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
Displaying entries 60776 - 60800 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C0042170 Uveomeningoencephalitic Syndrome CLEC16A 23274 C-type lectin domain containing 16A Q2KHT3
C4554007 Uveoretinal Coloboma ALDH7A1 501 aldehyde dehydrogenase 7 family member A1 P49419
C1848599 VACTERL Association With Hydrocephalus PTEN 5728 phosphatase and tensin homolog P60484
C1876172 VAH, AUTOSOMAL RECESSIVE CFC1 55997 cripto, FRL-1, cryptic family 1 P0CG37
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
C0042258 Vaginal Neoplasms SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0042258 Vaginal Neoplasms FH 2271 fumarate hydratase P07954
C0042267 Vaginitis GLA 2717 galactosidase alpha P06280
C0432272 Van Buchem disease CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0175697 Van der Woude syndrome PKM 5315 pyruvate kinase M1/2 P14618
C0175697 Van der Woude syndrome CPO 130749 carboxypeptidase O Q8IVL8
C0175697 Van der Woude syndrome PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
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
C0042341 Varicocele OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0042341 Varicocele MGLL 11343 monoglyceride lipase Q99685
C0042341 Varicocele HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0042341 Varicocele LYPD5 284348 LY6/PLAUR domain containing 5 Q6UWN5

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024