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 13176 - 13200 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0235974 Pancreatic carcinoma PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C0023418 leukemia PARG 8505 poly(ADP-ribose) glycohydrolase Q86W56
C0023418 leukemia PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C0346647 Malignant neoplasm of pancreas PARG 8505 poly(ADP-ribose) glycohydrolase Q86W56
C0346647 Malignant neoplasm of pancreas PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C0152013 Adenocarcinoma of lung (disorder) PARG 8505 poly(ADP-ribose) glycohydrolase Q86W56
C0152013 Adenocarcinoma of lung (disorder) PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C1458155 Mammary Neoplasms PARG 8505 poly(ADP-ribose) glycohydrolase Q86W56
C1458155 Mammary Neoplasms PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C1332986 Childhood Osteosarcoma PARG 8505 poly(ADP-ribose) glycohydrolase Q86W56
C1332986 Childhood Osteosarcoma PARG 8505 poly(ADP-ribose) glycohydrolase Q86WA6
C0699790 Colon Carcinoma PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C1458155 Mammary Neoplasms PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C0007102 Malignant tumor of colon PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C0006142 Malignant neoplasm of breast PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C0006826 Malignant Neoplasms PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C0017638 Glioma PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C1306459 Primary malignant neoplasm PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C0027651 Neoplasms PLEKHA8 84725 pleckstrin homology domain containing A8 Q96JA3
C1956346 Coronary Artery Disease PAFAH2 5051 platelet activating factor acetylhydrolase 2 Q99487
C0431375 Classical Lissencephaly PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034
C3714756 Intellectual Disability PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034
C3463824 MYELODYSPLASTIC SYNDROME PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034
C0266463 Lissencephaly PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034
C0265219 Miller Dieker syndrome PAFAH1B1 5048 platelet activating factor acetylhydrolase 1b regulatory subunit 1 P43034

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