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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 |
|---|---|---|---|---|---|
| C0018802 | Congestive heart failure | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0018802 | Congestive heart failure | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0018802 | Congestive heart failure | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0009763 | Conjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
| C0009763 | Conjunctivitis | IMPA1 | 3612 | inositol monophosphatase 1 | P29218 |
| C0009763 | Conjunctivitis | LGALS1 | 3956 | galectin 1 | P09382 |
| C0009763 | Conjunctivitis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0009763 | Conjunctivitis | CD14 | 929 | CD14 molecule | P08571 |
| C1384514 | Conn Syndrome | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C1384514 | Conn Syndrome | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1384514 | Conn Syndrome | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1384514 | Conn Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C1384514 | Conn Syndrome | HSD3B2 | 3284 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | P26439 |
| C1384514 | Conn Syndrome | HSD3B1 | 3283 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 | P14060 |
| C1384514 | Conn Syndrome | LGALS3 | 3958 | galectin 3 | P17931 |
| C1384514 | Conn Syndrome | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1384514 | Conn Syndrome | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
| C1384514 | Conn Syndrome | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C1384514 | Conn Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C1384514 | Conn Syndrome | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
| C1384514 | Conn Syndrome | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
| C0009782 | Connective Tissue Diseases | B3GALT6 | 126792 | beta-1,3-galactosyltransferase 6 | Q96L58 |
| C0009782 | Connective Tissue Diseases | B4GALT7 | 11285 | beta-1,4-galactosyltransferase 7 | Q9UBV7 |
| C0009782 | Connective Tissue Diseases | GLB1 | 2720 | galactosidase beta 1 | P16278 |
| C0009782 | Connective Tissue Diseases | PLOD3 | 8985 | procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 | O60568 |
