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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:0070070 | autosomal dominant intellectual developmental disorder 40 | MGI:1196398 | Mus musculus (house mouse) | 101994 | Champ1 |
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| DOID:2377 | multiple sclerosis | HGNC:7215 | Homo sapiens (human) | 10198 | MPHOSPH9 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:1574 | alcohol use disorder | HGNC:19071 | Homo sapiens (human) | 10189 | ALYREF |
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| DOID:13099 | Moyamoya disease | MGI:2142149 | Mus musculus (house mouse) | 101772 | Ano1 |
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| DOID:0110567 | autosomal dominant nonsyndromic deafness 41 | Xenbase:XB-GENE-6043718 | Xenopus tropicalis (tropical clawed frog) | 101730278 | p2rx2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:9273 | citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0070342 | adult-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:4137 | common bile duct disease | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0110705 | hypotrichosis 8 | HGNC:15520 | Homo sapiens (human) | 10161 | LPAR6 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:10763 | hypertension | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:16746 | Homo sapiens (human) | 10150 | MBNL2 |
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| DOID:0050759 | myotonic dystrophy type 2 | HGNC:16746 | Homo sapiens (human) | 10150 | MBNL2 |
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| DOID:450 | myotonic disease | HGNC:16746 | Homo sapiens (human) | 10150 | MBNL2 |
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