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 |
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C1257965 | Compensatory Hyperinsulinemia | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C1257965 | Compensatory Hyperinsulinemia | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
C1258085 | Barrett Epithelium | AKR1B10 | 57016 | aldo-keto reductase family 1 member B10 | O60218 |
C1258085 | Barrett Epithelium | AKR1C2 | 1646 | aldo-keto reductase family 1 member C2 | P52895 |
C1258085 | Barrett Epithelium | CDH13 | 1012 | cadherin 13 | P55290 |
C1258085 | Barrett Epithelium | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C1258104 | Diffuse Scleroderma | HEXA | 3073 | hexosaminidase subunit alpha | P06865 |
C1258104 | Diffuse Scleroderma | CAT | 847 | catalase | P04040 |
C1258104 | Diffuse Scleroderma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C1260325 | Dendritic Cell Sarcoma, Follicular | FCER2 | 2208 | Fc fragment of IgE receptor II | P06734 |
C1260326 | Dendritic Cell Sarcoma, Interdigitating | SLC35B2 | 347734 | solute carrier family 35 member B2 | Q8TB61 |
C1260386 | Glucocorticoid-remediable aldosteronism | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
C1260386 | Glucocorticoid-remediable aldosteronism | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
C1260386 | Glucocorticoid-remediable aldosteronism | ISYNA1 | 51477 | inositol-3-phosphate synthase 1 | Q9NPH2 |
C1260386 | Glucocorticoid-remediable aldosteronism | CAT | 847 | catalase | P04040 |
C1260386 | Glucocorticoid-remediable aldosteronism | CBR1 | 873 | carbonyl reductase 1 | P16152 |
C1260386 | Glucocorticoid-remediable aldosteronism | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1260386 | Glucocorticoid-remediable aldosteronism | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
C1260386 | Glucocorticoid-remediable aldosteronism | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C1260386 | Glucocorticoid-remediable aldosteronism | GML | 2765 | glycosylphosphatidylinositol anchored molecule like | Q99445 |
C1260396 | Alpha thalassemia intermedia | PC | 5091 | pyruvate carboxylase | P11498 |
C1260402 | Splenic sequestration | SCD | 6319 | stearoyl-CoA desaturase | O00767 |
C1260873 | Aortic valve disorder | ENPP1 | 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 | P22413 |
C1260873 | Aortic valve disorder | KL | 9365 | klotho | Q9UEF7 |
C1260873 | Aortic valve disorder | ACAN | 176 | aggrecan | P16112 |
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Last updated: August 19, 2024