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:0050127 | sinusitis | MGI:1932052 | Mus musculus (house mouse) | 81600 | Chia1 |
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DOID:12053 | cryptococcosis | MGI:1932052 | Mus musculus (house mouse) | 81600 | Chia1 |
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DOID:10325 | silicosis | MGI:1932052 | Mus musculus (house mouse) | 81600 | Chia1 |
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DOID:10588 | adrenoleukodystrophy | HGNC:24174 | Homo sapiens (human) | 81616 | ACSBG2 |
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DOID:3649 | pyruvate decarboxylase deficiency | RGD:619859 | Rattus norvegicus (Norway rat) | 81654 | Dlat |
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DOID:3650 | lactic acidosis | RGD:619859 | Rattus norvegicus (Norway rat) | 81654 | Dlat |
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DOID:2747 | glycogen storage disease | RGD:621785 | Rattus norvegicus (Norway rat) | 81675 | Gyg1 |
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DOID:0050579 | glycogen storage disease XV | RGD:621785 | Rattus norvegicus (Norway rat) | 81675 | Gyg1 |
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DOID:2841 | asthma | HGNC:15634 | Homo sapiens (human) | 81793 | TLR10 |
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DOID:6000 | congestive heart failure | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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DOID:2316 | brain ischemia | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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DOID:5844 | myocardial infarction | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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DOID:0080433 | developmental and epileptic encephalopathy 51 | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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DOID:9970 | obesity | HGNC:1473 | Homo sapiens (human) | 821 | CANX |
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DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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DOID:557 | kidney disease | MGI:1932466 | Mus musculus (house mouse) | 83379 | Klb |
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DOID:0060041 | autism spectrum disorder | MGI:1932544 | Mus musculus (house mouse) | 83398 | Ndst3 |
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DOID:1059 | intellectual disability | MGI:1932544 | Mus musculus (house mouse) | 83398 | Ndst3 |
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DOID:14227 | azoospermia | MGI:1932544 | Mus musculus (house mouse) | 83398 | Ndst3 |
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DOID:12466 | secondary hyperparathyroidism | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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DOID:9352 | type 2 diabetes mellitus | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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DOID:784 | chronic kidney disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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DOID:10584 | retinitis pigmentosa | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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DOID:3393 | coronary artery disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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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