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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:0080828 | VEXAS syndrome | HGNC:12469 | Homo sapiens (human) | 7317 | UBA1 |
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| DOID:12365 | malaria | HGNC:4704 | Homo sapiens (human) | 2995 | GYPC |
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| DOID:0050887 | Townes-Brocks syndrome | HGNC:17748 | Homo sapiens (human) | 51339 | DACT1 |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112367 | Coffin-Siris syndrome 8 | HGNC:11105 | Homo sapiens (human) | 6601 | SMARCC2 |
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| DOID:0110662 | congenital myasthenic syndrome 1B | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0080611 | anterior segment dysgenesis 6 | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0050717 | methylmalonic aciduria and homocystinuria type cblF | HGNC:23038 | Homo sapiens (human) | 55788 | LMBRD1 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:2553 | Homo sapiens (human) | 8452 | CUL3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11924 | Homo sapiens (human) | 3604 | TNFRSF9 |
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| DOID:0111431 | essential tremor 4 | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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| DOID:14695 | galactokinase deficiency | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:10937 | Homo sapiens (human) | 6573 | SLC19A1 |
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| DOID:0080528 | bronchiectasis 3 | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:19194 | Homo sapiens (human) | 83872 | HMCN1 |
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| DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0112115 | combined oxidative phosphorylation deficiency 46 | HGNC:14509 | Homo sapiens (human) | 51649 | MRPS23 |
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| DOID:0111052 | Scott syndrome | HGNC:25240 | Homo sapiens (human) | 196527 | ANO6 |
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| DOID:0050978 | spinocerebellar ataxia type 29 | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0081318 | multiple synostoses syndrome 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:9256 | colorectal cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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