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 39526 - 39550 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0017168 Gastroesophageal reflux disease NT5E 4907 5'-nucleotidase ecto P21589
C0028738 Nystagmus NT5E 4907 5'-nucleotidase ecto P21589
C1848745 Oliver-McFarlane syndrome NT5E 4907 5'-nucleotidase ecto P21589
C2981150 Uranostaphyloschisis NT5E 4907 5'-nucleotidase ecto P21589
C1260873 Aortic valve disorder NT5E 4907 5'-nucleotidase ecto P21589
C0280324 Laryngeal Squamous Cell Carcinoma NT5E 4907 5'-nucleotidase ecto P21589
C0279651 Gallbladder adenocarcinoma NT5E 4907 5'-nucleotidase ecto P21589
C0085409 Polyendocrinopathies, Autoimmune NT5E 4907 5'-nucleotidase ecto P21589
C0003467 Anxiety NT5E 4907 5'-nucleotidase ecto P21589
C0750974 Brain Tumor, Primary NT5E 4907 5'-nucleotidase ecto P21589
C0085110 Severe Combined Immunodeficiency NT5E 4907 5'-nucleotidase ecto P21589
C0007103 Malignant neoplasm of endometrium NT5E 4907 5'-nucleotidase ecto P21589
C1859726 ARTERIAL TORTUOSITY SYNDROME NT5E 4907 5'-nucleotidase ecto P21589
C0017152 Gastritis NT5E 4907 5'-nucleotidase ecto P21589
C0020179 Huntington Disease NT5E 4907 5'-nucleotidase ecto P21589
C2242813 Ranula (disorder) NT5E 4907 5'-nucleotidase ecto P21589
C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency NT5E 4907 5'-nucleotidase ecto P21589
C0031099 Periodontitis NT5E 4907 5'-nucleotidase ecto P21589
C0013080 Down Syndrome NT5E 4907 5'-nucleotidase ecto P21589
C0014544 Epilepsy NT5E 4907 5'-nucleotidase ecto P21589
C0024959 Maxillary Sinusitis NT5E 4907 5'-nucleotidase ecto P21589
C0026703 Mucopolysaccharidoses NT5E 4907 5'-nucleotidase ecto P21589
C0010054 Coronary Arteriosclerosis NT5E 4907 5'-nucleotidase ecto P21589
C0024904 Mastoiditis NT5E 4907 5'-nucleotidase ecto P21589
C0795864 Smith-Magenis syndrome NT5M 56953 5',3'-nucleotidase, mitochondrial Q9NPB1

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