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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
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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:5082 | liver cirrhosis | HGNC:1854 | Homo sapiens (human) | 1060 | CENPC |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:10959 | Homo sapiens (human) | 10599 | SLCO1B1 |
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| DOID:13580 | cholestasis | HGNC:10959 | Homo sapiens (human) | 10599 | SLCO1B1 |
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| DOID:3571 | liver cancer | HGNC:10959 | Homo sapiens (human) | 10599 | SLCO1B1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:10283 | prostate cancer | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:0110403 | retinitis pigmentosa 13 | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:234 | colon adenocarcinoma | HGNC:14011 | Homo sapiens (human) | 10592 | SMC2 |
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| DOID:9256 | colorectal cancer | HGNC:14011 | Homo sapiens (human) | 10592 | SMC2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050453 | lissencephaly | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9884 | muscular dystrophy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9296 | cleft lip | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:3717 | gastric adenocarcinoma | MGI:2145995 | Mus musculus (house mouse) | 105827 | Amigo2 |
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| DOID:9970 | obesity | HGNC:14565 | Homo sapiens (human) | 10580 | SORBS1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:14565 | Homo sapiens (human) | 10580 | SORBS1 |
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| DOID:14330 | Parkinson's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:1612 | breast cancer | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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