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 |
---|---|---|---|---|---|
C0205643 | Carcinoma, Cribriform | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0017152 | Gastritis | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0023467 | Leukemia, Myelocytic, Acute | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0042749 | Viremia | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0205641 | Adenocarcinoma, Basal Cell | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C1168401 | Squamous cell carcinoma of the head and neck | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0007131 | Non-Small Cell Lung Carcinoma | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C1333763 | Gastric Cardia Carcinoma | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0007222 | Cardiovascular Diseases | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0038356 | Stomach Neoplasms | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0020538 | Hypertensive disease | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0149931 | Migraine Disorders | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0013604 | Edema | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C1868672 | NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C3501848 | Nephrosis, congenital | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0235782 | Gallbladder Carcinoma | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0205645 | Adenocarcinoma, Tubular | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0005695 | Bladder Neoplasm | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C1708349 | Hereditary Diffuse Gastric Cancer | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0751688 | Malignant Squamous Cell Neoplasm | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0265219 | Miller Dieker syndrome | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0153452 | Malignant neoplasm of gallbladder | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0017154 | Gastritis, Atrophic | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0343641 | Human papilloma virus infection | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C3554460 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
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Last updated: August 19, 2024