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 50301 - 50325 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0015695 Fatty Liver CHKA 1119 choline kinase alpha P35790
C0699743 Congenital muscular dystrophy (disorder) CHKA 1119 choline kinase alpha P35790
C0235974 Pancreatic carcinoma CHKA 1119 choline kinase alpha P35790
C0080178 Spina Bifida CHKA 1119 choline kinase alpha P35790
C0919267 ovarian neoplasm CHKA 1119 choline kinase alpha P35790
C0027819 Neuroblastoma CHKA 1119 choline kinase alpha P35790
C0033578 Prostatic Neoplasms CHKA 1119 choline kinase alpha P35790
C1865233 Muscular Dystrophy, Congenital, Megaconial Type CHKA 1119 choline kinase alpha P35790
C0279626 Squamous cell carcinoma of esophagus CHKA 1119 choline kinase alpha P35790
C0030297 Pancreatic Neoplasm CHKA 1119 choline kinase alpha P35790
C1335302 Pancreatic Ductal Adenocarcinoma CHKA 1119 choline kinase alpha P35790
C0009375 Colonic Neoplasms CHKA 1119 choline kinase alpha P35790
C0266508 Rachischisis CHKA 1119 choline kinase alpha P35790
C0002066 Alkaptonuria CHIT1 1118 chitinase 1 Q13231
C0003850 Arteriosclerosis CHIT1 1118 chitinase 1 Q13231
C0028064 Niemann-Pick Diseases CHIT1 1118 chitinase 1 Q13231
C1961835 Gaucher Disease, Type 1 CHIT1 1118 chitinase 1 Q13231
C0264408 Childhood asthma CHIT1 1118 chitinase 1 Q13231
C0002736 Amyotrophic Lateral Sclerosis CHIT1 1118 chitinase 1 Q13231
C0220756 Niemann-Pick Disease, Type C CHIT1 1118 chitinase 1 Q13231
C0085131 Gangliosidosis GM1 CHIT1 1118 chitinase 1 Q13231
C0017205 Gaucher Disease CHIT1 1118 chitinase 1 Q13231
C0004096 Asthma CHIT1 1118 chitinase 1 Q13231
C0041296 Tuberculosis CHIT1 1118 chitinase 1 Q13231
C0151744 Myocardial Ischemia CHIT1 1118 chitinase 1 Q13231

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Last updated: August 19, 2024