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:0050465 | Muir-Torre syndrome | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
|
||
| DOID:612 | primary immunodeficiency disease | HGNC:1706 | Homo sapiens (human) | 925 | CD8A |
|
||
| DOID:0050983 | spinocerebellar ataxia type 36 | HGNC:15911 | Homo sapiens (human) | 10528 | NOP56 |
|
||
| DOID:3209 | junctional epidermolysis bullosa | HGNC:6139 | Homo sapiens (human) | 3675 | ITGA3 |
|
||
| DOID:0050637 | Finnish type amyloidosis | HGNC:4620 | Homo sapiens (human) | 2934 | GSN |
|
||
| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
|
||
| DOID:0060241 | 3-M syndrome | HGNC:21024 | Homo sapiens (human) | 9820 | CUL7 |
|
||
| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
|
||
| DOID:0080585 | Van Maldergem syndrome 1 | HGNC:13681 | Homo sapiens (human) | 8642 | DCHS1 |
|
||
| DOID:0070072 | autosomal dominant intellectual developmental disorder 42 | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
|
||
| DOID:0081152 | common variable immunodeficiency 10 | HGNC:7795 | Homo sapiens (human) | 4791 | NFKB2 |
|
||
| DOID:9410 | panhypopituitarism | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
|
||
| DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
|
||
| DOID:0110315 | hypertrophic cardiomyopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0080261 | autosomal recessive nonsyndromic deafness 106 | HGNC:21296 | Homo sapiens (human) | 64787 | EPS8L2 |
|
||
| DOID:0111958 | immunodeficiency 11B | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
|
||
| DOID:0070145 | hereditary sensory and autonomic neuropathy type 5 | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
|
||
| DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
|
||
| DOID:11105 | fundus albipunctatus | HGNC:9940 | Homo sapiens (human) | 5959 | RDH5 |
|
||
| DOID:0070138 | autosomal recessive cutis laxa type IIIB | HGNC:9721 | Homo sapiens (human) | 5831 | PYCR1 |
|
||
| DOID:0081212 | autosomal recessive intellectual developmental disorder 48 | HGNC:31399 | Homo sapiens (human) | 388662 | SLC6A17 |
|
||
| DOID:0080944 | familial Behcet-like autoinflammatory syndrome | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
|
||
| DOID:0111144 | preterm premature rupture of the membranes | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
|
||
| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
|
||
| DOID:0060197 | amyotrophic lateral sclerosis type 5 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
|
