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 48901 - 48925 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0426970 Spastic Quadriplegia COLGALT1 79709 collagen beta(1-O)galactosyltransferase 1 Q8NBJ5
C0013170 Drug habituation COLEC12 81035 collectin subfamily member 12 Q5KU26
C0026769 Multiple Sclerosis COLEC12 81035 collectin subfamily member 12 Q5KU26
C0013146 Drug abuse COLEC12 81035 collectin subfamily member 12 Q5KU26
C0524620 Metabolic Syndrome X COLEC12 81035 collectin subfamily member 12 Q5KU26
C0740858 Substance abuse problem COLEC12 81035 collectin subfamily member 12 Q5KU26
C0038580 Substance Dependence COLEC12 81035 collectin subfamily member 12 Q5KU26
C0026848 Myopathy COLEC12 81035 collectin subfamily member 12 Q5KU26
C0011860 Diabetes Mellitus, Non-Insulin-Dependent COLEC12 81035 collectin subfamily member 12 Q5KU26
C0038586 Substance Use Disorders COLEC12 81035 collectin subfamily member 12 Q5KU26
C0003850 Arteriosclerosis COLEC12 81035 collectin subfamily member 12 Q5KU26
C0013222 Drug Use Disorders COLEC12 81035 collectin subfamily member 12 Q5KU26
C0796279 Carnevale syndrome COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0032285 Pneumonia COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0008924 Cleft upper lip COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0038379 Strabismus COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0022283 Incontinentia Pigmenti Achromians COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0012739 Disseminated Intravascular Coagulation COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0036323 Schistosomiasis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C1704430 Urinary Schistosomiasis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0004623 Bacterial Infections COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0036439 Scoliosis, unspecified COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0008925 Cleft Palate COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0005744 Blepharophimosis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0022658 Kidney Diseases COLEC11 78989 collectin subfamily member 11 Q9BWP8

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Last updated: August 19, 2024