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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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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 | July 29, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0112315 | brain small vessel disease 3 | WB:WBGene00008426 | Caenorhabditis elegans | 3565069 | D2045.9 |
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| DOID:0112315 | brain small vessel disease 3 | Xenbase:XB-GENE-952958 | Xenopus laevis (African clawed frog) | 100125229 | colgalt1.L |
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| DOID:0112315 | brain small vessel disease 3 | MGI:1924348 | Mus musculus (house mouse) | 234407 | Colgalt1 |
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| DOID:0112315 | brain small vessel disease 3 | ZFIN:ZDB-GENE-070424-114 | Danio rerio (zebrafish) | 567859 | colgalt1b |
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| DOID:0112313 | brain small vessel disease | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:0112313 | brain small vessel disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0112313 | brain small vessel disease | RGD:628827 | Rattus norvegicus (Norway rat) | 252917 | Nr1d1 |
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| DOID:0112313 | brain small vessel disease | MGI:2444210 | Mus musculus (house mouse) | 217166 | Nr1d1 |
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| DOID:0112303 | spondylometaphyseal dysplasia with corneal dystrophy | HGNC:9056 | Homo sapiens (human) | 5331 | PLCB3 |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0112298 | spondylometaphyseal dysplasia Sedaghatian type | SGD:S000000448 | Saccharomyces cerevisiae S288C | 852546 | GPX2 |
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| DOID:0112298 | spondylometaphyseal dysplasia Sedaghatian type | SGD:S000001509 | Saccharomyces cerevisiae S288C | 853842 | GPX1 |
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| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | Xenbase:XB-GENE-990439 | Xenopus tropicalis (tropical clawed frog) | 407846 | st6gal2 |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | RGD:2082 | Rattus norvegicus (Norway rat) | 25233 | Akt2 |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | MGI:104874 | Mus musculus (house mouse) | 11652 | Akt2 |
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| DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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| DOID:0112250 | Gaucher's disease type IIIC | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:0112248 | 17-beta hydroxysteroid dehydrogenase 3 deficiency | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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