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 49676 - 49700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0019829 Hodgkin Disease HABP4 22927 hyaluronan binding protein 4 Q5JVS0
C0848558 Hypospadias DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0520947 Clumsiness - motor delay DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0004930 Behavior Disorders DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0600139 Prostate carcinoma DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0016667 Fragile X Syndrome DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C2239176 Liver carcinoma DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0000768 Congenital Abnormality DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0010068 Coronary heart disease DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0036857 Severe intellectual disability DGKK 139189 diacylglycerol kinase kappa Q5KSL6
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
C0028754 Obesity SLC35D3 340146 solute carrier family 35 member D3 Q5M8T2
C0079504 Hermanski-Pudlak Syndrome SLC35D3 340146 solute carrier family 35 member D3 Q5M8T2
C0524620 Metabolic Syndrome X SLC35D3 340146 solute carrier family 35 member D3 Q5M8T2
C0242994 Hantavirus Infections SLC35D3 340146 solute carrier family 35 member D3 Q5M8T2

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Last updated: August 19, 2024