Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0081326 | oxoglutarate dehydrogenase deficiency | MGI:1098267 | Mus musculus (house mouse) | 18293 | Ogdh |
|
||
| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
|
||
| DOID:0081326 | oxoglutarate dehydrogenase deficiency | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
|
||
| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
|
||
| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
|
||
| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
|
||
| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | MGI:98266 | Mus musculus (house mouse) | 20322 | Sord |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | RGD:3734 | Rattus norvegicus (Norway rat) | 24788 | Sord |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | SGD:S000004060 | Saccharomyces cerevisiae S288C | 850759 | XYL2 |
|
||
| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
|
||
| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
|
||
| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | RGD:3269 | Rattus norvegicus (Norway rat) | 25737 | Pcna |
|
||
| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | MGI:97503 | Mus musculus (house mouse) | 18538 | Pcna |
|
||
| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
|
||
| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | RGD:3734 | Rattus norvegicus (Norway rat) | 24788 | Sord |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000004060 | Saccharomyces cerevisiae S288C | 850759 | XYL2 |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | MGI:98266 | Mus musculus (house mouse) | 20322 | Sord |
|
||
| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
|
||
| DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
|
