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GlyTouCan
Glycan Structure Repository
GlyComb
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:11476 | osteoporosis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:6364 | migraine | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:3525 | middle cerebral artery infarction | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:0080600 | COVID-19 | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:11716 | prediabetes syndrome | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:76 | stomach disease | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:0110982 | Joubert syndrome 13 | HGNC:26113 | Homo sapiens (human) | 79600 | TCTN1 |
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| DOID:1682 | congenital heart disease | HGNC:26164 | Homo sapiens (human) | 79612 | NAA16 |
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| DOID:1059 | intellectual disability | HGNC:26164 | Homo sapiens (human) | 79612 | NAA16 |
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| DOID:0060037 | developmental disorder of mental health | HGNC:26164 | Homo sapiens (human) | 79612 | NAA16 |
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| DOID:0060041 | autism spectrum disorder | HGNC:26164 | Homo sapiens (human) | 79612 | NAA16 |
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| DOID:0090070 | hypogonadotropic hypogonadism | HGNC:26256 | Homo sapiens (human) | 79625 | NDNF |
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| DOID:0060479 | Shwachman-Diamond syndrome | HGNC:25789 | Homo sapiens (human) | 79631 | EFL1 |
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| DOID:0060366 | Hennekam syndrome | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:0080586 | Van Maldergem syndrome 2 | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:1289 | neurodegenerative disease | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:305 | carcinoma | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:9970 | obesity | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:29478 | Homo sapiens (human) | 79641 | ROGDI |
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| DOID:1508 | candidiasis | ZFIN:ZDB-GENE-080723-75 | Danio rerio (zebrafish) | 796410 | fut9a |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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