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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PLD1 | 5337 | phospholipase D1 | Q13393 |
C1561643 | Chronic Kidney Diseases | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0032285 | Pneumonia | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0002395 | Alzheimer's Disease | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0740392 | Infarction, Middle Cerebral Artery | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0014556 | Epilepsy, Temporal Lobe | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0013604 | Edema | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0030567 | Parkinson Disease | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0346037 | Acral Lentiginous Malignant Melanoma | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0024623 | Malignant neoplasm of stomach | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0021051 | Immunologic Deficiency Syndromes | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0040961 | Tricuspid Valve Insufficiency | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0029463 | Osteosarcoma | PLD1 | 5337 | phospholipase D1 | Q13393 |
C3714636 | Pneumonitis | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0600139 | Prostate carcinoma | PLD1 | 5337 | phospholipase D1 | Q13393 |
C0007102 | Malignant tumor of colon | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0699790 | Colon Carcinoma | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0003873 | Rheumatoid Arthritis | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0019158 | Hepatitis | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0036421 | Systemic Scleroderma | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0271097 | Usher Syndrome | PLD4 | 122618 | phospholipase D family member 4 | Q96BZ4 |
C0022573 | Keratoconjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0494463 | Alzheimer Disease, Late Onset | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0750901 | Alzheimer Disease, Early Onset | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
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Last updated: August 19, 2024