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:4608 | common bile duct neoplasm | FB:FBgn0051115 | Drosophila melanogaster (fruit fly) | 318597 | CG31115 |
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DOID:4608 | common bile duct neoplasm | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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DOID:4608 | common bile duct neoplasm | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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DOID:4608 | common bile duct neoplasm | ZFIN:ZDB-GENE-040426-1505 | Danio rerio (zebrafish) | 393526 | mtap |
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DOID:10459 | common cold | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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DOID:12177 | common variable immunodeficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:0050811 | congenital adrenal hyperplasia | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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DOID:0050811 | congenital adrenal hyperplasia | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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DOID:0050811 | congenital adrenal hyperplasia | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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DOID:0050811 | congenital adrenal hyperplasia | HGNC:2600 | Homo sapiens (human) | 1589 | CYP21A2 |
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DOID:0050811 | congenital adrenal hyperplasia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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DOID:0050546 | congenital adrenal insufficiency | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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DOID:0111069 | congenital bile acid synthesis defect 2 | SGD:S000005646 | Saccharomyces cerevisiae S288C | 854287 | GCY1 |
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DOID:0111069 | congenital bile acid synthesis defect 2 | HGNC:388 | Homo sapiens (human) | 6718 | AKR1D1 |
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DOID:0111069 | congenital bile acid synthesis defect 2 | SGD:S000002776 | Saccharomyces cerevisiae S288C | 851974 | YPR1 |
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DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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DOID:3827 | congenital diaphragmatic hernia | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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DOID:3827 | congenital diaphragmatic hernia | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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DOID:3827 | congenital diaphragmatic hernia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:3827 | congenital diaphragmatic hernia | RGD:69303 | Rattus norvegicus (Norway rat) | 29633 | Ndst1 |
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DOID:3827 | congenital diaphragmatic hernia | RGD:2870 | Rattus norvegicus (Norway rat) | 24483 | Igf2 |
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DOID:3827 | congenital diaphragmatic hernia | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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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