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 | July 29, 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:0050636 | familial visceral amyloidosis | FB:FBgn0004427 | Drosophila melanogaster (fruit fly) | 38127 | LysD | CG9118 |
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DOID:0050642 | hypochromic microcytic anemia | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050642 | hypochromic microcytic anemia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0050642 | hypochromic microcytic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0050644 | arterial calcification of infancy | MGI:97370 | Mus musculus (house mouse) | 18605 | Enpp1 |
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DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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DOID:0050644 | arterial calcification of infancy | RGD:628825 | Rattus norvegicus (Norway rat) | 85496 | Enpp1 |
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DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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DOID:0050647 | Arts syndrome | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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DOID:0050648 | atelosteogenesis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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DOID:0050650 | familial atrial fibrillation | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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DOID:0050650 | familial atrial fibrillation | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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DOID:0050650 | familial atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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DOID:0050663 | Bethlem myopathy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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DOID:0050665 | fetal alcohol syndrome | SGD:S000006369 | Saccharomyces cerevisiae S288C | 856294 | RHO1 |
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DOID:0050669 | spastic cerebral palsy | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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DOID:0050669 | spastic cerebral palsy | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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DOID:0050685 | small cell carcinoma | FB:FBgn0026415 | Drosophila melanogaster (fruit fly) | 31926 | Idgf4 | CG1780 |
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DOID:0050685 | small cell carcinoma | FB:FBgn0013763 | Drosophila melanogaster (fruit fly) | 36868 | Idgf6 |
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DOID:0050685 | small cell carcinoma | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050685 | small cell carcinoma | MGI:1340899 | Mus musculus (house mouse) | 12654 | Chi3l1 |
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DOID:0050685 | small cell carcinoma | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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DOID:0050685 | small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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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 v4.0.0
Last updated: August 19, 2024