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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
GlycoPOST
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:0110927 | nemaline myopathy 3 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:13832 | patent ductus arteriosus | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:10486 | intestinal atresia | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:13099 | Moyamoya disease | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081340 | congenital myopathy 2C | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081339 | congenital myopathy 2B | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:0050567 | orofacial cleft | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:11981 | morbid obesity | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:1574 | alcohol use disorder | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:9282 | ocular hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:10763 | hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:8577 | ulcerative colitis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:10825 | essential hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:9119 | acute myeloid leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:1240 | leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:1059 | intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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