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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 |
|---|---|---|---|---|---|
| C0686347 | Tardive Dyskinesia | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
| C0686347 | Tardive Dyskinesia | PIP4K2C | 79837 | phosphatidylinositol-5-phosphate 4-kinase type 2 gamma | Q8TBX8 |
| C0686347 | Tardive Dyskinesia | HSPG2 | 3339 | heparan sulfate proteoglycan 2 | P98160 |
| C0686347 | Tardive Dyskinesia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0686347 | Tardive Dyskinesia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0686347 | Tardive Dyskinesia | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
| C0686347 | Tardive Dyskinesia | PIP4K2A | 5305 | phosphatidylinositol-5-phosphate 4-kinase type 2 alpha | P48426 |
| C0949664 | Tauopathies | OGT | 8473 | O-linked N-acetylglucosamine (GlcNAc) transferase | O15294 |
| C0949664 | Tauopathies | OGA | 10724 | O-GlcNAcase | O60502 |
| C0949664 | Tauopathies | CHI3L1 | 1116 | chitinase 3 like 1 | P36222 |
| C0949664 | Tauopathies | CYP46A1 | 10858 | cytochrome P450 family 46 subfamily A member 1 | Q9Y6A2 |
| C0949664 | Tauopathies | GGT1 | 2678 | gamma-glutamyltransferase 1 | P19440 |
| C0949664 | Tauopathies | INPP5K | 51763 | inositol polyphosphate-5-phosphatase K | Q9BT40 |
| C0949664 | Tauopathies | PRNP | 5621 | prion protein | P04156 |
| C0949664 | Tauopathies | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
| C0949664 | Tauopathies | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
| C0949664 | Tauopathies | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C0949664 | Tauopathies | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
| C0949664 | Tauopathies | PRNP | 5621 | prion protein | F7VJQ1 |
| C0949664 | Tauopathies | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0949664 | Tauopathies | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C1956413 | Taussig-Bing Anomaly | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0039373 | Tay-Sachs Disease | GBA | 2629 | glucosylceramidase beta | P04062 |
| C0039373 | Tay-Sachs Disease | GM2A | 2760 | GM2 ganglioside activator | P17900 |
| C0039373 | Tay-Sachs Disease | HEXA | 3073 | hexosaminidase subunit alpha | P06865 |
