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 58151 - 58175 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0007137 Squamous cell carcinoma CNTN1 1272 contactin 1 Q12860
C0442874 Neuropathy CNTN1 1272 contactin 1 Q12860
C0546837 Malignant neoplasm of esophagus CNTN1 1272 contactin 1 Q12860
C0684249 Carcinoma of lung CNTN1 1272 contactin 1 Q12860
C0024623 Malignant neoplasm of stomach CNTN1 1272 contactin 1 Q12860
C0009402 Colorectal Carcinoma CNTN1 1272 contactin 1 Q12860
C0699791 Stomach Carcinoma CNTN1 1272 contactin 1 Q12860
C1276035 Pena-Shokeir syndrome type I CNTN1 1272 contactin 1 Q12860
C0014859 Esophageal Neoplasms CNTN1 1272 contactin 1 Q12860
C0600139 Prostate carcinoma CNTN1 1272 contactin 1 Q12860
C0027726 Nephrotic Syndrome CNTN1 1272 contactin 1 Q12860
C0152018 Esophageal carcinoma CNTN1 1272 contactin 1 Q12860
C0030567 Parkinson Disease CNTN1 1272 contactin 1 Q12860
C0376358 Malignant neoplasm of prostate CNTN1 1272 contactin 1 Q12860
C0279626 Squamous cell carcinoma of esophagus CNTN1 1272 contactin 1 Q12860
C1263846 Attention deficit hyperactivity disorder CNTN1 1272 contactin 1 Q12860
C0003864 Arthritis CNTN1 1272 contactin 1 Q12860
C0265534 Scaphycephaly CNTN1 1272 contactin 1 Q12860
C0002395 Alzheimer's Disease CNTN1 1272 contactin 1 Q12860
C0149925 Small cell carcinoma of lung CNTN1 1272 contactin 1 Q12860
C0017665 Membranous glomerulonephritis CNTN1 1272 contactin 1 Q12860
C0270960 Congenital myopathy (disorder) CNTN1 1272 contactin 1 Q12860
C0018378 Guillain-Barre Syndrome CNTN1 1272 contactin 1 Q12860
C0017638 Glioma CNTN1 1272 contactin 1 Q12860
C0020224 Polyhydramnios CNTN1 1272 contactin 1 Q12860

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Last updated: August 19, 2024