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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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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:0070185 | X-linked spermatogenic failure 2 | SGD:S000001335 | Saccharomyces cerevisiae S288C | 854737 | SPO22 |
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| DOID:0050554 | X-linked sideroblastic anemia with ataxia | HGNC:48 | Homo sapiens (human) | 22 | ABCB7 |
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| DOID:0112128 | X-linked severe congenital neutropenia | SGD:S000005707 | Saccharomyces cerevisiae S288C | 854353 | LAS17 |
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| DOID:0060013 | X-linked severe combined immunodeficiency | HGNC:6010 | Homo sapiens (human) | 3561 | IL2RG |
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| DOID:0060013 | X-linked severe combined immunodeficiency | MGI:96551 | Mus musculus (house mouse) | 16186 | Il2rg |
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| DOID:0112124 | X-linked retinitis pigmentosa and sinorespiratory infections | MGI:1344037 | Mus musculus (house mouse) | 19893 | Rpgr |
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| DOID:0111834 | X-linked reticulate pigmentary disorder | HGNC:9173 | Homo sapiens (human) | 5422 | POLA1 |
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| DOID:0111834 | X-linked reticulate pigmentary disorder | SGD:S000005046 | Saccharomyces cerevisiae S288C | 855621 | POL1 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0111768 | X-linked properdin deficiency | MGI:97545 | Mus musculus (house mouse) | 18636 | Cfp |
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| DOID:0111768 | X-linked properdin deficiency | HGNC:8864 | Homo sapiens (human) | 5199 | CFP |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:0111779 | X-linked panhypopituitarism | MGI:98357 | Mus musculus (house mouse) | 20664 | Sox1 |
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| DOID:0050566 | X-linked nonsyndromic deafness | MGI:1915013 | Mus musculus (house mouse) | 67763 | Prpsap1 |
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| DOID:0050566 | X-linked nonsyndromic deafness | HGNC:9466 | Homo sapiens (human) | 5635 | PRPSAP1 |
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| DOID:0111798 | X-linked nephrolithiasis type I | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0111798 | X-linked nephrolithiasis type I | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | WB:WBGene00011582 | Caenorhabditis elegans | 188227 | ntr-1 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | RGD:2186 | Rattus norvegicus (Norway rat) | 25108 | Avpr2 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | MGI:88123 | Mus musculus (house mouse) | 12000 | Avpr2 |
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| DOID:0112012 | X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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