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 1376 - 1400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0023470 Myeloid Leukemia SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0036572 Seizures SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0001418 Adenocarcinoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C3714581 Multicystic Dysplastic Kidney SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0279530 Malignant Bone Neoplasm SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0600139 Prostate carcinoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0041408 Turner Syndrome SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0009404 Colorectal Neoplasms SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0018818 Ventricular Septal Defects SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0242379 Malignant neoplasm of lung SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0037822 Speech Disorders SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1332979 Childhood Lymphoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1306459 Primary malignant neoplasm MGAT4B 11282 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B Q9UQ53
C1269683 Major Depressive Disorder MGAT4B 11282 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B Q9UQ53
C0006826 Malignant Neoplasms MGAT4B 11282 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B Q9UQ53
C0024141 Lupus Erythematosus, Systemic CNTN6 27255 contactin 6 Q9UQ52
C0010606 Adenoid Cystic Carcinoma CNTN6 27255 contactin 6 Q9UQ52
C0001973 Alcoholic Intoxication, Chronic CNTN6 27255 contactin 6 Q9UQ52
C0040517 Gilles de la Tourette syndrome CNTN6 27255 contactin 6 Q9UQ52
C3714756 Intellectual Disability CNTN6 27255 contactin 6 Q9UQ52
C0003125 Anorexia Nervosa CNTN6 27255 contactin 6 Q9UQ52
C0004352 Autistic Disorder CNTN6 27255 contactin 6 Q9UQ52
C1836230 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO CNTN6 27255 contactin 6 Q9UQ52
C1868675 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE CNTN6 27255 contactin 6 Q9UQ52
C4721610 Carcinoma, Ovarian Epithelial CNTN6 27255 contactin 6 Q9UQ52

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