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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:0060571 | Ritscher-Schinzel syndrome 1 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:0110823 | hereditary spastic paraplegia 8 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:1826 | epilepsy | HGNC:20566 | Homo sapiens (human) | 9900 | SV2A |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:20566 | Homo sapiens (human) | 9900 | SV2A |
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| DOID:5419 | schizophrenia | HGNC:19744 | Homo sapiens (human) | 9901 | SRGAP3 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:9884 | muscular dystrophy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:9296 | cleft lip | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050700 | cardiomyopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050453 | lissencephaly | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:22197 | Homo sapiens (human) | 9907 | AP5Z1 |
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| DOID:0110800 | hereditary spastic paraplegia 48 | HGNC:22197 | Homo sapiens (human) | 9907 | AP5Z1 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:24305 | Homo sapiens (human) | 9918 | NCAPD2 |
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| DOID:9970 | obesity | HGNC:29006 | Homo sapiens (human) | 9919 | SEC16A |
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| DOID:0050778 | Meckel syndrome | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
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| DOID:4195 | hyperglycemia | MGI:2139279 | Mus musculus (house mouse) | 99296 | Hrh3 |
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| DOID:1824 | status epilepticus | MGI:2139279 | Mus musculus (house mouse) | 99296 | Hrh3 |
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| DOID:11446 | sciatic neuropathy | MGI:2139279 | Mus musculus (house mouse) | 99296 | Hrh3 |
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| DOID:9970 | obesity | MGI:2139279 | Mus musculus (house mouse) | 99296 | Hrh3 |
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| DOID:10914 | amnestic disorder | MGI:2139279 | Mus musculus (house mouse) | 99296 | Hrh3 |
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