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 51826 - 51850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0020476 Hyperlipoproteinemias GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0003850 Arteriosclerosis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0010054 Coronary Arteriosclerosis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0001339 Acute pancreatitis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0011849 Diabetes Mellitus GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0007222 Cardiovascular Diseases GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0020473 Hyperlipidemia GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0025517 Metabolic Diseases GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0011847 Diabetes GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0004153 Atherosclerosis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0017638 Glioma GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0030305 Pancreatitis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0267937 Acute recurrent pancreatitis GPIHBP1 338328 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 Q8IV16
C0010346 Crohn Disease LACC1 144811 laccase domain containing 1 Q8IV20
C0009324 Ulcerative Colitis LACC1 144811 laccase domain containing 1 Q8IV20
C3495559 Juvenile arthritis LACC1 144811 laccase domain containing 1 Q8IV20
C0031046 Pericarditis LACC1 144811 laccase domain containing 1 Q8IV20
C0003864 Arthritis LACC1 144811 laccase domain containing 1 Q8IV20
C0021390 Inflammatory Bowel Diseases LACC1 144811 laccase domain containing 1 Q8IV20
C0015230 Exanthema LACC1 144811 laccase domain containing 1 Q8IV20
C0042165 Anterior uveitis LACC1 144811 laccase domain containing 1 Q8IV20
C0175697 Van der Woude syndrome CPO 130749 carboxypeptidase O Q8IVL8
C0162531 Hereditary Coproporphyria CPO 130749 carboxypeptidase O Q8IVL8
C0002395 Alzheimer's Disease CPO 130749 carboxypeptidase O Q8IVL8
C0342859 Harderoporphyria CPO 130749 carboxypeptidase O Q8IVL8

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Last updated: August 19, 2024