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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:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | Xenbase:XB-GENE-17340884 | Xenopus laevis (African clawed frog) | 108712551 | large1.S |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | Xenbase:XB-GENE-6250446 | Xenopus tropicalis (tropical clawed frog) | 100498555 | large1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | RGD:1308895 | Rattus norvegicus (Norway rat) | 361368 | Large1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | ZFIN:ZDB-GENE-061204-1 | Danio rerio (zebrafish) | 446213 | large1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0111254 | glutaric acidemia I | HGNC:4189 | Homo sapiens (human) | 2639 | GCDH |
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| DOID:0111257 | gamma-glutamyl transpeptidase deficiency | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:0111258 | pentosuria | MGI:1915130 | Mus musculus (house mouse) | 67880 | Dcxr |
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| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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| DOID:0111258 | pentosuria | WB:WBGene00000984 | Caenorhabditis elegans | 179741 | dhs-21 |
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| DOID:0111258 | pentosuria | RGD:620031 | Rattus norvegicus (Norway rat) | 171408 | Dcxr |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0111334 | congenital leptin deficiency | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0111334 | congenital leptin deficiency | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:0111334 | congenital leptin deficiency | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:0111343 | lateral meningocele syndrome | FB:FBgn0004647 | Drosophila melanogaster (fruit fly) | 31293 | N | CG3936 |
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| DOID:0111352 | D-2-hydroxyglutaric aciduria 2 | SGD:S000004954 | Saccharomyces cerevisiae S288C | 855723 | IDP3 |
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