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:0060292 | X-linked chondrodysplasia punctata 1 | MGI:107822 | Mus musculus (house mouse) | 13595 | Ebp |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:719 | Homo sapiens (human) | 415 | ARSL |
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DOID:0060291 | oculodentodigital dysplasia | MGI:95713 | Mus musculus (house mouse) | 14609 | Gja1 |
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DOID:0060290 | Ohdo syndrome, SBBYS variant | FB:FBgn0034975 | Drosophila melanogaster (fruit fly) | 37859 | enok |
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DOID:0060290 | Ohdo syndrome, SBBYS variant | MGI:1858746 | Mus musculus (house mouse) | 54169 | Kat6b |
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DOID:0060290 | Ohdo syndrome, SBBYS variant | HGNC:17582 | Homo sapiens (human) | 23522 | KAT6B |
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DOID:0060287 | cornea plana | ZFIN:ZDB-GENE-041210-165 | Danio rerio (zebrafish) | 567017 | kera |
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DOID:0060287 | cornea plana | MGI:1202398 | Mus musculus (house mouse) | 16545 | Kera |
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DOID:0060287 | cornea plana | HGNC:6309 | Homo sapiens (human) | 11081 | KERA |
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DOID:0060287 | cornea plana | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:26223 | Homo sapiens (human) | 79736 | TEFM |
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DOID:0060286 | combined oxidative phosphorylation deficiency | MGI:1915541 | Mus musculus (house mouse) | 68291 | Mto1 |
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DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:19261 | Homo sapiens (human) | 25821 | MTO1 |
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DOID:0060285 | parietal foramina | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | WB:WBGene00008918 | Caenorhabditis elegans | 179519 | pigt-1 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | RGD:2232 | Rattus norvegicus (Norway rat) | 24232 | C3 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | Xenbase:XB-GENE-489917 | Xenopus tropicalis (tropical clawed frog) | 100038176 | cxcr4 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | Xenbase:XB-GENE-489921 | Xenopus laevis (African clawed frog) | 100192360 | cxcr4.L |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | Xenbase:XB-GENE-6256540 | Xenopus laevis (African clawed frog) | 380373 | cxcr4.S |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | RGD:620465 | Rattus norvegicus (Norway rat) | 60628 | Cxcr4 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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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