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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 |
|---|---|---|---|---|---|
| C0042900 | Vitiligo | CAT | 847 | catalase | P04040 |
| C0042900 | Vitiligo | CBR1 | 873 | carbonyl reductase 1 | P16152 |
| C0042900 | Vitiligo | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0042900 | Vitiligo | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
| C0042900 | Vitiligo | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0042900 | Vitiligo | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0042900 | Vitiligo | PARP12 | 64761 | poly(ADP-ribose) polymerase family member 12 | Q9H0J9 |
| C0042900 | Vitiligo | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
| C0042900 | Vitiligo | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0042900 | Vitiligo | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0042900 | Vitiligo | PLCB3 | 5331 | phospholipase C beta 3 | Q01970 |
| C0042900 | Vitiligo | PRNP | 5621 | prion protein | F7VJQ1 |
| C0042900 | Vitiligo | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0042900 | Vitiligo | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0019562 | Von Hippel-Lindau Syndrome | TUSC3 | 7991 | tumor suppressor candidate 3 | Q13454 |
| C0019562 | Von Hippel-Lindau Syndrome | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0019562 | Von Hippel-Lindau Syndrome | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
| C0019562 | Von Hippel-Lindau Syndrome | CHGA | 1113 | chromogranin A | P10645 |
| C0019562 | Von Hippel-Lindau Syndrome | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
| C0019562 | Von Hippel-Lindau Syndrome | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0019562 | Von Hippel-Lindau Syndrome | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0019562 | Von Hippel-Lindau Syndrome | SDHC | 6391 | succinate dehydrogenase complex subunit C | Q99643 |
| C0019562 | Von Hippel-Lindau Syndrome | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
| C0019562 | Von Hippel-Lindau Syndrome | IDH2 | 3418 | isocitrate dehydrogenase (NADP(+)) 2 | P48735 |
| C0019562 | Von Hippel-Lindau Syndrome | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
