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:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
|
||
| DOID:0050477 | Liddle syndrome | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
|
||
| DOID:0110169 | Charcot-Marie-Tooth disease axonal type 2P | HGNC:25135 | Homo sapiens (human) | 90678 | LRSAM1 |
|
||
| DOID:0090060 | Wolcott-Rallison syndrome | HGNC:3255 | Homo sapiens (human) | 9451 | EIF2AK3 |
|
||
| DOID:0090034 | myoclonic dystonia 11 | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
|
||
| DOID:0090107 | autosomal dominant hypocalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
|
||
| DOID:0111555 | Alkuraya-Kucinskas syndrome | HGNC:26953 | Homo sapiens (human) | 84162 | BLTP1 |
|
||
| DOID:0050475 | Weill-Marchesani syndrome | HGNC:13201 | Homo sapiens (human) | 81794 | ADAMTS10 |
|
||
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
|
||
| DOID:10584 | retinitis pigmentosa | HGNC:30859 | Homo sapiens (human) | 23020 | SNRNP200 |
|
||
| DOID:14687 | diastrophic dysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
|
||
| DOID:0060581 | Noonan syndrome 3 | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
|
||
| DOID:0060705 | X-linked lymphoproliferative syndrome 1 | HGNC:10820 | Homo sapiens (human) | 4068 | SH2D1A |
|
||
| DOID:0110083 | arrhythmogenic right ventricular dysplasia 12 | HGNC:6207 | Homo sapiens (human) | 3728 | JUP |
|
||
| DOID:0080697 | Opitz GBBB syndrome | HGNC:7095 | Homo sapiens (human) | 4281 | MID1 |
|
||
| DOID:783 | end stage renal disease | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
|
||
| DOID:3911 | progeria | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
|
||
| DOID:0111100 | maturity-onset diabetes of the young type 2 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
|
||
| DOID:0111395 | mucopolysaccharidosis type IIIA | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
|
||
| DOID:9452 | steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
|
||
| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
|
||
| DOID:14766 | renal agenesis | HGNC:31042 | Homo sapiens (human) | 80000 | GREB1L |
|
||
| DOID:0111248 | cerebrocostomandibular syndrome | HGNC:11153 | Homo sapiens (human) | 6628 | SNRPB |
|
