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GlyTouCan
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
LM-GlycoRepo
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:0080264 | exudative vitreoretinopathy 7 | RGD:70487 | Rattus norvegicus (Norway rat) | 84353 | Ctnnb1 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | MGI:1347520 | Mus musculus (house mouse) | 26563 | Ror1 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | HGNC:10256 | Homo sapiens (human) | 4919 | ROR1 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | FB:FBgn0010407 | Drosophila melanogaster (fruit fly) | 34367 | Ror |
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| DOID:0080262 | autosomal recessive nonsyndromic deafness 107 | MGI:104709 | Mus musculus (house mouse) | 22378 | Wbp2 |
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| DOID:0080261 | autosomal recessive nonsyndromic deafness 106 | HGNC:21296 | Homo sapiens (human) | 64787 | EPS8L2 |
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| DOID:0080260 | autosomal recessive spinocerebellar ataxia 26 | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0080259 | autosomal recessive spinocerebellar ataxia 25 | FB:FBgn0029943 | Drosophila melanogaster (fruit fly) | 31666 | Atg5 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0080257 | autosomal recessive congenital ichthyosis 13 | HGNC:29958 | Homo sapiens (human) | 121214 | SDR9C7 |
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| DOID:0080254 | orofaciodigital syndrome XVI | MGI:1914160 | Mus musculus (house mouse) | 66910 | Tmem107 |
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| DOID:0080254 | orofaciodigital syndrome XVI | RGD:1595972 | Rattus norvegicus (Norway rat) | 691750 | Tmem107 |
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| DOID:0080254 | orofaciodigital syndrome XVI | HGNC:28128 | Homo sapiens (human) | 84314 | TMEM107 |
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| DOID:0080254 | orofaciodigital syndrome XVI | Xenbase:XB-GENE-6254265 | Xenopus laevis (African clawed frog) | 735183 | tmem107.L |
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| DOID:0080253 | Meckel syndrome 13 | Xenbase:XB-GENE-6254265 | Xenopus laevis (African clawed frog) | 735183 | tmem107.L |
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| DOID:0080253 | Meckel syndrome 13 | MGI:1914160 | Mus musculus (house mouse) | 66910 | Tmem107 |
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| DOID:0080253 | Meckel syndrome 13 | HGNC:28128 | Homo sapiens (human) | 84314 | TMEM107 |
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| DOID:0080253 | Meckel syndrome 13 | RGD:1595972 | Rattus norvegicus (Norway rat) | 691750 | Tmem107 |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0080249 | erythrokeratodermia variabilis et progressiva 3 | MGI:95713 | Mus musculus (house mouse) | 14609 | Gja1 |
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| DOID:0080245 | Galloway-Mowat syndrome 3 | HGNC:18028 | Homo sapiens (human) | 55644 | OSGEP |
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| DOID:0080244 | Galloway-Mowat syndrome 2 | HGNC:26058 | Homo sapiens (human) | 8270 | LAGE3 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | MGI:2661175 | Mus musculus (house mouse) | 245684 | Cnksr2 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | HGNC:19701 | Homo sapiens (human) | 22866 | CNKSR2 |
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