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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 |
|---|---|---|---|---|---|
| C0020179 | Huntington Disease | GYS1 | 2997 | glycogen synthase 1 | P13807 |
| C0020179 | Huntington Disease | IDH1 | 3417 | isocitrate dehydrogenase (NADP(+)) 1 | O75874 |
| C0020179 | Huntington Disease | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
| C0020179 | Huntington Disease | OGG1 | 4968 | 8-oxoguanine DNA glycosylase | O15527 |
| C0020179 | Huntington Disease | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
| C0020179 | Huntington Disease | PC | 5091 | pyruvate carboxylase | P11498 |
| C0020179 | Huntington Disease | ACO2 | 50 | aconitase 2 | Q99798 |
| C0020179 | Huntington Disease | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
| C0020179 | Huntington Disease | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C0020179 | Huntington Disease | GBA2 | 57704 | glucosylceramidase beta 2 | Q9HCG7 |
| C0020179 | Huntington Disease | KL | 9365 | klotho | Q9UEF7 |
| C0020179 | Huntington Disease | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
| C0020179 | Huntington Disease | CYP46A1 | 10858 | cytochrome P450 family 46 subfamily A member 1 | Q9Y6A2 |
| C0020179 | Huntington Disease | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0020179 | Huntington Disease | MGLL | 11343 | monoglyceride lipase | Q99685 |
| C0020179 | Huntington Disease | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0020179 | Huntington Disease | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0020179 | Huntington Disease | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
| C0020179 | Huntington Disease | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0020179 | Huntington Disease | ALPP | 250 | alkaline phosphatase, placental | P05187 |
| C0020179 | Huntington Disease | ALPI | 248 | alkaline phosphatase, intestinal | P09923 |
| C0020179 | Huntington Disease | IPMK | 253430 | inositol polyphosphate multikinase | Q8NFU5 |
| C0020179 | Huntington Disease | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0020179 | Huntington Disease | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0020179 | Huntington Disease | SIGLEC7 | 27036 | sialic acid binding Ig like lectin 7 | Q9Y286 |
