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:12849 | autistic disorder | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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DOID:0060350 | adenine phosphoribosyltransferase deficiency | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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DOID:1793 | pancreatic cancer | FB:FBgn0039378 | Drosophila melanogaster (fruit fly) | 43124 | alpha4GT2 | CG5878 |
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DOID:1793 | pancreatic cancer | FB:FBgn0031491 | Drosophila melanogaster (fruit fly) | 33512 | alpha4GT1 | CG17223 |
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DOID:0081097 | Rafiq syndrome | FB:FBgn0039634 | Drosophila melanogaster (fruit fly) | 43436 | alpha-Man-Ib | CG11874 |
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DOID:1338 | congenital dyserythropoietic anemia | FB:FBgn0011740 | Drosophila melanogaster (fruit fly) | 41126 | alpha-Man-IIa | CG18802 |
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DOID:5419 | schizophrenia | FB:FBgn0011740 | Drosophila melanogaster (fruit fly) | 41126 | alpha-Man-IIa | CG18802 |
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DOID:9074 | systemic lupus erythematosus | FB:FBgn0011740 | Drosophila melanogaster (fruit fly) | 41126 | alpha-Man-IIa | CG18802 |
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DOID:0080564 | congenital disorder of glycosylation Il | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0050770 | polycystic liver disease | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0080560 | congenital disorder of glycosylation Ih | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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DOID:0080562 | congenital disorder of glycosylation Ij | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0110676 | congenital myasthenic syndrome 13 | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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DOID:0080555 | congenital disorder of glycosylation Ic | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:0080322 | polycystic kidney disease | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:0080556 | congenital disorder of glycosylation Id | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:0110669 | congenital myasthenic syndrome 14 | WB:WBGene00017282 | Caenorhabditis elegans | 173912 | algn-2 |
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DOID:0080561 | congenital disorder of glycosylation Ii | WB:WBGene00017282 | Caenorhabditis elegans | 173912 | algn-2 |
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DOID:0110658 | congenital myasthenic syndrome 15 | WB:WBGene00019725 | Caenorhabditis elegans | 187398 | algn-14 |
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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