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 9451 - 9475 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0006826 Malignant Neoplasms B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C3714756 Intellectual Disability B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0013384 Dyskinetic syndrome B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0751495 Seizures, Focal B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0029124 Optic Atrophy B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0010417 Cryptorchidism B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0037822 Speech Disorders B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0266483 Pachygyria B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0035305 Retinal Detachment B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0235946 Cerebral atrophy B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0266551 Congenital coloboma of iris B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0017601 Glaucoma B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0027651 Neoplasms B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0338502 Hypoplasia of the optic nerve B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C1261470 Congenital meningocele B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C1836373 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0410174 Fukuyama Type Congenital Muscular Dystrophy B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C1306459 Primary malignant neoplasm B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0684276 Hypsarrhythmia B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0038273 Stereotypic Movement Disorder B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0006142 Malignant neoplasm of breast B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C4284790 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0020255 Hydrocephalus B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0266544 Microcornea B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0011581 Depressive disorder B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0

About Release Notes Help Feedback

Click here to visit the beta site.


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