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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
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:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | FB:FBgn0001991 | Drosophila melanogaster (fruit fly) | 34950 | Ca-alpha1D |
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| DOID:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | MGI:103013 | Mus musculus (house mouse) | 12288 | Cacna1c |
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| DOID:0070529 | Sifrim-Hitz-Weiss syndrome | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:0070529 | Sifrim-Hitz-Weiss syndrome | MGI:1344380 | Mus musculus (house mouse) | 107932 | Chd4 |
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| DOID:0070526 | PLACK syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:0070526 | PLACK syndrome | MGI:1098236 | Mus musculus (house mouse) | 12380 | Cast |
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| DOID:0070525 | peeling skin syndrome 6 | HGNC:33276 | Homo sapiens (human) | 388698 | FLG2 |
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| DOID:0070525 | peeling skin syndrome 6 | MGI:3645678 | Mus musculus (house mouse) | 229574 | Flg2 |
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| DOID:0070524 | peeling skin syndrome 5 | WB:WBGene00005642 | Caenorhabditis elegans | 178585 | srp-1 |
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| DOID:0070524 | peeling skin syndrome 5 | WB:WBGene00005647 | Caenorhabditis elegans | 179125 | srp-6 |
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| DOID:0070524 | peeling skin syndrome 5 | WB:WBGene00005648 | Caenorhabditis elegans | 179195 | srp-7 |
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| DOID:0070521 | peeling skin syndrome 2 | HGNC:11781 | Homo sapiens (human) | 9333 | TGM5 |
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| DOID:0070520 | peeling skin syndrome 1 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | MGI:108186 | Mus musculus (house mouse) | 110695 | Aldh7a1 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0070517 | retinal macular dystrophy 2 | ZFIN:ZDB-GENE-030131-1577 | Danio rerio (zebrafish) | 322857 | prom1a |
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| DOID:0070517 | retinal macular dystrophy 2 | WB:WBGene00008571 | Caenorhabditis elegans | 181330 | prmn-1 |
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| DOID:0070517 | retinal macular dystrophy 2 | MGI:1100886 | Mus musculus (house mouse) | 19126 | Prom1 |
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| DOID:0070517 | retinal macular dystrophy 2 | FB:FBgn0026189 | Drosophila melanogaster (fruit fly) | 38372 | promL |
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| DOID:0070517 | retinal macular dystrophy 2 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | Acox1 |
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| DOID:0070516 | Mitchell syndrome | MGI:1934852 | Mus musculus (house mouse) | 93732 | Acox2 |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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| DOID:0070516 | Mitchell syndrome | SGD:S000003173 | Saccharomyces cerevisiae S288C | 852667 | POX1 |
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