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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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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 | July 29, 2024 |
| Disease ID ▲ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | MGI:2442480 | Mus musculus (house mouse) | 230801 | Pigv |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | FB:FBgn0265174 | Drosophila melanogaster (fruit fly) | 19835383 | PIG-V |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | ZFIN:ZDB-GENE-121116-1 | Danio rerio (zebrafish) | 100148642 | pigv |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | RGD:1309526 | Rattus norvegicus (Norway rat) | 366478 | Pigv |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | FB:FBgn0031284 | Drosophila melanogaster (fruit fly) | 33258 | PGAP2 |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | FB:FBgn0033088 | Drosophila melanogaster (fruit fly) | 35570 | PGAP3 |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0070467 | carpal tunnel syndrome 2 | FB:FBgn0031850 | Drosophila melanogaster (fruit fly) | 33941 | Tsp | CG11326 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | Xenbase:XB-GENE-984155 | Xenopus laevis (African clawed frog) | 447370 | ogdhl.L |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | MGI:1098267 | Mus musculus (house mouse) | 18293 | Ogdh |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | RGD:1561359 | Rattus norvegicus (Norway rat) | 360975 | Ogdh |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | 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 | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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