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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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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:0110263 | cataract 19 multiple types | MGI:104698 | Mus musculus (house mouse) | 233187 | Lim2 |
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| DOID:9970 | obesity | HGNC:7958 | Homo sapiens (human) | 4889 | NPY5R |
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| DOID:576 | proteinuria | RGD:2493 | Rattus norvegicus (Norway rat) | 24310 | Ace |
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| DOID:0110703 | hypotrichosis 6 | MGI:2661061 | Mus musculus (house mouse) | 16769 | Dsg4 |
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| DOID:2752 | glycogen storage disease II | MGI:95609 | Mus musculus (house mouse) | 14387 | Gaa |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:57 | Homo sapiens (human) | 368 | ABCC6 |
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| DOID:4621 | holoprosencephaly | HGNC:11776 | Homo sapiens (human) | 7050 | TGIF1 |
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| DOID:4947 | cholangiocarcinoma | RGD:2794 | Rattus norvegicus (Norway rat) | 24446 | Hgf |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:14504 | Niemann-Pick disease | WB:WBGene00003561 | Caenorhabditis elegans | 180719 | ncr-1 |
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| DOID:14504 | Niemann-Pick disease | WB:WBGene00003562 | Caenorhabditis elegans | 176165 | ncr-2 |
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| DOID:9870 | galactosemia | SGD:S000000222 | Saccharomyces cerevisiae S288C | 852306 | GAL7 |
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| DOID:12894 | Sjogren's syndrome | MGI:2676278 | Mus musculus (house mouse) | 239611 | Muc19 |
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| DOID:2717 | Bloom syndrome | HGNC:1058 | Homo sapiens (human) | 641 | BLM |
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| DOID:0110142 | Bartter disease type 1 | MGI:103150 | Mus musculus (house mouse) | 20495 | Slc12a1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:11476 | osteoporosis | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:6000 | congestive heart failure | RGD:621316 | Rattus norvegicus (Norway rat) | 81686 | Mmp2 |
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| DOID:1388 | Tangier disease | MGI:99607 | Mus musculus (house mouse) | 11303 | Abca1 |
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| DOID:10763 | hypertension | RGD:67383 | Rattus norvegicus (Norway rat) | 170538 | Prkcd |
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| DOID:0090031 | D-bifunctional protein deficiency | MGI:105089 | Mus musculus (house mouse) | 15488 | Hsd17b4 |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:1838 | Menkes disease | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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