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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB ▼ | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:13603 | obstructive jaundice | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:13544 | low tension glaucoma | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | Xenbase:XB-GENE-1006906 | Xenopus tropicalis (tropical clawed frog) | 100490100 | pomt2 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | Xenbase:XB-GENE-494529 | Xenopus tropicalis (tropical clawed frog) | 595052 | alg2 |
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| DOID:90 | degenerative disc disease | MGI:1861437 | Mus musculus (house mouse) | 56637 | Gsk3b |
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| DOID:3393 | coronary artery disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:9351 | diabetes mellitus | Xenbase:XB-GENE-6252363 | Xenopus laevis (African clawed frog) | 378696 | ins.S |
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| DOID:1407 | anterior uveitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:299 | adenocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1793 | pancreatic cancer | Xenbase:XB-GENE-5796042 | Xenopus laevis (African clawed frog) | 734685 | a4gnt.L |
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| DOID:0060589 | Yunis-Varon syndrome | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:1485 | cystic fibrosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:13544 | low tension glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:14067 | Plasmodium falciparum malaria | RGD:2307241 | Rattus norvegicus (Norway rat) | 100301568 | Abo |
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| DOID:1380 | endometrial cancer | FB:FBgn0036842 | Drosophila melanogaster (fruit fly) | 40079 | Ugt316A1 |
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| DOID:8725 | vascular dementia | FB:FBgn0003371 | Drosophila melanogaster (fruit fly) | 31248 | sgg |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | RGD:1310810 | Rattus norvegicus (Norway rat) | 306549 | Pomk |
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| DOID:4947 | cholangiocarcinoma | FB:FBgn0040250 | Drosophila melanogaster (fruit fly) | 53501 | Ugt304A1 |
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| DOID:8466 | retinal degeneration | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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