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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:9538 | multiple myeloma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:0050746 | mantle cell lymphoma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:905 | Zellweger syndrome | HGNC:8853 | Homo sapiens (human) | 8799 | PEX11B |
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| DOID:0081274 | peroxisome biogenesis disorder 14B | HGNC:8853 | Homo sapiens (human) | 8799 | PEX11B |
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| DOID:0110428 | dilated cardiomyopathy 1AA | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:0081342 | congenital myopathy 8 | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | HGNC:11448 | Homo sapiens (human) | 8803 | SUCLA2 |
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| DOID:2841 | asthma | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:850 | lung disease | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | HGNC:3006 | Homo sapiens (human) | 8818 | DPM2 |
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| DOID:0090082 | hypogonadotropic hypogonadism 20 with or without anosmia | HGNC:3673 | Homo sapiens (human) | 8822 | FGF17 |
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| DOID:0080425 | developmental and epileptic encephalopathy 47 | HGNC:3672 | Homo sapiens (human) | 8823 | FGF16 |
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| DOID:0111813 | syndactyly type 8 | HGNC:3672 | Homo sapiens (human) | 8823 | FGF16 |
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| DOID:0060041 | autism spectrum disorder | HGNC:8005 | Homo sapiens (human) | 8828 | NRP2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8004 | Homo sapiens (human) | 8829 | NRP1 |
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| DOID:6419 | tetralogy of Fallot | HGNC:8004 | Homo sapiens (human) | 8829 | NRP1 |
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