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 4901 - 4925 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C0268547 Argininosuccinic Aciduria ARSA 410 arylsulfatase A P15289
C0268547 Argininosuccinic Aciduria RGN 9104 regucalcin Q15493
C0268547 Argininosuccinic Aciduria ARSD 414 arylsulfatase D P51689
C0078982 Arhinencephaly COMT 1312 catechol-O-methyltransferase P21964
C0078982 Arhinencephaly FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0078982 Arhinencephaly GAS1 2619 growth arrest specific 1 P54826
C0003803 Arnold Chiari Malformation SC5D 6309 sterol-C5-desaturase O75845
C0003803 Arnold Chiari Malformation PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0003803 Arnold Chiari Malformation PTEN 5728 phosphatase and tensin homolog P60484
C0349788 Arrhythmogenic Right Ventricular Dysplasia GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0349788 Arrhythmogenic Right Ventricular Dysplasia PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C0349788 Arrhythmogenic Right Ventricular Dysplasia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0349788 Arrhythmogenic Right Ventricular Dysplasia PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0349788 Arrhythmogenic Right Ventricular Dysplasia IL18R1 8809 interleukin 18 receptor 1 Q13478
C0349788 Arrhythmogenic Right Ventricular Dysplasia FASN 2194 fatty acid synthase P49327
C0349788 Arrhythmogenic Right Ventricular Dysplasia PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0349788 Arrhythmogenic Right Ventricular Dysplasia PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0003838 Arterial Occlusive Diseases IGF2R 3482 insulin like growth factor 2 receptor P11717
C0003838 Arterial Occlusive Diseases ICAM1 3383 intercellular adhesion molecule 1 P05362
C0003838 Arterial Occlusive Diseases STS 412 steroid sulfatase P08842
C0003838 Arterial Occlusive Diseases SELL 6402 selectin L P14151
C0003838 Arterial Occlusive Diseases EFNA5 1946 ephrin A5 P52803
C1859727 Arterial calcification of infancy ENPP1 5167 ectonucleotide pyrophosphatase/phosphodiesterase 1 P22413
C1859727 Arterial calcification of infancy NT5E 4907 5'-nucleotidase ecto P21589
C0852949 Arteriopathic disease ABO 28 ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase P16442

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