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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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Repository for lectin-assisted multimodality data
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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:9970 | obesity | HGNC:17178 | Homo sapiens (human) | 80070 | ADAMTS20 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:17178 | Homo sapiens (human) | 80070 | ADAMTS20 |
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| DOID:0050545 | visceral heterotaxy | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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| DOID:2975 | cystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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| DOID:0111682 | diffuse cystic renal dysplasia | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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| DOID:3911 | progeria | HGNC:30897 | Homo sapiens (human) | 80124 | VCPIP1 |
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| DOID:4549 | extraskeletal myxoid chondrosarcoma | HGNC:7982 | Homo sapiens (human) | 8013 | NR4A3 |
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| DOID:0090001 | Fraser syndrome | HGNC:19185 | Homo sapiens (human) | 80144 | FRAS1 |
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| DOID:0111405 | Fraser syndrome 1 | HGNC:19185 | Homo sapiens (human) | 80144 | FRAS1 |
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| DOID:11836 | clubfoot | HGNC:19185 | Homo sapiens (human) | 80144 | FRAS1 |
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| DOID:0081213 | autosomal recessive intellectual developmental disorder 50 | HGNC:26114 | Homo sapiens (human) | 80153 | EDC3 |
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| DOID:1059 | intellectual disability | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:1682 | congenital heart disease | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:0080233 | autosomal dominant intellectual developmental disorder 50 | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:0060041 | autism spectrum disorder | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:0060037 | developmental disorder of mental health | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:1572 | normal pressure hydrocephalus | HGNC:26133 | Homo sapiens (human) | 80157 | CWH43 |
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| DOID:0050777 | Joubert syndrome | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0112352 | spermatogenic failure 58 | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0050545 | visceral heterotaxy | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0081011 | Bardet-Biedl syndrome 22 | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0080074 | neural tube defect | HGNC:26219 | Homo sapiens (human) | 80199 | FUZ |
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| DOID:11717 | neonatal diabetes | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
|
