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:0050742 | nicotine dependence | WB:WBGene00021528 | Caenorhabditis elegans | 189837 | gbb-1 |
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DOID:670 | amphetamine abuse | WB:WBGene00021528 | Caenorhabditis elegans | 189837 | gbb-1 |
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DOID:0050741 | alcohol dependence | WB:WBGene00021528 | Caenorhabditis elegans | 189837 | gbb-1 |
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DOID:11832 | visual epilepsy | WB:WBGene00021528 | Caenorhabditis elegans | 189837 | gbb-1 |
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DOID:10763 | hypertension | WB:WBGene00021528 | Caenorhabditis elegans | 189837 | gbb-1 |
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DOID:3211 | lysosomal storage disease | WB:WBGene00021546 | Caenorhabditis elegans | 3565323 | laat-1 |
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DOID:8454 | riboflavin deficiency | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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DOID:0050694 | Brown-Vialetto-Van Laere syndrome | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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DOID:0080786 | Brown-Vialetto-Van Laere syndrome 2 | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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DOID:0080785 | Brown-Vialetto-Van Laere syndrome 1 | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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DOID:0080632 | Fazio-Londe disease | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | WB:WBGene00021840 | Caenorhabditis elegans | 171881 | pign-1 |
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DOID:4621 | holoprosencephaly | WB:WBGene00021840 | Caenorhabditis elegans | 171881 | pign-1 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:12930 | dilated cardiomyopathy | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:12387 | nephrogenic diabetes insipidus | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:10534 | stomach cancer | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:3908 | lung non-small cell carcinoma | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:9253 | gastrointestinal stromal tumor | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:936 | brain disease | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:1324 | lung cancer | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:0111970 | immunodeficiency 10 | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:0080089 | tubular aggregate myopathy 1 | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:9970 | obesity | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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DOID:0060354 | Stormorken syndrome | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-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