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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:7998 | hyperthyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:5212 | congenital disorder of glycosylation | ZFIN:ZDB-GENE-050417-236 | Danio rerio (zebrafish) | 550425 | b4galt1 |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-041124-3 | Danio rerio (zebrafish) | 493780 | ext2 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:104872 | Mus musculus (house mouse) | 19047 | Ppp1cc |
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| DOID:0080552 | congenital disorder of glycosylation Ia | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:9408 | acute myocardial infarction | MGI:1861437 | Mus musculus (house mouse) | 56637 | Gsk3b |
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| DOID:2018 | hyperinsulinism | RGD:2916 | Rattus norvegicus (Norway rat) | 24506 | Ins2 |
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| DOID:0080199 | colorectal carcinoma | SGD:S000002779 | Saccharomyces cerevisiae S288C | 851977 | CTS2 |
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| DOID:1459 | hypothyroidism | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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| DOID:13580 | cholestasis | FB:FBgn0004507 | Drosophila melanogaster (fruit fly) | 33386 | Glyp |
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| DOID:1793 | pancreatic cancer | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:14250 | Down syndrome | MGI:1916863 | Mus musculus (house mouse) | 80294 | Pofut2 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:2841 | asthma | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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| DOID:8398 | osteoarthritis | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:10140 | dry eye syndrome | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:9452 | steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0111043 | glycogen storage disease IXc | RGD:620024 | Rattus norvegicus (Norway rat) | 140671 | Phkg2 |
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| DOID:0014667 | disease of metabolism | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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