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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:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1289 | neurodegenerative disease | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0080695 | Burn-McKeown syndrome | HGNC:30551 | Homo sapiens (human) | 10907 | TXNL4A |
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| DOID:162 | cancer | HGNC:30551 | Homo sapiens (human) | 10907 | TXNL4A |
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| DOID:0110612 | primary ciliary dyskinesia 10 | MGI:1923566 | Mus musculus (house mouse) | 109065 | Dnaaf2 |
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| DOID:399 | tuberculosis | MGI:1923364 | Mus musculus (house mouse) | 109032 | Sp110 |
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| DOID:0112254 | hepatic venoocclusive disease with immunodeficiency | MGI:1923364 | Mus musculus (house mouse) | 109032 | Sp110 |
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| DOID:1289 | neurodegenerative disease | HGNC:24307 | Homo sapiens (human) | 10903 | MTMR11 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:19874 | Homo sapiens (human) | 10902 | BRD8 |
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| DOID:1470 | major depressive disorder | HGNC:234 | Homo sapiens (human) | 109 | ADCY3 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | MGI:1922066 | Mus musculus (house mouse) | 108989 | Tpr |
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| DOID:1324 | lung cancer | MGI:1922066 | Mus musculus (house mouse) | 108989 | Tpr |
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| DOID:0060058 | lymphoma | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:0111988 | immunodeficiency 12 | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9452 | steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9970 | obesity | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:6000 | congestive heart failure | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050855 | renal fibrosis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1909 | melanoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:11446 | sciatic neuropathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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