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 426 - 450 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0040580 Tracheal Diseases UGT2A1 10941 UDP glucuronosyltransferase family 2 member A1 complex locus Q9Y4X1
C0677886 Epithelial ovarian cancer UGT2A1 10941 UDP glucuronosyltransferase family 2 member A1 complex locus Q9Y4X1
C0006826 Malignant Neoplasms UGT2A1 10941 UDP glucuronosyltransferase family 2 member A1 complex locus Q9Y4X1
C4721610 Carcinoma, Ovarian Epithelial UGT2A1 10941 UDP glucuronosyltransferase family 2 member A1 complex locus Q9Y4X1
C0677886 Epithelial ovarian cancer UGT2A2 574537 UDP glucuronosyltransferase family 2 member A2 Q9Y4X1
C4721610 Carcinoma, Ovarian Epithelial UGT2A2 574537 UDP glucuronosyltransferase family 2 member A2 Q9Y4X1
C0025202 melanoma CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0376358 Malignant neoplasm of prostate CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0600139 Prostate carcinoma CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0004096 Asthma CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0027651 Neoplasms CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0013274 Patent ductus arteriosus CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0026764 Multiple Myeloma CRYBG1 202 crystallin beta-gamma domain containing 1 Q9Y4K1
C0009324 Ulcerative Colitis CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C0029463 Osteosarcoma CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C1850900 Familial primary gastric lymphoma CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C0002736 Amyotrophic Lateral Sclerosis CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C0585442 Osteosarcoma of bone CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C0027651 Neoplasms CHST2 9435 carbohydrate sulfotransferase 2 Q9Y4C5
C0010495 Cutis Laxa ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0027092 Myopia ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C4479409 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0852949 Arteriopathic disease ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0007766 Intracranial Aneurysm ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C1318518 Infantile malignant osteopetrosis ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487

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Last updated: August 19, 2024