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:0110527 | autosomal recessive nonsyndromic deafness 8 | HGNC:11877 | Homo sapiens (human) | 64699 | TMPRSS3 |
|
||
| DOID:0080592 | Klippel-Feil syndrome 4 | HGNC:18150 | Homo sapiens (human) | 84700 | MYO18B |
|
||
| DOID:0110013 | advanced sleep phase syndrome 3 | HGNC:8847 | Homo sapiens (human) | 8863 | PER3 |
|
||
| DOID:0111594 | distal arthrogryposis type 5D | HGNC:3147 | Homo sapiens (human) | 9427 | ECEL1 |
|
||
| DOID:0110068 | frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
|
||
| DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
|
||
| DOID:0111899 | X-linked thrombophilia due to factor IX defect | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
|
||
| DOID:0111381 | IVIC syndrome | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
|
||
| DOID:0080244 | Galloway-Mowat syndrome 2 | HGNC:26058 | Homo sapiens (human) | 8270 | LAGE3 |
|
||
| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
|
||
| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
|
||
| DOID:0070122 | Meckel syndrome 8 | HGNC:25774 | Homo sapiens (human) | 79867 | TCTN2 |
|
||
| DOID:4586 | familial meningioma | HGNC:8800 | Homo sapiens (human) | 5155 | PDGFB |
|
||
| DOID:0111062 | familial hypobetalipoproteinemia 1 | HGNC:603 | Homo sapiens (human) | 338 | APOB |
|
||
| DOID:10825 | essential hypertension | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
|
||
| DOID:0080950 | alopecia-mental retardation syndrome 4 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
|
||
| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0080030 | spondyloepimetaphyseal dysplasia, Missouri type | HGNC:7159 | Homo sapiens (human) | 4322 | MMP13 |
|
||
| DOID:0110158 | Charcot-Marie-Tooth disease type 2I | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
|
||
| DOID:0110028 | age related macular degeneration 5 | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
|
||
| DOID:3526 | cerebral infarction | HGNC:9403 | Homo sapiens (human) | 5583 | PRKCH |
|
||
| DOID:0081122 | Catel Manzke syndrome | HGNC:20324 | Homo sapiens (human) | 23483 | TGDS |
|
||
| DOID:0111927 | spermatogenic failure 37 | HGNC:30761 | Homo sapiens (human) | 199223 | TTC21A |
|
||
| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
|
||
| DOID:0110035 | Alzheimer's disease 2 | HGNC:613 | Homo sapiens (human) | 348 | APOE |
|
