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 |
---|---|---|---|---|---|
C1269683 | Major Depressive Disorder | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0017668 | Focal glomerulosclerosis | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0023521 | Globoid cell leukodystrophy | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0026769 | Multiple Sclerosis | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0036202 | Sarcoidosis | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0004623 | Bacterial Infections | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0004364 | Autoimmune Diseases | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0282488 | Interstitial Cystitis | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0033578 | Prostatic Neoplasms | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0852036 | Pregnancy associated hypertension | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C0017661 | IGA Glomerulonephritis | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C1510586 | Autism Spectrum Disorders | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0011847 | Diabetes | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0006826 | Malignant Neoplasms | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C1861305 | TARSAL-CARPAL COALITION SYNDROME | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C1269683 | Major Depressive Disorder | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0007138 | Carcinoma, Transitional Cell | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0027651 | Neoplasms | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0007137 | Squamous cell carcinoma | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C0007131 | Non-Small Cell Lung Carcinoma | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
C0235480 | Paroxysmal atrial fibrillation | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
C0028754 | Obesity | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
C0152013 | Adenocarcinoma of lung (disorder) | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
C0004238 | Atrial Fibrillation | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
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