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 |
---|---|---|---|---|---|
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 |
C0011847 | Diabetes | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0028754 | Obesity | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0007103 | Malignant neoplasm of endometrium | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0011127 | Pressure Ulcer | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C1306459 | Primary malignant neoplasm | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0476089 | Endometrial Carcinoma | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0742343 | Acute Chest Syndrome | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0003869 | Arthritis, Infectious | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0011849 | Diabetes Mellitus | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0520679 | Sleep Apnea, Obstructive | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0002395 | Alzheimer's Disease | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024