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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:0080052 | acromesomelic dysplasia, Grebe type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080788 | proximal symphalangism 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0050794 | multiple synostoses syndrome | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0081318 | multiple synostoses syndrome 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:14330 | Parkinson's disease | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110977 | brachydactyly type A1C | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0050790 | fibular hypoplasia and complex brachydactyly | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110964 | brachydactyly type A1 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0081317 | multiple synostoses syndrome 1 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110970 | brachydactyly type C | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:10283 | prostate cancer | HGNC:7670 | Homo sapiens (human) | 8202 | NCOA3 |
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| DOID:3459 | breast carcinoma | HGNC:7670 | Homo sapiens (human) | 8202 | NCOA3 |
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| DOID:1612 | breast cancer | HGNC:7670 | Homo sapiens (human) | 8202 | NCOA3 |
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| DOID:9970 | obesity | HGNC:7670 | Homo sapiens (human) | 8202 | NCOA3 |
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| DOID:0080205 | CAKUT | HGNC:8001 | Homo sapiens (human) | 8204 | NRIP1 |
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| DOID:11476 | osteoporosis | HGNC:8001 | Homo sapiens (human) | 8204 | NRIP1 |
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| DOID:10283 | prostate cancer | HGNC:1911 | Homo sapiens (human) | 8208 | CHAF1B |
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| DOID:3070 | high grade glioma | HGNC:1911 | Homo sapiens (human) | 8208 | CHAF1B |
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| DOID:3068 | glioblastoma | HGNC:1911 | Homo sapiens (human) | 8208 | CHAF1B |
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| DOID:8923 | skin melanoma | HGNC:1911 | Homo sapiens (human) | 8208 | CHAF1B |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1911 | Homo sapiens (human) | 8208 | CHAF1B |
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| DOID:9970 | obesity | HGNC:1473 | Homo sapiens (human) | 821 | CANX |
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| DOID:12583 | velocardiofacial syndrome | HGNC:16817 | Homo sapiens (human) | 8220 | ESS2 |
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