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 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
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 |
C4540404 | SPINOCEREBELLAR ATAXIA 46 | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0002395 | Alzheimer's Disease | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0155143 | Acute follicular conjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0014493 | Epidemic keratoconjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0003873 | Rheumatoid Arthritis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0011615 | Dermatitis, Atopic | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0009763 | Conjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0002726 | Amyloidosis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0028738 | Nystagmus | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0036421 | Systemic Scleroderma | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0013595 | Eczema | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0034152 | Henoch-Schoenlein Purpura | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0036341 | Schizophrenia | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0009404 | Colorectal Neoplasms | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C1319315 | Adenocarcinoma of large intestine | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0005586 | Bipolar Disorder | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0037928 | Spinal Cord Diseases | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0005956 | Bone Marrow Diseases | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0004936 | Mental disorders | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0007102 | Malignant tumor of colon | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
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Last updated: August 19, 2024