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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:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:11133 | Homo sapiens (human) | 9342 | SNAP29 |
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| DOID:0080196 | mandibulofacial dysostosis, Guion-Almeida type | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:10485 | esophageal atresia | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:10907 | microcephaly | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:2908 | Treacher Collins syndrome | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:2043 | hepatitis B | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:16835 | Homo sapiens (human) | 9344 | TAOK2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:16835 | Homo sapiens (human) | 9344 | TAOK2 |
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| DOID:162 | cancer | HGNC:16835 | Homo sapiens (human) | 9344 | TAOK2 |
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| DOID:331 | central nervous system disease | HGNC:16835 | Homo sapiens (human) | 9344 | TAOK2 |
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| DOID:14227 | azoospermia | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:1059 | intellectual disability | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:0050144 | Kartagener syndrome | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:0050545 | visceral heterotaxy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:0060224 | atrial fibrillation | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:2975 | cystic kidney disease | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:8947 | diabetic retinopathy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:224 | transient cerebral ischemia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:0080745 | polymyositis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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