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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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MIRAGE
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:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:14500 | fucosidosis | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9351 | diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:8947 | diabetic retinopathy | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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| DOID:0081126 | DeSanto-Shinawi syndrome | HGNC:17327 | Homo sapiens (human) | 51322 | WAC |
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| DOID:0111212 | autosomal dominant distal hereditary motor neuronopathy 9 | HGNC:12729 | Homo sapiens (human) | 7453 | WARS1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:12730 | Homo sapiens (human) | 10352 | WARS2 |
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| DOID:0060571 | Ritscher-Schinzel syndrome 1 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:0110823 | hereditary spastic paraplegia 8 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:3310 | atopic dermatitis | HGNC:12735 | Homo sapiens (human) | 8976 | WASL |
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| DOID:9169 | Wiskott-Aldrich syndrome | HGNC:12735 | Homo sapiens (human) | 8976 | WASL |
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| DOID:0080569 | congenital disorder of glycosylation Ir | SGD:S000000728 | Saccharomyces cerevisiae S288C | 856716 | WBP1 |
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| DOID:2935 | Chediak-Higashi syndrome | HGNC:20751 | Homo sapiens (human) | 23001 | WDFY3 |
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| DOID:0070295 | primary autosomal dominant microcephaly 18 | HGNC:20751 | Homo sapiens (human) | 23001 | WDFY3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:20751 | Homo sapiens (human) | 23001 | WDFY3 |
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| DOID:4947 | cholangiocarcinoma | HGNC:23170 | Homo sapiens (human) | 11169 | WDHD1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:12755 | Homo sapiens (human) | 10885 | WDR3 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:25651 | Homo sapiens (human) | 55339 | WDR33 |
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| DOID:0110090 | short-rib thoracic dysplasia 7 with or without polydactyly | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:0080804 | cranioectodermal dysplasia 2 | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:5082 | liver cirrhosis | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:12714 | Ellis-Van Creveld syndrome | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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