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:6000 | congestive heart failure | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:0080199 | colorectal carcinoma | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:5844 | myocardial infarction | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:7148 | rheumatoid arthritis | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:1612 | breast cancer | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:3083 | chronic obstructive pulmonary disease | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:0050127 | sinusitis | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:9538 | multiple myeloma | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:1380 | endometrial cancer | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:10003 | sensorineural hearing loss | WB:WBGene00018037 | Caenorhabditis elegans | 180809 | chtl-1 |
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DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | WB:WBGene00018037 | Caenorhabditis elegans | 180809 | chtl-1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | WB:WBGene00006477 | Caenorhabditis elegans | 181125 | chup-1 |
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DOID:0110144 | Bartter disease type 3 | Xenbase:XB-GENE-6252397 | Xenopus laevis (African clawed frog) | 378616 | clcnkb.L |
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DOID:0110146 | Bartter disease type 4b | Xenbase:XB-GENE-6252397 | Xenopus laevis (African clawed frog) | 378616 | clcnkb.L |
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DOID:0050450 | Gitelman syndrome | Xenbase:XB-GENE-6252397 | Xenopus laevis (African clawed frog) | 378616 | clcnkb.L |
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DOID:10763 | hypertension | Xenbase:XB-GENE-6252397 | Xenopus laevis (African clawed frog) | 378616 | clcnkb.L |
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DOID:10808 | gastric ulcer | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:423 | myopathy | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:0050700 | cardiomyopathy | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:12930 | dilated cardiomyopathy | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:8577 | ulcerative colitis | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:0060680 | pigment dispersion syndrome | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-1 |
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DOID:1405 | primary angle-closure glaucoma | WB:WBGene00000527 | Caenorhabditis elegans | 172678 | cle-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