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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:8893 | psoriasis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:10652 | Alzheimer's disease | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0060295 | complement component 2 deficiency | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:1407 | anterior uveitis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0110521 | autosomal recessive nonsyndromic deafness 70 | MGI:1918951 | Mus musculus (house mouse) | 71701 | Pnpt1 |
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| DOID:0111467 | combined oxidative phosphorylation deficiency 13 | MGI:1918951 | Mus musculus (house mouse) | 71701 | Pnpt1 |
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| DOID:0050974 | spinocerebellar ataxia type 25 | MGI:1918951 | Mus musculus (house mouse) | 71701 | Pnpt1 |
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| DOID:3347 | osteosarcoma | MGI:1918952 | Mus musculus (house mouse) | 71702 | Cdc5l |
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| DOID:1574 | alcohol use disorder | MGI:1918952 | Mus musculus (house mouse) | 71702 | Cdc5l |
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| DOID:4914 | esophagus adenocarcinoma | MGI:1918952 | Mus musculus (house mouse) | 71702 | Cdc5l |
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| DOID:2218 | blood platelet disease | HGNC:12013 | Homo sapiens (human) | 7171 | TPM4 |
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| DOID:0080236 | autosomal dominant intellectual developmental disorder 45 | MGI:1918972 | Mus musculus (house mouse) | 71722 | Cic |
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| DOID:150 | disease of mental health | MGI:1918972 | Mus musculus (house mouse) | 71722 | Cic |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:0112186 | thyroid dyshormonogenesis 2A | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:2921 | glomerulonephritis | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:612 | primary immunodeficiency disease | HGNC:12016 | Homo sapiens (human) | 7174 | TPP2 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:12017 | Homo sapiens (human) | 7175 | TPR |
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| DOID:1324 | lung cancer | HGNC:12017 | Homo sapiens (human) | 7175 | TPR |
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| DOID:11252 | microcytic anemia | MGI:1919003 | Mus musculus (house mouse) | 71753 | Tmprss6 |
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| DOID:3525 | middle cerebral artery infarction | MGI:1919020 | Mus musculus (house mouse) | 71770 | Ap2b1 |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | MGI:1919025 | Mus musculus (house mouse) | 71775 | Inhca |
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| DOID:5844 | myocardial infarction | MGI:1919035 | Mus musculus (house mouse) | 71785 | Pdgfd |
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