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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
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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:10588 | adrenoleukodystrophy | HGNC:24174 | Homo sapiens (human) | 81616 | ACSBG2 |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:12798 | mucopolysaccharidosis | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:9870 | galactosemia | HGNC:24063 | Homo sapiens (human) | 130589 | GALM |
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| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:23792 | Homo sapiens (human) | 122618 | PLD4 |
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| DOID:162 | cancer | HGNC:23786 | Homo sapiens (human) | 79837 | PIP4K2C |
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| DOID:8778 | Crohn's disease | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
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| DOID:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0050589 | inflammatory bowel disease | HGNC:23614 | Homo sapiens (human) | 55808 | ST6GALNAC1 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:1612 | breast cancer | HGNC:23531 | Homo sapiens (human) | 196051 | PLPP4 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:4194 | glucose metabolism disease | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:4195 | hyperglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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