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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 |
|---|---|---|---|---|---|
| C0524851 | Neurodegenerative Disorders | HK1 | 3098 | hexokinase 1 | P19367 |
| C0524851 | Neurodegenerative Disorders | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0524851 | Neurodegenerative Disorders | INPPL1 | 3636 | inositol polyphosphate phosphatase like 1 | O15357 |
| C0524851 | Neurodegenerative Disorders | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
| C0524851 | Neurodegenerative Disorders | OGG1 | 4968 | 8-oxoguanine DNA glycosylase | O15527 |
| C0524851 | Neurodegenerative Disorders | ACO2 | 50 | aconitase 2 | Q99798 |
| C0524851 | Neurodegenerative Disorders | NAGPA | 51172 | N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase | Q9UK23 |
| C0524851 | Neurodegenerative Disorders | ADPRS | 54936 | ADP-ribosylserine hydrolase | Q9NX46 |
| C0524851 | Neurodegenerative Disorders | TIGAR | 57103 | TP53 induced glycolysis regulatory phosphatase | Q9NQ88 |
| C0524851 | Neurodegenerative Disorders | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0524851 | Neurodegenerative Disorders | MYORG | 57462 | myogenesis regulating glycosidase (putative) | Q6NSJ0 |
| C0524851 | Neurodegenerative Disorders | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0524851 | Neurodegenerative Disorders | L2HGDH | 79944 | L-2-hydroxyglutarate dehydrogenase | Q9H9P8 |
| C0524851 | Neurodegenerative Disorders | KL | 9365 | klotho | Q9UEF7 |
| C0524851 | Neurodegenerative Disorders | CD38 | 952 | CD38 molecule | P28907 |
| C0524851 | Neurodegenerative Disorders | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0524851 | Neurodegenerative Disorders | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
| C0524851 | Neurodegenerative Disorders | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
| C0524851 | Neurodegenerative Disorders | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0524851 | Neurodegenerative Disorders | CYP46A1 | 10858 | cytochrome P450 family 46 subfamily A member 1 | Q9Y6A2 |
| C0524851 | Neurodegenerative Disorders | CHGA | 1113 | chromogranin A | P10645 |
| C0524851 | Neurodegenerative Disorders | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0524851 | Neurodegenerative Disorders | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0524851 | Neurodegenerative Disorders | MGLL | 11343 | monoglyceride lipase | Q99685 |
| C0524851 | Neurodegenerative Disorders | VCAN | 1462 | versican | P13611 |
