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:0050453 | lissencephaly | Xenbase:XB-GENE-6489079 | Xenopus laevis (African clawed frog) | 108698684 | pomt2.L |
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DOID:0050453 | lissencephaly | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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DOID:0050453 | lissencephaly | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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DOID:0050452 | mevalonic aciduria | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0050452 | mevalonic aciduria | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050452 | mevalonic aciduria | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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DOID:0050432 | Asperger syndrome | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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DOID:0050432 | Asperger syndrome | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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DOID:0050426 | Stevens-Johnson syndrome | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050426 | Stevens-Johnson syndrome | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0050426 | Stevens-Johnson syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0050424 | familial adenomatous polyposis | MGI:1917853 | Mus musculus (house mouse) | 70603 | Mutyh |
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DOID:0050424 | familial adenomatous polyposis | RGD:620045 | Rattus norvegicus (Norway rat) | 170841 | Mutyh |
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DOID:0050424 | familial adenomatous polyposis | FB:FBgn0026597 | Drosophila melanogaster (fruit fly) | 43565 | Axn |
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DOID:0050424 | familial adenomatous polyposis | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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DOID:0050424 | familial adenomatous polyposis | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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DOID:0050328 | congenital hypothyroidism | FB:FBgn0004057 | Drosophila melanogaster (fruit fly) | 32974 | Zw |
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DOID:0050328 | congenital hypothyroidism | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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DOID:0050328 | congenital hypothyroidism | MGI:105977 | Mus musculus (house mouse) | 14380 | G6pd2 |
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DOID:0050328 | congenital hypothyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:0050328 | congenital hypothyroidism | MGI:105979 | Mus musculus (house mouse) | 14381 | G6pdx |
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DOID:0050328 | congenital hypothyroidism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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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