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 62476 - 62500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0018818 Ventricular Septal Defects GPC6 10082 glypican 6 Q9Y625
C1306459 Primary malignant neoplasm GPC6 10082 glypican 6 Q9Y625
C0010278 Craniosynostosis GPC6 10082 glypican 6 Q9Y625
C0027651 Neoplasms GPC6 10082 glypican 6 Q9Y625
C0751406 Post-Traumatic Osteoporosis GPC6 10082 glypican 6 Q9Y625
C0242383 Age related macular degeneration HS3ST4 9951 heparan sulfate-glucosamine 3-sulfotransferase 4 Q9Y661
C1961102 Precursor Cell Lymphoblastic Leukemia Lymphoma HS3ST4 9951 heparan sulfate-glucosamine 3-sulfotransferase 4 Q9Y661
C0236733 Amphetamine-Related Disorders HS3ST4 9951 heparan sulfate-glucosamine 3-sulfotransferase 4 Q9Y661
C0269102 Endometrioma HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0007131 Non-Small Cell Lung Carcinoma HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0005695 Bladder Neoplasm HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0006142 Malignant neoplasm of breast HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0019163 Hepatitis B HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0235974 Pancreatic carcinoma HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0005684 Malignant neoplasm of urinary bladder HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0014175 Endometriosis HS3ST3B1 9953 heparan sulfate-glucosamine 3-sulfotransferase 3B1 Q9Y662
C0006142 Malignant neoplasm of breast HS3ST3A1 9955 heparan sulfate-glucosamine 3-sulfotransferase 3A1 Q9Y663
C0678222 Breast Carcinoma HS3ST3A1 9955 heparan sulfate-glucosamine 3-sulfotransferase 3A1 Q9Y663
C2930997 Congenital disorder of glycosylation type 1C ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0282577 Congenital Disorders of Glycosylation ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0349653 Congenital disorder of glycosylation type 1A ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0038379 Strabismus ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0014544 Epilepsy ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0036572 Seizures ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672
C0272375 Antithrombin III Deficiency ALG6 29929 ALG6 alpha-1,3-glucosyltransferase Q9Y672

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Last updated: August 19, 2024