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 61876 - 61900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0023418 leukemia SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C0086132 Depressive Symptoms SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C0011570 Mental Depression SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C0685938 Malignant neoplasm of gastrointestinal tract SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C0007131 Non-Small Cell Lung Carcinoma B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0027651 Neoplasms B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0006826 Malignant Neoplasms B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0007847 Malignant tumor of cervix B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0700095 Central neuroblastoma B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0021400 Influenza B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C1306459 Primary malignant neoplasm B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C4048328 cervical cancer B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0302592 Cervix carcinoma B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0027819 Neuroblastoma B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0343641 Human papilloma virus infection B3GNT3 10331 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Q9Y2A9
C0010964 Dandy-Walker Syndrome RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0266483 Pachygyria RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0029124 Optic Atrophy RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C3554381 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0265221 Walker-Warburg congenital muscular dystrophy RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C3714756 Intellectual Disability RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0017601 Glaucoma RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0266551 Congenital coloboma of iris RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0266544 Microcornea RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1
C0410174 Fukuyama Type Congenital Muscular Dystrophy RXYLT1 10329 ribitol xylosyltransferase 1 Q9Y2B1

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