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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
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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:3209 | junctional epidermolysis bullosa | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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| DOID:0110915 | childhood hypophosphatasia | MGI:87983 | Mus musculus (house mouse) | 11647 | Alpl |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:8947 | diabetic retinopathy | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:3770 | pulmonary fibrosis | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:4603 | epidermolytic hyperkeratosis | HGNC:6413 | Homo sapiens (human) | 3858 | KRT10 |
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| DOID:9263 | homocystinuria | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:0110495 | autosomal recessive nonsyndromic deafness 37 | MGI:104785 | Mus musculus (house mouse) | 17920 | Myo6 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8863 | Homo sapiens (human) | 5198 | PFAS |
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| DOID:1407 | anterior uveitis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:9352 | type 2 diabetes mellitus | MGI:87853 | Mus musculus (house mouse) | 50518 | a |
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| DOID:1099 | alpha thalassemia | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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| DOID:13949 | interstitial cystitis | RGD:1598328 | Rattus norvegicus (Norway rat) | 310738 | Ngf |
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| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | FB:FBgn0002921 | Drosophila melanogaster (fruit fly) | 48971 | AtpĪ± |
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| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | FB:FBgn0002921 | Drosophila melanogaster (fruit fly) | 48971 | Atpalpha |
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| DOID:0080570 | congenital disorder of glycosylation It | SGD:S000001610 | Saccharomyces cerevisiae S288C | 853732 | PGM1 |
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| DOID:0080570 | congenital disorder of glycosylation It | SGD:S000004711 | Saccharomyces cerevisiae S288C | 855131 | PGM2 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | FB:FBgn0039827 | Drosophila melanogaster (fruit fly) | 43689 | CG1544 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | FB:FBgn0039827 | Drosophila melanogaster (fruit fly) | 43689 | Oadh |
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| DOID:0070341 | neonatal-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | Aralar |
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| DOID:0070048 | GAND syndrome | MGI:2443225 | Mus musculus (house mouse) | 229542 | Gatad2b |
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