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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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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:0111448 | progressive myoclonus epilepsy 1B | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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| DOID:2752 | glycogen storage disease II | HGNC:4065 | Homo sapiens (human) | 2548 | GAA |
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| DOID:13884 | sick sinus syndrome | HGNC:16882 | Homo sapiens (human) | 10021 | HCN4 |
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| DOID:0050946 | Charlevoix-Saguenay spastic ataxia | HGNC:10519 | Homo sapiens (human) | 26278 | SACS |
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| DOID:0060354 | Stormorken syndrome | HGNC:11386 | Homo sapiens (human) | 6786 | STIM1 |
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| DOID:0110916 | hereditary spherocytosis type 1 | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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| DOID:0110107 | atrial heart septal defect 2 | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:0111015 | Newfoundland cone-rod dystrophy | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:0070443 | neurodevelopmental disorder with cerebellar atrophy and motor dysfunction | HGNC:20043 | Homo sapiens (human) | 25929 | GEMIN5 |
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| DOID:0090115 | spinocerebellar ataxia with axonal neuropathy 1 | HGNC:18884 | Homo sapiens (human) | 55775 | TDP1 |
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| DOID:13628 | favism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0050452 | mevalonic aciduria | HGNC:7530 | Homo sapiens (human) | 4598 | MVK |
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| DOID:0081441 | Nicolaides-Baraitser syndrome | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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| DOID:0050722 | PHGDH deficiency | HGNC:8923 | Homo sapiens (human) | 26227 | PHGDH |
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| DOID:0090114 | Sorsby's fundus dystrophy | HGNC:11822 | Homo sapiens (human) | 7078 | TIMP3 |
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| DOID:0110130 | Bardet-Biedl syndrome 8 | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0111220 | centronuclear myopathy 2 | HGNC:1052 | Homo sapiens (human) | 274 | BIN1 |
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| DOID:0070025 | X-linked dyskeratosis congenita | HGNC:2890 | Homo sapiens (human) | 1736 | DKC1 |
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| DOID:0110365 | retinitis pigmentosa 28 | HGNC:25808 | Homo sapiens (human) | 84140 | FAM161A |
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| DOID:0060796 | hypomyelinating leukodystrophy 12 | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:0112164 | spermatogenic failure 46 | HGNC:2952 | Homo sapiens (human) | 1769 | DNAH8 |
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| DOID:0090017 | epidermolysis bullosa simplex with muscular dystrophy | HGNC:9069 | Homo sapiens (human) | 5339 | PLEC |
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| DOID:0060201 | amyotrophic lateral sclerosis type 10 | HGNC:11571 | Homo sapiens (human) | 23435 | TARDBP |
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| DOID:0050681 | Borjeson-Forssman-Lehmann syndrome | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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