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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:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:162 | cancer | HGNC:30596 | Homo sapiens (human) | 80235 | PIGZ |
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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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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:4621 | holoprosencephaly | HGNC:25712 | Homo sapiens (human) | 80055 | PGAP1 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:26292 | Homo sapiens (human) | 79993 | ELOVL7 |
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| DOID:0050589 | inflammatory bowel disease | ZFIN:ZDB-GENE-041014-161 | Danio rerio (zebrafish) | 799868 | st6galnac1.2 |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0080201 | Peters plus syndrome | ZFIN:ZDB-GENE-110411-147 | Danio rerio (zebrafish) | 799443 | b3glcta |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050574 | L-2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:10283 | prostate cancer | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:104 | bacterial infectious disease | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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