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 43276 - 43300 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0524620 Metabolic Syndrome X CNTN2 6900 contactin 2 Q02246
C0017636 Glioblastoma CNTN2 6900 contactin 2 Q02246
C0037928 Spinal Cord Diseases CNTN2 6900 contactin 2 Q02246
C0024299 Lymphoma CNTN2 6900 contactin 2 Q02246
C0242287 Isaacs syndrome CNTN2 6900 contactin 2 Q02246
C0555198 Malignant Glioma CNTN2 6900 contactin 2 Q02246
C0036572 Seizures CNTN2 6900 contactin 2 Q02246
C0030567 Parkinson Disease CNTN2 6900 contactin 2 Q02246
C0280475 Childhood Oligodendroglioma CNTN2 6900 contactin 2 Q02246
C0024314 Lymphoproliferative Disorders CNTN2 6900 contactin 2 Q02246
C0003864 Arthritis CNTN2 6900 contactin 2 Q02246
C0149925 Small cell carcinoma of lung CNTN2 6900 contactin 2 Q02246
C0079773 Lymphoma, T-Cell, Cutaneous CNTN2 6900 contactin 2 Q02246
C0027830 neurofibroma CNTN2 6900 contactin 2 Q02246
C0007131 Non-Small Cell Lung Carcinoma CNTN2 6900 contactin 2 Q02246
C0027831 Neurofibromatosis 1 CNTN2 6900 contactin 2 Q02246
C1332979 Childhood Lymphoma CNTN2 6900 contactin 2 Q02246
C0004114 Astrocytoma CNTN2 6900 contactin 2 Q02246
C0494475 Tonic - clonic seizures CNTN2 6900 contactin 2 Q02246
C0014544 Epilepsy CNTN2 6900 contactin 2 Q02246
C0279070 Adult Oligodendroglioma CNTN2 6900 contactin 2 Q02246
C0151744 Myocardial Ischemia ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0025958 Microcephaly ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0086543 Cataract ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0013421 Dystonia ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252

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Last updated: August 19, 2024