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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
C0026769 | Multiple Sclerosis | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0025500 | Mesothelioma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0862312 | Epithelioid mesothelioma, malignant | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0011615 | Dermatitis, Atopic | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0010068 | Coronary heart disease | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0029458 | Osteoporosis, Postmenopausal | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C1956346 | Coronary Artery Disease | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0011849 | Diabetes Mellitus | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0007097 | Carcinoma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0033860 | Psoriasis | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0151744 | Myocardial Ischemia | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0001418 | Adenocarcinoma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
C0024623 | Malignant neoplasm of stomach | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0206657 | Alveolar Soft Part Sarcoma | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0242379 | Malignant neoplasm of lung | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0279544 | Adult Alveolar Soft Part Sarcoma | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0279985 | Childhood Alveolar Soft Part Sarcoma | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C2239176 | Liver carcinoma | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0009402 | Colorectal Carcinoma | TMED6 | 146456 | transmembrane p24 trafficking protein 6 | Q8WW62 |
C0037773 | Spastic Paraplegia, Hereditary | FAR1 | 84188 | fatty acyl-CoA reductase 1 | Q8WVX9 |
C0025958 | Microcephaly | FAR1 | 84188 | fatty acyl-CoA reductase 1 | Q8WVX9 |
C0282529 | Chondrodysplasia Punctata, Rhizomelic | FAR1 | 84188 | fatty acyl-CoA reductase 1 | Q8WVX9 |
C0013595 | Eczema | FAR1 | 84188 | fatty acyl-CoA reductase 1 | Q8WVX9 |
C2749283 | Gm2-Gangliosidosis, Variant B1 | HEXD | 284004 | hexosaminidase D | Q8WVB3 |
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Last updated: August 19, 2024