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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:2739 | Gilbert syndrome | Xenbase:XB-GENE-5793241 | Xenopus tropicalis (tropical clawed frog) | 100135191 | ugt1a6 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:10591 | pre-eclampsia | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:2272 | vulvovaginal candidiasis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0050571 | congenital disorder of glycosylation type II | Xenbase:XB-GENE-6486521 | Xenopus laevis (African clawed frog) | 101027298 | galnt2.S |
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| DOID:583 | hemolytic anemia | Xenbase:XB-GENE-5962623 | Xenopus laevis (African clawed frog) | 495825 | abo.3.L |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:4989 | pancreatitis | MGI:109521 | Mus musculus (house mouse) | 15558 | Htr2a |
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| DOID:9744 | type 1 diabetes mellitus | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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| DOID:0090056 | dystonia 12 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:9744 | type 1 diabetes mellitus | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:162 | cancer | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:9008 | psoriatic arthritis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:7147 | ankylosing spondylitis | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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| DOID:1380 | endometrial cancer | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:3021 | acute kidney failure | SGD:S000001509 | Saccharomyces cerevisiae S288C | 853842 | GPX1 |
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| DOID:9409 | diabetes insipidus | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| DOID:0110389 | retinitis pigmentosa 73 | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:162 | cancer | SGD:S000001085 | Saccharomyces cerevisiae S288C | 856439 | DOG2 |
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| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:9884 | muscular dystrophy | RGD:1310087 | Rattus norvegicus (Norway rat) | 362520 | Fktn |
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