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 |
---|---|---|---|---|---|
C1861922 | CAMPOMELIC DYSPLASIA | LGALS4 | 3960 | galectin 4 | P56470 |
C1861922 | CAMPOMELIC DYSPLASIA | CHKB | 1120 | choline kinase beta | Q9Y259 |
C1861922 | CAMPOMELIC DYSPLASIA | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C1861922 | CAMPOMELIC DYSPLASIA | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C1861922 | CAMPOMELIC DYSPLASIA | CD177 | 57126 | CD177 molecule | Q8N6Q3 |
C1861922 | CAMPOMELIC DYSPLASIA | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C1862103 | Brachydactyly type C | MGAT3 | 4248 | beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase | Q09327 |
C1862103 | Brachydactyly type C | SI | 6476 | sucrase-isomaltase | P14410 |
C1862103 | Brachydactyly type C | MGAM | 8972 | maltase-glucoamylase | O43451 |
C1862112 | BRACHYDACTYLY, TYPE B1 | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | IDS | 3423 | iduronate 2-sulfatase | P22304 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | ENO2 | 2026 | enolase 2 | P09104 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | IGF2R | 3482 | insulin like growth factor 2 receptor | P11717 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | GAD1 | 2571 | glutamate decarboxylase 1 | Q99259 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | CAT | 847 | catalase | P04040 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | GPNMB | 10457 | glycoprotein nmb | Q14956 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C1862389 | ATRIAL SEPTAL DEFECT 1 | B3GLCT | 145173 | beta 3-glucosyltransferase | Q6Y288 |
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Last updated: August 19, 2024