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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:11984 | hypertrophic cardiomyopathy | HGNC:1402 | Homo sapiens (human) | 783 | CACNB2 |
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| DOID:2316 | brain ischemia | HGNC:1131 | Homo sapiens (human) | 7832 | BTG2 |
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| DOID:1612 | breast cancer | HGNC:1131 | Homo sapiens (human) | 7832 | BTG2 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:1131 | Homo sapiens (human) | 7832 | BTG2 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:1131 | Homo sapiens (human) | 7832 | BTG2 |
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| DOID:4450 | renal cell carcinoma | HGNC:1131 | Homo sapiens (human) | 7832 | BTG2 |
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| DOID:0080612 | anterior segment dysgenesis 7 | HGNC:14966 | Homo sapiens (human) | 7837 | PXDN |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:428 | Homo sapiens (human) | 7840 | ALMS1 |
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| DOID:0050473 | Alstrom syndrome | HGNC:428 | Homo sapiens (human) | 7840 | ALMS1 |
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| DOID:9970 | obesity | HGNC:428 | Homo sapiens (human) | 7840 | ALMS1 |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:2490 | congenital nervous system abnormality | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0112234 | microlissencephaly | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0080918 | polymicrogyria | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:10907 | microcephaly | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0112232 | lissencephaly 3 | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:14250 | Down syndrome | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0050453 | lissencephaly | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:11832 | visual epilepsy | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0050328 | congenital hypothyroidism | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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| DOID:0070124 | congenital nongoitrous hypothyroidism 2 | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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| DOID:3910 | lung adenocarcinoma | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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| DOID:1324 | lung cancer | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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| DOID:0050686 | organ system cancer | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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| DOID:4947 | cholangiocarcinoma | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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