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GlyTouCan
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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:13054 | Homo sapiens (human) | 9203 | ZMYM3 |
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| DOID:0050888 | syndromic intellectual disability | HGNC:9397 | Homo sapiens (human) | 23613 | ZMYND8 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:12886 | Homo sapiens (human) | 64397 | ZNF106 |
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| DOID:0060041 | autism spectrum disorder | HGNC:23022 | Homo sapiens (human) | 140883 | ZNF280B |
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| DOID:1059 | intellectual disability | HGNC:23022 | Homo sapiens (human) | 140883 | ZNF280B |
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| DOID:0060041 | autism spectrum disorder | HGNC:25953 | Homo sapiens (human) | 54816 | ZNF280D |
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| DOID:1059 | intellectual disability | HGNC:25953 | Homo sapiens (human) | 54816 | ZNF280D |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18410 | Homo sapiens (human) | 23036 | ZNF292 |
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| DOID:0070294 | primary autosomal recessive microcephaly 10 | HGNC:15807 | Homo sapiens (human) | 63925 | ZNF335 |
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| DOID:2786 | cerebellar disease | HGNC:16762 | Homo sapiens (human) | 23090 | ZNF423 |
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| DOID:2785 | Dandy-Walker syndrome | HGNC:16762 | Homo sapiens (human) | 23090 | ZNF423 |
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| DOID:0111122 | nephronophthisis 14 | HGNC:16762 | Homo sapiens (human) | 23090 | ZNF423 |
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| DOID:14320 | generalized anxiety disorder | HGNC:21684 | Homo sapiens (human) | 58499 | ZNF462 |
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| DOID:5419 | schizophrenia | HGNC:24605 | Homo sapiens (human) | 25925 | ZNF521 |
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| DOID:11830 | myopia | HGNC:29222 | Homo sapiens (human) | 84146 | ZNF644 |
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| DOID:0081369 | Paget's disease of bone 6 | HGNC:29277 | Homo sapiens (human) | 57592 | ZNF687 |
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| DOID:612 | primary immunodeficiency disease | HGNC:29271 | Homo sapiens (human) | 57169 | ZNFX1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:23019 | Homo sapiens (human) | 8233 | ZRSR2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:23019 | Homo sapiens (human) | 8233 | ZRSR2 |
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| DOID:0060342 | acromelic frontonasal dysostosis | HGNC:29316 | Homo sapiens (human) | 57688 | ZSWIM6 |
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