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:0070529 | Sifrim-Hitz-Weiss syndrome | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
|
||
| DOID:0110428 | dilated cardiomyopathy 1AA | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
|
||
| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
|
||
| DOID:0111353 | arthrogryposis, renal dysfunction, and cholestasis 1 | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
|
||
| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
|
||
| DOID:0080980 | arthrogryposis multiplex congenita-4 | HGNC:19286 | Homo sapiens (human) | 55681 | SCYL2 |
|
||
| DOID:0111637 | autosomal recessive nonsyndromic deafness 112 | HGNC:13652 | Homo sapiens (human) | 55814 | BDP1 |
|
||
| DOID:0111620 | corneal dystrophy-perceptive deafness syndrome | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
|
||
| DOID:0111853 | primary ciliary dyskinesia 40 | HGNC:2953 | Homo sapiens (human) | 1770 | DNAH9 |
|
||
| DOID:0110176 | Charcot-Marie-Tooth disease axonal type 2X | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
|
||
| DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
|
||
| DOID:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
|
||
| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
|
||
| DOID:0050778 | Meckel syndrome | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
|
||
| DOID:0070067 | White-Sutton syndrome | HGNC:18801 | Homo sapiens (human) | 23126 | POGZ |
|
||
| DOID:0081156 | common variable immunodeficiency 14 | HGNC:21729 | Homo sapiens (human) | 359948 | IRF2BP2 |
|
||
| DOID:0080253 | Meckel syndrome 13 | HGNC:28128 | Homo sapiens (human) | 84314 | TMEM107 |
|
||
| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
| DOID:0080953 | amelogenesis imperfecta type 1J | HGNC:14376 | Homo sapiens (human) | 93650 | ACP4 |
|
||
| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
|
||
| DOID:0080694 | Galloway-Mowat syndrome | HGNC:28905 | Homo sapiens (human) | 79693 | YRDC |
|
||
| DOID:0080517 | Meier-Gorlin syndrome 6 | HGNC:17493 | Homo sapiens (human) | 51053 | GMNN |
|
||
| DOID:0070096 | oculocutaneous albinism type II | HGNC:6929 | Homo sapiens (human) | 4157 | MC1R |
|
||
| DOID:0081135 | agammaglobulinemia 2 | HGNC:5870 | Homo sapiens (human) | 3543 | IGLL1 |
|
||
| DOID:0110187 | Charcot-Marie-Tooth disease type 4K | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
|
