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 42851 - 42875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0016978 gallbladder neoplasm CNTN4 152330 contactin 4 Q8IWV2
C0005586 Bipolar Disorder CNTN4 152330 contactin 4 Q8IWV2
C0004936 Mental disorders CNTN4 152330 contactin 4 Q8IWV2
C4721610 Carcinoma, Ovarian Epithelial CNTN4 152330 contactin 4 Q8IWV2
C0153452 Malignant neoplasm of gallbladder CNTN4 152330 contactin 4 Q8IWV2
C3714756 Intellectual Disability CNTN4 152330 contactin 4 Q8IWV2
C0028754 Obesity CNTN4 152330 contactin 4 Q8IWV2
C0036572 Seizures CNTN4 152330 contactin 4 Q8IWV2
C1140680 Malignant neoplasm of ovary CNTN4 152330 contactin 4 Q8IWV2
C0009402 Colorectal Carcinoma CNTN4 152330 contactin 4 Q8IWV2
C1510586 Autism Spectrum Disorders CNTN4 152330 contactin 4 Q8IWV2
C0031511 Pheochromocytoma CNTN4 152330 contactin 4 Q8IWV2
C0024117 Chronic Obstructive Airway Disease CNTN4 152330 contactin 4 Q8IWV2
C0919267 ovarian neoplasm CNTN4 152330 contactin 4 Q8IWV2
C1857276 Trichohepatoenteric Syndrome CNTN4 152330 contactin 4 Q8IWV2
C0020538 Hypertensive disease CNTN4 152330 contactin 4 Q8IWV2
C0339573 Glaucoma, Primary Open Angle CNTN4 152330 contactin 4 Q8IWV2
C1862941 Amyotrophic Lateral Sclerosis, Sporadic CNTN4 152330 contactin 4 Q8IWV2
C4014261 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 CNTN4 152330 contactin 4 Q8IWV2
C1833798 Optic Nerve Aplasia, Bilateral CNTN4 152330 contactin 4 Q8IWV2
C0678222 Breast Carcinoma CNTN3 5067 contactin 3 Q9P232
C0037926 Compression of spinal cord CNTN3 5067 contactin 3 Q9P232
C0162871 Aortic Aneurysm, Abdominal CNTN3 5067 contactin 3 Q9P232
C0524620 Metabolic Syndrome X CNTN3 5067 contactin 3 Q9P232
C0265224 Freeman-Sheldon syndrome CNTN3 5067 contactin 3 Q9P232

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Last updated: August 19, 2024