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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:0111420 | familial GPIHBP1 deficiency | MGI:1915703 | Mus musculus (house mouse) | 68453 | Gpihbp1 |
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| DOID:14735 | hereditary angioedema | RGD:1584381 | Rattus norvegicus (Norway rat) | 684979 | Hs3st6 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1121 | Homo sapiens (human) | 685 | BTC |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1121 | Homo sapiens (human) | 685 | BTC |
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| DOID:3892 | insulinoma | HGNC:1121 | Homo sapiens (human) | 685 | BTC |
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| DOID:10754 | otitis media | HGNC:1121 | Homo sapiens (human) | 685 | BTC |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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| DOID:612 | primary immunodeficiency disease | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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| DOID:0112332 | pontocerebellar hypoplasia type 13 | MGI:1915755 | Mus musculus (house mouse) | 68505 | Vps51 |
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| DOID:0070346 | neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies | MGI:1915760 | Mus musculus (house mouse) | 68510 | Ints1 |
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| DOID:83 | cataract | MGI:1915760 | Mus musculus (house mouse) | 68510 | Ints1 |
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| DOID:11723 | Duchenne muscular dystrophy | MGI:1915769 | Mus musculus (house mouse) | 68519 | Eml1 |
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| DOID:2490 | congenital nervous system abnormality | MGI:1915769 | Mus musculus (house mouse) | 68519 | Eml1 |
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| DOID:0111169 | subcortical band heterotopia | MGI:1915769 | Mus musculus (house mouse) | 68519 | Eml1 |
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| DOID:0111571 | Weyers acrofacial dysostosis | MGI:1915775 | Mus musculus (house mouse) | 68525 | Evc2 |
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| DOID:12714 | Ellis-Van Creveld syndrome | MGI:1915775 | Mus musculus (house mouse) | 68525 | Evc2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:1470 | major depressive disorder | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0112122 | X-linked epilepsy with variable learning disabilities and behavior disorders | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0112029 | non-syndromic X-linked intellectual disability 50 | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:1826 | epilepsy | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:5419 | schizophrenia | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:0112035 | non-syndromic X-linked intellectual disability 96 | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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| DOID:1574 | alcohol use disorder | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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