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:0060668 | anencephaly | HGNC:29558 | Homo sapiens (human) | 81788 | NUAK2 |
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DOID:0060668 | anencephaly | SGD:S000002529 | Saccharomyces cerevisiae S288C | 851700 | KIN1 |
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DOID:0060668 | anencephaly | WB:WBGene00001165 | Caenorhabditis elegans | 176882 | efn-4 |
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DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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DOID:0060668 | anencephaly | SGD:S000004086 | Saccharomyces cerevisiae S288C | 850785 | KIN2 |
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DOID:0060668 | anencephaly | RGD:620391 | Rattus norvegicus (Norway rat) | 116683 | Efna5 |
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DOID:0060668 | anencephaly | ZFIN:ZDB-GENE-980526-186 | Danio rerio (zebrafish) | 30223 | efna5b |
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DOID:0060656 | autosomal recessive congenital ichthyosis 1 | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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DOID:0060656 | autosomal recessive congenital ichthyosis 1 | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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DOID:0060656 | autosomal recessive congenital ichthyosis 1 | MGI:2676312 | Mus musculus (house mouse) | 74591 | Abca12 |
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DOID:0060654 | lethal congenital contracture syndrome 4 | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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DOID:0060653 | lethal congenital contracture syndrome 3 | MGI:1298224 | Mus musculus (house mouse) | 18717 | Pip5k1c |
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DOID:0060652 | familial erythrocytosis 1 | HGNC:3416 | Homo sapiens (human) | 2057 | EPOR |
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DOID:0060652 | familial erythrocytosis 1 | MGI:95408 | Mus musculus (house mouse) | 13857 | Epor |
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DOID:0060652 | familial erythrocytosis 1 | Xenbase:XB-GENE-6251686 | Xenopus laevis (African clawed frog) | 734211 | epor.L |
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DOID:0060651 | MYH-9 related disease | MGI:107717 | Mus musculus (house mouse) | 17886 | Myh9 |
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DOID:0060651 | MYH-9 related disease | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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DOID:0060650 | dicarboxylic aminoaciduria | RGD:3696 | Rattus norvegicus (Norway rat) | 25550 | Slc1a1 |
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DOID:0060650 | dicarboxylic aminoaciduria | MGI:105083 | Mus musculus (house mouse) | 20510 | Slc1a1 |
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DOID:0060650 | dicarboxylic aminoaciduria | WB:WBGene00001622 | Caenorhabditis elegans | 188744 | glt-4 |
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DOID:0060650 | dicarboxylic aminoaciduria | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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DOID:0060649 | congenital hereditary endothelial dystrophy of cornea | MGI:2138987 | Mus musculus (house mouse) | 269356 | Slc4a11 |
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DOID:0060649 | congenital hereditary endothelial dystrophy of cornea | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
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DOID:0060648 | anterior segment dysgenesis | MGI:1929183 | Mus musculus (house mouse) | 64930 | Tsc1 |
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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