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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:0110513 | autosomal recessive nonsyndromic deafness 61 | MGI:1933154 | Mus musculus (house mouse) | 80979 | Slc26a5 |
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| DOID:1459 | hypothyroidism | MGI:1933154 | Mus musculus (house mouse) | 80979 | Slc26a5 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:166 | Homo sapiens (human) | 81 | ACTN4 |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:166 | Homo sapiens (human) | 81 | ACTN4 |
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| DOID:162 | cancer | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:11723 | Duchenne muscular dystrophy | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:0110639 | congenital muscular dystrophy due to integrin alpha-7 deficiency | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:0080000 | muscular disease | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:0050700 | cardiomyopathy | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:2349 | arteriosclerosis | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:1826 | epilepsy | RGD:71022 | Rattus norvegicus (Norway rat) | 81008 | Itga7 |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:0060260 | ptosis | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:0090102 | autosomal dominant macrothrombocytopenia TUBB1-related | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:13934 | facial paralysis | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:0112227 | tubulinopathy | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:127 | leiomyoma | HGNC:16265 | Homo sapiens (human) | 81029 | WNT5B |
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| DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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| DOID:0110645 | long QT syndrome 2 | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:2843 | long QT syndrome | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:10273 | heart conduction disease | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:4194 | glucose metabolism disease | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:1826 | epilepsy | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:0050793 | short QT syndrome | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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