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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▼ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0175697 | Van der Woude syndrome | UMOD | 7369 | uromodulin | P07911 |
C0175697 | Van der Woude syndrome | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0175697 | Van der Woude syndrome | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0175697 | Van der Woude syndrome | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0175697 | Van der Woude syndrome | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0175697 | Van der Woude syndrome | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
C0175697 | Van der Woude syndrome | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0175697 | Van der Woude syndrome | CNTN2 | 6900 | contactin 2 | Q02246 |
C0432272 | Van Buchem disease | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
C0042267 | Vaginitis | GLA | 2717 | galactosidase alpha | P06280 |
C0042258 | Vaginal Neoplasms | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0042258 | Vaginal Neoplasms | FH | 2271 | fumarate hydratase | P07954 |
C1631597 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) | THEM5 | 284486 | thioesterase superfamily member 5 | Q8N1Q8 |
C1631597 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) | CNTN3 | 5067 | contactin 3 | Q9P232 |
C1876172 | VAH, AUTOSOMAL RECESSIVE | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
C1848599 | VACTERL Association With Hydrocephalus | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C4554007 | Uveoretinal Coloboma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0042170 | Uveomeningoencephalitic Syndrome | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
C0042170 | Uveomeningoencephalitic Syndrome | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
C0042170 | Uveomeningoencephalitic Syndrome | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0042170 | Uveomeningoencephalitic Syndrome | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0042167 | Uveitis, Posterior | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0042167 | Uveitis, Posterior | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C0042166 | Uveitis, Intermediate | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0042164 | Uveitis | EXTL3 | 2137 | exostosin like glycosyltransferase 3 | O43909 |
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Last updated: August 19, 2024