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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 / OrganismsTools
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Glycan Converters
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GALAXY
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Guidelines
MIRAGE
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 | January 28, 2025 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3320 | Tay-Sachs disease | MGI:96073 | Mus musculus (house mouse) | 15211 | Hexa | author statement supported by traceable reference |
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| DOID:12930 | dilated cardiomyopathy | MGI:106658 | Mus musculus (house mouse) | 20807 | Srf | author statement supported by traceable reference |
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| DOID:0060850 | annular pancreas | MGI:96533 | Mus musculus (house mouse) | 16147 | Ihh | author statement supported by traceable reference |
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| DOID:0050651 | atrioventricular septal defect | MGI:1100864 | Mus musculus (house mouse) | 13411 | Dnah11 | author statement supported by traceable reference |
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| DOID:4184 | pseudohypoparathyroidism | MGI:95777 | Mus musculus (house mouse) | 14683 | Gnas | author statement supported by traceable reference |
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| DOID:1572 | normal pressure hydrocephalus | MGI:2444131 | Mus musculus (house mouse) | 231293 | Cwh43 | author statement supported by traceable reference |
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| DOID:8893 | psoriasis | MGI:108074 | Mus musculus (house mouse) | 20773 | Sptlc2 | author statement supported by traceable reference |
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| DOID:10754 | otitis media | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna | author statement supported by traceable reference |
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| DOID:0090142 | cystathioninuria | MGI:1339968 | Mus musculus (house mouse) | 107869 | Cth | author statement supported by traceable reference |
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| DOID:0110423 | dilated cardiomyopathy 1C | MGI:1344412 | Mus musculus (house mouse) | 24131 | Ldb3 | author statement supported by traceable reference |
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| DOID:0060877 | bullous congenital ichthyosiform erythroderma | MGI:96699 | Mus musculus (house mouse) | 16681 | Krt2 | author statement supported by traceable reference |
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| DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | MGI:1096317 | Mus musculus (house mouse) | 13628 | Eef1a2 | author statement supported by traceable reference |
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| DOID:14330 | Parkinson's disease | MGI:1342774 | Mus musculus (house mouse) | 19017 | Ppargc1a | author statement supported by traceable reference |
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| DOID:0080072 | intestinal pseudo-obstruction | MGI:1345138 | Mus musculus (house mouse) | 24064 | Spry2 | author statement supported by traceable reference |
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| DOID:0060041 | autism spectrum disorder | MGI:88276 | Mus musculus (house mouse) | 12387 | Ctnnb1 | author statement supported by traceable reference |
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| DOID:0090014 | severe combined immunodeficiency 104 | MGI:1345961 | Mus musculus (house mouse) | 12721 | Coro1a | author statement supported by traceable reference |
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| DOID:0110858 | polycystic kidney disease 1 | MGI:97603 | Mus musculus (house mouse) | 18763 | Pkd1 | author statement supported by traceable reference |
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| DOID:0050545 | visceral heterotaxy | MGI:2664387 | Mus musculus (house mouse) | 214766 | Mmp21 | author statement supported by traceable reference |
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| DOID:2746 | glycogen storage disease V | MGI:97830 | Mus musculus (house mouse) | 19309 | Pygm | author statement supported by traceable reference |
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| DOID:0050791 | persistent Mullerian duct syndrome | MGI:105062 | Mus musculus (house mouse) | 110542 | Amhr2 | author statement supported by traceable reference |
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| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna | author statement supported by traceable reference |
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| DOID:0060041 | autism spectrum disorder | MGI:97531 | Mus musculus (house mouse) | 18596 | Pdgfrb | author statement supported by traceable reference |
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| DOID:14330 | Parkinson's disease | MGI:94924 | Mus musculus (house mouse) | 13489 | Drd2 | author statement supported by traceable reference |
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| DOID:3312 | bipolar disorder | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 | author statement supported by traceable reference |
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| DOID:0110939 | autosomal recessive osteopetrosis 5 | MGI:2655574 | Mus musculus (house mouse) | 14628 | Ostm1 | author statement supported by traceable reference |
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