Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:0050554 | X-linked sideroblastic anemia with ataxia | HGNC:48 | Homo sapiens (human) | 22 | ABCB7 |
|
||
| DOID:9245 | Alagille syndrome | MGI:1095416 | Mus musculus (house mouse) | 16449 | Jag1 |
|
||
| DOID:576 | proteinuria | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
|
||
| DOID:10652 | Alzheimer's disease | MGI:88059 | Mus musculus (house mouse) | 11820 | App |
|
||
| DOID:14323 | Marfan syndrome | MGI:95489 | Mus musculus (house mouse) | 14118 | Fbn1 |
|
||
| DOID:3883 | Lynch syndrome | MGI:101938 | Mus musculus (house mouse) | 17350 | Mlh1 |
|
||
| DOID:2741 | bilirubin metabolic disorder | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
|
||
| DOID:0060601 | alpha-2-plasmin inhibitor deficiency | MGI:107173 | Mus musculus (house mouse) | 18816 | Serpinf2 |
|
||
| DOID:2217 | Bernard-Soulier syndrome | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
|
||
| DOID:0060439 | lysinuric protein intolerance | HGNC:11065 | Homo sapiens (human) | 9056 | SLC7A7 |
|
||
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
|
||
| DOID:1588 | thrombocytopenia | HGNC:7217 | Homo sapiens (human) | 4352 | MPL |
|
||
| DOID:13481 | thanatophoric dysplasia | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
|
||
| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
|
||
| DOID:12308 | Dubin-Johnson syndrome | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
|
||
| DOID:13994 | cleidocranial dysplasia | MGI:99829 | Mus musculus (house mouse) | 12393 | Runx2 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:613 | Homo sapiens (human) | 348 | APOE |
|
||
| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
|
||
| DOID:0090140 | cortisone reductase deficiency 2 | MGI:103562 | Mus musculus (house mouse) | 15483 | Hsd11b1 |
|
||
| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:99255 | Mus musculus (house mouse) | 14103 | Fasl |
|
||
| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas |
|
||
| DOID:9074 | systemic lupus erythematosus | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas |
|
||
| DOID:0110867 | congenital stationary night blindness 1C | MGI:1330305 | Mus musculus (house mouse) | 17364 | Trpm1 |
|
||
| DOID:0050545 | visceral heterotaxy | MGI:106676 | Mus musculus (house mouse) | 22773 | Zic3 |
|
||
| DOID:0110918 | hereditary spherocytosis type 3 | MGI:98385 | Mus musculus (house mouse) | 20739 | Spta1 |
|
