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 |
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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 |
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DOID:0050338 | primary bacterial infectious disease | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:1459 | hypothyroidism | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:0112189 | thyroid dyshormonogenesis 6 | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:0050328 | congenital hypothyroidism | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:8577 | ulcerative colitis | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:28 | endocrine system disease | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-4 |
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DOID:2377 | multiple sclerosis | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-4 |
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DOID:0070256 | congenital disorder of glycosylation type IId | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-4 |
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DOID:2986 | IgA glomerulonephritis | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-4 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-4 |
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DOID:1793 | pancreatic cancer | WB:WBGene00000270 | Caenorhabditis elegans | 178142 | bre-5 |
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DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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DOID:0110969 | brachydactyly type B1 | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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DOID:674 | cleft palate | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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DOID:0060764 | autosomal recessive Robinow syndrome | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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DOID:14175 | von Hippel-Lindau disease | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:3602 | toxic encephalopathy | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:809 | cocaine abuse | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:5419 | schizophrenia | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:670 | amphetamine abuse | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:14330 | Parkinson's disease | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:1440 | Machado-Joseph disease | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:3312 | bipolar disorder | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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DOID:0070490 | infantile parkinsonism-dystonia 2 | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024