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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:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:1596 | depressive disorder | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:2841 | asthma | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:557 | kidney disease | HGNC:19069 | Homo sapiens (human) | 57733 | GBA3 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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| DOID:1485 | cystic fibrosis | HGNC:18967 | Homo sapiens (human) | 9695 | EDEM1 |
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| DOID:0050700 | cardiomyopathy | HGNC:18860 | Homo sapiens (human) | 56624 | ASAH2 |
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| DOID:9970 | obesity | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:0050700 | cardiomyopathy | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:1883 | hepatitis C | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:4231 | histiocytoma | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:11168 | anogenital venereal wart | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:399 | tuberculosis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:9970 | obesity | HGNC:18646 | Homo sapiens (human) | 51144 | HSD17B12 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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