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 5451 - 5475 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0024314 Lymphoproliferative Disorders SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0024419 Waldenstrom Macroglobulinemia SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0678222 Breast Carcinoma SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C1260326 Dendritic Cell Sarcoma, Interdigitating SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0028754 Obesity SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0024302 Reticulosarcoma SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0206641 Osteochondromatosis SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0152266 Mixed Cellularity Hodgkin Lymphoma SLC35B2 347734 solute carrier family 35 member B2 Q8TB61
C0027651 Neoplasms SLC35A4 113829 solute carrier family 35 member A4 Q96G79
C0026764 Multiple Myeloma SLC35A4 113829 solute carrier family 35 member A4 Q96G79
C0152013 Adenocarcinoma of lung (disorder) SLC35A4 113829 solute carrier family 35 member A4 Q96G79
C2239176 Liver carcinoma SLC35A4 113829 solute carrier family 35 member A4 Q96G79
C0006142 Malignant neoplasm of breast SLC35A4 113829 solute carrier family 35 member A4 Q96G79
C0265343 Jarcho-Levin syndrome SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0036572 Seizures SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0036439 Scoliosis, unspecified SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C3714756 Intellectual Disability SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0025958 Microcephaly SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0000768 Congenital Abnormality SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0085136 Central Nervous System Neoplasms SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0004352 Autistic Disorder SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0029422 Osteochondrodysplasias SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0282577 Congenital Disorders of Glycosylation SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C1510586 Autism Spectrum Disorders SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2
C0017638 Glioma SLC35A3 23443 solute carrier family 35 member A3 Q9Y2D2

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