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:3905 | lung carcinoma | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:1470 | major depressive disorder | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:0050742 | nicotine dependence | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:0050741 | alcohol dependence | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:9256 | colorectal cancer | WB:WBGene00006776 | Caenorhabditis elegans | 172233 | unc-40 |
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DOID:3748 | esophagus squamous cell carcinoma | WB:WBGene00006776 | Caenorhabditis elegans | 172233 | unc-40 |
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DOID:0111153 | congenital mirror movement disorder | WB:WBGene00006776 | Caenorhabditis elegans | 172233 | unc-40 |
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DOID:0112202 | developmental and epileptic encephalopathy | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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DOID:0060170 | generalized epilepsy with febrile seizures plus | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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DOID:3328 | temporal lobe epilepsy | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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DOID:1574 | alcohol use disorder | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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DOID:0090005 | Schwartz-Jampel syndrome 1 | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:2256 | osteochondrodysplasia | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:4195 | hyperglycemia | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:13481 | thanatophoric dysplasia | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:10763 | hypertension | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:0060770 | dextro-looped transposition of the great arteries | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:3407 | carotid artery disease | WB:WBGene00006787 | Caenorhabditis elegans | 175126 | unc-52 |
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DOID:3312 | bipolar disorder | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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DOID:11832 | visual epilepsy | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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DOID:0060682 | autosomal dominant nocturnal frontal lobe epilepsy 1 | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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DOID:0110679 | congenital myasthenic syndrome 4C | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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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