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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0060877 | bullous congenital ichthyosiform erythroderma | HGNC:6439 | Homo sapiens (human) | 3849 | KRT2 |
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| DOID:0050883 | infantile cerebellar-retinal degeneration | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0050679 | blue cone monochromacy | HGNC:4206 | Homo sapiens (human) | 2652 | OPN1MW |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0060693 | Brunner Syndrome | HGNC:6833 | Homo sapiens (human) | 4128 | MAOA |
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| DOID:0080245 | Galloway-Mowat syndrome 3 | HGNC:18028 | Homo sapiens (human) | 55644 | OSGEP |
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| DOID:2935 | Chediak-Higashi syndrome | HGNC:1968 | Homo sapiens (human) | 1130 | LYST |
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| DOID:0081423 | familial focal epilepsy with variable foci 3 | HGNC:14124 | Homo sapiens (human) | 8131 | NPRL3 |
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| DOID:0090125 | brain small vessel disease 1 | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0060843 | hereditary neuropathy with liability to pressure palsies | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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| DOID:0110816 | hereditary spastic paraplegia 7 | HGNC:11237 | Homo sapiens (human) | 6687 | SPG7 |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:2030 | anxiety disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:0070005 | Seckel syndrome 9 | HGNC:30764 | Homo sapiens (human) | 10293 | TRAIP |
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| DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0110847 | xeroderma pigmentosum variant type | HGNC:9181 | Homo sapiens (human) | 5429 | POLH |
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| DOID:0060696 | hyperekplexia 1 | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0111742 | cerebellar ataxia type 42 | HGNC:1394 | Homo sapiens (human) | 8913 | CACNA1G |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:0060776 | congenital diarrhea 5 with tufting enteropathy | HGNC:11529 | Homo sapiens (human) | 4072 | EPCAM |
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| DOID:0110151 | Charcot-Marie-Tooth disease type 1C | HGNC:16841 | Homo sapiens (human) | 9516 | LITAF |
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| DOID:0060540 | Hermansky-Pudlak syndrome 2 | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:0112245 | focal segmental glomerulosclerosis 3 | HGNC:14258 | Homo sapiens (human) | 23607 | CD2AP |
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| DOID:0050958 | spinocerebellar ataxia type 7 | HGNC:10560 | Homo sapiens (human) | 6314 | ATXN7 |
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