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 13651 - 13675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0038356 Stomach Neoplasms PLPP1 8611 phospholipid phosphatase 1 O14494
C0024623 Malignant neoplasm of stomach PLPP1 8611 phospholipid phosphatase 1 O14494
C3714636 Pneumonitis PLD2 5338 phospholipase D2 O14939
C0009402 Colorectal Carcinoma PLD2 5338 phospholipase D2 O14939
C0009319 Colitis PLD2 5338 phospholipase D2 O14939
C1261473 Sarcoma PLD2 5338 phospholipase D2 O14939
C0007102 Malignant tumor of colon PLD2 5338 phospholipase D2 O14939
C0030567 Parkinson Disease PLD2 5338 phospholipase D2 O14939
C1458155 Mammary Neoplasms PLD2 5338 phospholipase D2 O14939
C0006826 Malignant Neoplasms PLD2 5338 phospholipase D2 O14939
C0600139 Prostate carcinoma PLD2 5338 phospholipase D2 O14939
C0024299 Lymphoma PLD2 5338 phospholipase D2 O14939
C0006142 Malignant neoplasm of breast PLD2 5338 phospholipase D2 O14939
C0699790 Colon Carcinoma PLD2 5338 phospholipase D2 O14939
C0027651 Neoplasms PLD2 5338 phospholipase D2 O14939
C0004114 Astrocytoma PLD2 5338 phospholipase D2 O14939
C0678222 Breast Carcinoma PLD2 5338 phospholipase D2 O14939
C0338106 Adenocarcinoma of colon PLD2 5338 phospholipase D2 O14939
C0233794 Memory impairment PLD2 5338 phospholipase D2 O14939
C0238463 Papillary thyroid carcinoma PLD2 5338 phospholipase D2 O14939
C0024141 Lupus Erythematosus, Systemic PLD2 5338 phospholipase D2 O14939
C4722524 Blood Vessel Tumors PLD2 5338 phospholipase D2 O14939
C0007134 Renal Cell Carcinoma PLD2 5338 phospholipase D2 O14939
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma PLD2 5338 phospholipase D2 O14939
C1306459 Primary malignant neoplasm PLD2 5338 phospholipase D2 O14939

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Last updated: August 19, 2024