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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2841 | asthma | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:12053 | cryptococcosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:0050127 | sinusitis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:10325 | silicosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:1826 | epilepsy | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:224 | transient cerebral ischemia | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:219 | colon cancer | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:10907 | microcephaly | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:0050912 | colon adenoma | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:10907 | microcephaly | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1826 | epilepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:5679 | retinal disease | HGNC:17852 | Homo sapiens (human) | 56994 | CHPT1 |
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| DOID:10763 | hypertension | HGNC:17423 | Homo sapiens (human) | 55501 | CHST12 |
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| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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| DOID:5419 | schizophrenia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:0050852 | limb ischemia | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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