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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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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:0050453 | lissencephaly | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:9884 | muscular dystrophy | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0060264 | pontocerebellar hypoplasia | MGI:1915526 | Mus musculus (house mouse) | 68276 | Toe1 |
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| DOID:0060276 | pontocerebellar hypoplasia type 7 | MGI:1915526 | Mus musculus (house mouse) | 68276 | Toe1 |
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| DOID:0111480 | combined oxidative phosphorylation deficiency 10 | MGI:1915541 | Mus musculus (house mouse) | 68291 | Mto1 |
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| DOID:0060286 | combined oxidative phosphorylation deficiency | MGI:1915541 | Mus musculus (house mouse) | 68291 | Mto1 |
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| DOID:0050563 | nonsyndromic deafness | MGI:1915541 | Mus musculus (house mouse) | 68291 | Mto1 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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| DOID:0080572 | congenital disorder of glycosylation Iw | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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| DOID:14452 | hypokalemic periodic paralysis | RGD:70983 | Rattus norvegicus (Norway rat) | 682930 | Cacna1s |
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| DOID:8545 | malignant hyperthermia | RGD:70983 | Rattus norvegicus (Norway rat) | 682930 | Cacna1s |
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| DOID:0081350 | congenital myopathy 18 | RGD:70983 | Rattus norvegicus (Norway rat) | 682930 | Cacna1s |
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| DOID:0060173 | Timothy syndrome | RGD:70983 | Rattus norvegicus (Norway rat) | 682930 | Cacna1s |
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| DOID:11723 | Duchenne muscular dystrophy | RGD:70983 | Rattus norvegicus (Norway rat) | 682930 | Cacna1s |
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| DOID:225 | syndrome | MGI:1915566 | Mus musculus (house mouse) | 68316 | Apoo |
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| DOID:4724 | brain edema | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0060319 | cardiac arrest | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0060334 | transient neonatal diabetes mellitus | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:10763 | hypertension | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:9993 | hypoglycemia | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0112262 | leucine-sensitive hypoglycemia of infancy | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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