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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:0060556 | Kufor-Rakeb syndrome | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:0112348 | hereditary spastic paraplegia 78 | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:0060893 | juvenile-onset Parkinson's disease | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:14503 | neuronal ceroid lipofuscinosis | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:2476 | hereditary spastic paraplegia | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:14330 | Parkinson's disease | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:820 | myocarditis | MGI:1922026 | Mus musculus (house mouse) | 74776 | Ppa2 |
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| DOID:0110633 | rigid spine muscular dystrophy 1 | MGI:2151208 | Mus musculus (house mouse) | 74777 | Selenon |
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| DOID:12858 | Huntington's disease | MGI:1923831 | Mus musculus (house mouse) | 74781 | Wipi2 |
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| DOID:10487 | Hirschsprung's disease | HGNC:12789 | Homo sapiens (human) | 7479 | WNT8B |
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| DOID:0090026 | split hand-foot malformation 6 | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:0050591 | tooth agenesis | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:9970 | obesity | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:4450 | renal cell carcinoma | HGNC:12776 | Homo sapiens (human) | 7481 | WNT11 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:12776 | Homo sapiens (human) | 7481 | WNT11 |
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| DOID:1911 | endodermal sinus tumor | HGNC:12781 | Homo sapiens (human) | 7482 | WNT2B |
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| DOID:3307 | teratoma | HGNC:12781 | Homo sapiens (human) | 7482 | WNT2B |
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| DOID:0060774 | congenital diarrhea | HGNC:12781 | Homo sapiens (human) | 7482 | WNT2B |
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| DOID:4947 | cholangiocarcinoma | HGNC:12778 | Homo sapiens (human) | 7483 | WNT9A |
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| DOID:1793 | pancreatic cancer | HGNC:12778 | Homo sapiens (human) | 7483 | WNT9A |
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| DOID:1612 | breast cancer | HGNC:12778 | Homo sapiens (human) | 7483 | WNT9A |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:3114 | serous cystadenocarcinoma | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:1324 | lung cancer | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:1793 | pancreatic cancer | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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