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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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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:0060825 | Christianson syndrome | SGD:S000002864 | Saccharomyces cerevisiae S288C | 852066 | NHX1 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | RGD:70958 | Rattus norvegicus (Norway rat) | 29628 | Gria3 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | WB:WBGene00001613 | Caenorhabditis elegans | 175999 | glr-2 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | WB:WBGene00001612 | Caenorhabditis elegans | 176204 | glr-1 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | HGNC:4573 | Homo sapiens (human) | 2892 | GRIA3 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | MGI:95810 | Mus musculus (house mouse) | 53623 | Gria3 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | FB:FBgn0004619 | Drosophila melanogaster (fruit fly) | 38742 | GluRIA |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | HGNC:2555 | Homo sapiens (human) | 8450 | CUL4B |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | MGI:1919834 | Mus musculus (house mouse) | 72584 | Cul4b |
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| DOID:0060821 | syndromic X-linked intellectual disability 14 | HGNC:20439 | Homo sapiens (human) | 65109 | UPF3B |
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| DOID:0060817 | syndromic X-linked intellectual disability 34 | MGI:1855692 | Mus musculus (house mouse) | 53610 | Nono |
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| DOID:0060817 | syndromic X-linked intellectual disability 34 | HGNC:7871 | Homo sapiens (human) | 4841 | NONO |
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| DOID:0060814 | Wilson-Turner syndrome | HGNC:25726 | Homo sapiens (human) | 81887 | LAS1L |
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| DOID:0060814 | Wilson-Turner syndrome | MGI:1923380 | Mus musculus (house mouse) | 76130 | Las1l |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | HGNC:20672 | Homo sapiens (human) | 23133 | PHF8 |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | MGI:2444341 | Mus musculus (house mouse) | 320595 | Phf8 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | MGI:1926884 | Mus musculus (house mouse) | 59026 | Huwe1 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | RGD:69231 | Rattus norvegicus (Norway rat) | 63864 | Hsd17b10 |
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| DOID:0060809 | syndromic X-linked intellectual disability Claes-Jensen type | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0060807 | syndromic X-linked intellectual disability Najm type | SGD:S000006125 | Saccharomyces cerevisiae S288C | 855897 | HRR25 |
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| DOID:0060807 | syndromic X-linked intellectual disability Najm type | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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| DOID:0060807 | syndromic X-linked intellectual disability Najm type | MGI:1355272 | Mus musculus (house mouse) | 104318 | Csnk1d |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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