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 276 - 300 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0025202 melanoma GPC6 10082 glypican 6 Q9Y625
C4510897 Omodysplasia GPC6 10082 glypican 6 Q9Y625
C0007222 Cardiovascular Diseases GPC6 10082 glypican 6 Q9Y625
C0006826 Malignant Neoplasms GPC6 10082 glypican 6 Q9Y625
C0029459 Osteoporosis, Senile GPC6 10082 glypican 6 Q9Y625
C1306503 Congenital exomphalos GPC6 10082 glypican 6 Q9Y625
C1263846 Attention deficit hyperactivity disorder GPC6 10082 glypican 6 Q9Y625
C0796154 SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 GPC6 10082 glypican 6 Q9Y625
C0035335 Retinoblastoma GPC6 10082 glypican 6 Q9Y625
C0027932 Neurotic Disorders GPC6 10082 glypican 6 Q9Y625
C0009402 Colorectal Carcinoma GPC6 10082 glypican 6 Q9Y625
C0018916 Hemangioma GPC6 10082 glypican 6 Q9Y625
C0006142 Malignant neoplasm of breast GPC6 10082 glypican 6 Q9Y625
C4721610 Carcinoma, Ovarian Epithelial GPC6 10082 glypican 6 Q9Y625
C0010417 Cryptorchidism GPC6 10082 glypican 6 Q9Y625
C0033999 Pterygium GPC6 10082 glypican 6 Q9Y625
C0001787 Osteoporosis, Age-Related GPC6 10082 glypican 6 Q9Y625
C0751484 Sporadic Retinoblastoma GPC6 10082 glypican 6 Q9Y625
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
C0796012 Krause-Kivlin syndrome B3GALT1 8708 beta-1,3-galactosyltransferase 1 Q9Y5Z6
C0001418 Adenocarcinoma B3GALT1 8708 beta-1,3-galactosyltransferase 1 Q9Y5Z6

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Last updated: August 19, 2024