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 |
---|---|---|---|---|---|
C0037822 | Speech Disorders | PAFAH1B1 | 5048 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | P43034 |
C0037822 | Speech Disorders | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0037789 | Specific reading disorder | ARSD | 414 | arylsulfatase D | P51689 |
C2931356 | Spastic paraplegia type 5A, recessive | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
C2931356 | Spastic paraplegia type 5A, recessive | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C1858712 | Spastic paraplegia 10, autosomal dominant | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C1858712 | Spastic paraplegia 10, autosomal dominant | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0338596 | Spastic cerebral palsy | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
C0338596 | Spastic cerebral palsy | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0426970 | Spastic Quadriplegia | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
C0426970 | Spastic Quadriplegia | GLB1 | 2720 | galactosidase beta 1 | P16278 |
C0426970 | Spastic Quadriplegia | ARSA | 410 | arylsulfatase A | P15289 |
C0426970 | Spastic Quadriplegia | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0426970 | Spastic Quadriplegia | CYB5R3 | 1727 | cytochrome b5 reductase 3 | P00387 |
C0426970 | Spastic Quadriplegia | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
C0426970 | Spastic Quadriplegia | GAD1 | 2571 | glutamate decarboxylase 1 | Q99259 |
C0426970 | Spastic Quadriplegia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0426970 | Spastic Quadriplegia | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
C0426970 | Spastic Quadriplegia | PDHX | 8050 | pyruvate dehydrogenase complex component X | O00330 |
C0426970 | Spastic Quadriplegia | DEGS1 | 8560 | delta 4-desaturase, sphingolipid 1 | O15121 |
C0426970 | Spastic Quadriplegia | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
C0426970 | Spastic Quadriplegia | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0037773 | Spastic Paraplegia, Hereditary | B4GALNT1 | 2583 | beta-1,4-N-acetyl-galactosaminyltransferase 1 | Q00973 |
C0037773 | Spastic Paraplegia, Hereditary | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
C0037773 | Spastic Paraplegia, Hereditary | GBA2 | 57704 | glucosylceramidase beta 2 | Q9HCG7 |
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