7 |
C0001787 | Osteoporosis, Age-Related | KL | 9365 | klotho | Q9UEF7 |
C1956346 | Coronary Artery Disease | KL | 9365 | klotho | Q9UEF7 |
C0346647 | Malignant neoplasm of pancreas | KL | 9365 | klotho | Q9UEF7 |
C0007134 | Renal Cell Carcinoma | KL | 9365 | klotho | Q9UEF7 |
C0524851 | Neurodegenerative Disorders | KL | 9365 | klotho | Q9UEF7 |
C1269683 | Major Depressive Disorder | KL | 9365 | klotho | Q9UEF7 |
C0520679 | Sleep Apnea, Obstructive | KL | 9365 | klotho | Q9UEF7 |
C0007115 | Malignant neoplasm of thyroid | KL | 9365 | klotho | Q9UEF7 |
C0678222 | Breast Carcinoma | KL | 9365 | klotho | Q9UEF7 |
C1134719 | Invasive Ductal Breast Carcinoma | KL | 9365 | klotho | Q9UEF7 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024