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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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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:0080108 | myoglobinuria | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:9970 | obesity | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0080108 | myoglobinuria | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0050453 | lissencephaly | HGNC:14434 | Homo sapiens (human) | 65061 | CDK15 |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:14430 | Homo sapiens (human) | 64849 | SLC13A3 |
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| DOID:0050667 | alcohol-related neurodevelopmental disorder | HGNC:14430 | Homo sapiens (human) | 64849 | SLC13A3 |
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| DOID:1826 | epilepsy | HGNC:14430 | Homo sapiens (human) | 64849 | SLC13A3 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:2566 | corneal dystrophy | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:1508 | candidiasis | HGNC:14410 | Homo sapiens (human) | 170506 | DHX36 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:1441 | Homo sapiens (human) | 800 | CALD1 |
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| DOID:655 | inherited metabolic disorder | HGNC:14409 | Homo sapiens (human) | 60386 | SLC25A19 |
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| DOID:10907 | microcephaly | HGNC:14409 | Homo sapiens (human) | 60386 | SLC25A19 |
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| DOID:14330 | Parkinson's disease | HGNC:14402 | Homo sapiens (human) | 28996 | HIPK2 |
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| DOID:11476 | osteoporosis | HGNC:1440 | Homo sapiens (human) | 799 | CALCR |
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| DOID:10486 | intestinal atresia | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:13832 | patent ductus arteriosus | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:0081113 | Baraitser-Winter syndrome 2 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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