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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:10595 | Charcot-Marie-Tooth disease | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:8778 | Crohn's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110704 | hypotrichosis 7 | HGNC:18483 | Homo sapiens (human) | 200879 | LIPH |
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| DOID:3829 | pituitary adenoma | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:0110077 | arrhythmogenic right ventricular dysplasia 9 | HGNC:9024 | Homo sapiens (human) | 5318 | PKP2 |
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| DOID:9256 | colorectal cancer | HGNC:1149 | Homo sapiens (human) | 701 | BUB1B |
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| DOID:7148 | rheumatoid arthritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6005 | Homo sapiens (human) | 59067 | IL21 |
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| DOID:3307 | teratoma | HGNC:7849 | Homo sapiens (human) | 4830 | NME1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:13746 | Homo sapiens (human) | 57795 | BRINP2 |
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| DOID:9286 | priapism | HGNC:3531 | Homo sapiens (human) | 2162 | F13A1 |
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| DOID:0111158 | SADDAN | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | HGNC:4573 | Homo sapiens (human) | 2892 | GRIA3 |
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| DOID:1588 | thrombocytopenia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:5614 | eye disease | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0081354 | congenital myopathy 22A | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:552 | pneumonia | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0080299 | partial lipodystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:13550 | angle-closure glaucoma | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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