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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
LM-GlycoRepo
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:0060340 | ciliopathy | HGNC:26252 | Homo sapiens (human) | 79819 | DNAI4 |
|
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| DOID:0060041 | autism spectrum disorder | ZFIN:ZDB-GENE-100430-2 | Danio rerio (zebrafish) | 798226 | ndst2b |
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| DOID:1059 | intellectual disability | ZFIN:ZDB-GENE-100430-2 | Danio rerio (zebrafish) | 798226 | ndst2b |
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| DOID:14227 | azoospermia | ZFIN:ZDB-GENE-100430-2 | Danio rerio (zebrafish) | 798226 | ndst2b |
|
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| DOID:0060858 | hypotonia-cystinuria syndrome | HGNC:26276 | Homo sapiens (human) | 79823 | CAMKMT |
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| DOID:10605 | short bowel syndrome | HGNC:24039 | Homo sapiens (human) | 79827 | CLMP |
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| DOID:0110726 | neuronal ceroid lipofuscinosis 2 | ZFIN:ZDB-GENE-030131-6654 | Danio rerio (zebrafish) | 798347 | tpp1 |
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| DOID:0080059 | autosomal recessive spinocerebellar ataxia 7 | ZFIN:ZDB-GENE-030131-6654 | Danio rerio (zebrafish) | 798347 | tpp1 |
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| DOID:1793 | pancreatic cancer | ZFIN:ZDB-GENE-080722-3 | Danio rerio (zebrafish) | 798349 | b3galt10.1 |
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| DOID:162 | cancer | HGNC:23786 | Homo sapiens (human) | 79837 | PIP4K2C |
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| DOID:341 | peripheral vascular disease | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:0111072 | myostatin-related muscle hypertrophy | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:332 | amyotrophic lateral sclerosis | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:4676 | uremia | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:1459 | hypothyroidism | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:767 | muscular atrophy | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:6000 | congestive heart failure | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:0070122 | Meckel syndrome 8 | HGNC:25774 | Homo sapiens (human) | 79867 | TCTN2 |
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| DOID:0110993 | Joubert syndrome 24 | HGNC:25774 | Homo sapiens (human) | 79867 | TCTN2 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:25835 | Homo sapiens (human) | 79875 | THSD4 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:26185 | Homo sapiens (human) | 79879 | CCDC134 |
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| DOID:1059 | intellectual disability | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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