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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:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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| DOID:0111626 | D-glyceric aciduria | RGD:1591498 | Rattus norvegicus (Norway rat) | 684314 | Glyctk |
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| DOID:0111626 | D-glyceric aciduria | MGI:2444085 | Mus musculus (house mouse) | 235582 | Glyctk |
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| DOID:0111630 | familial erythrocytosis 8 | SGD:S000001635 | Saccharomyces cerevisiae S288C | 853705 | GPM1 |
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| DOID:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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| DOID:0111630 | familial erythrocytosis 8 | MGI:1098242 | Mus musculus (house mouse) | 12183 | Bpgm |
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| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:0111646 | congenital lactase deficiency | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0111673 | Saul-Wilson syndrome | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:0111680 | essential fructosuria | MGI:1096353 | Mus musculus (house mouse) | 16548 | Khk |
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| DOID:0111680 | essential fructosuria | HGNC:6315 | Homo sapiens (human) | 3795 | KHK |
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| DOID:0111680 | essential fructosuria | RGD:2966 | Rattus norvegicus (Norway rat) | 25659 | Khk |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | RGD:619868 | Rattus norvegicus (Norway rat) | 25283 | Gclc |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0111739 | X-linked deafness 1 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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