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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:12930 | dilated cardiomyopathy | HGNC:6189 | Homo sapiens (human) | 3714 | JAG2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:6189 | Homo sapiens (human) | 3714 | JAG2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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||
| DOID:11714 | gestational diabetes | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:10591 | pre-eclampsia | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:9970 | obesity | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:9970 | obesity | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:11714 | gestational diabetes | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:10591 | pre-eclampsia | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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||
| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:0060603 | isolated anhidrosis with normal sweat glands | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:0050965 | spinocerebellar ataxia type 15 | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:224 | transient cerebral ischemia | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:1682 | congenital heart disease | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:0111578 | Gillespie syndrome | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:12858 | Huntington's disease | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:0050978 | spinocerebellar ataxia type 29 | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:0060319 | cardiac arrest | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:10591 | pre-eclampsia | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
|
