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:2957 | pulmonary tuberculosis | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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DOID:1824 | status epilepticus | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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DOID:13359 | Ehlers-Danlos syndrome | HGNC:11976 | Homo sapiens (human) | 7148 | TNXB |
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DOID:0060564 | spinal disease | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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DOID:12177 | common variable immunodeficiency | HGNC:5351 | Homo sapiens (human) | 29851 | ICOS |
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DOID:10325 | silicosis | HGNC:6319 | Homo sapiens (human) | 11127 | KIF3A |
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DOID:4448 | macular degeneration | MGI:105384 | Mus musculus (house mouse) | 15481 | Hspa8 |
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DOID:1289 | neurodegenerative disease | HGNC:16703 | Homo sapiens (human) | 57084 | SLC17A6 |
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DOID:11832 | visual epilepsy | HGNC:13447 | Homo sapiens (human) | 81539 | SLC38A1 |
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DOID:289 | endometriosis | MGI:95669 | Mus musculus (house mouse) | 14473 | Gc |
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DOID:14766 | renal agenesis | Xenbase:XB-GENE-1013855 | Xenopus tropicalis (tropical clawed frog) | 100125202 | gfra1 |
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DOID:1883 | hepatitis C | RGD:68949 | Rattus norvegicus (Norway rat) | 116553 | Il13 |
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DOID:127 | leiomyoma | HGNC:3685 | Homo sapiens (human) | 2252 | FGF7 |
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DOID:13099 | Moyamoya disease | MGI:87909 | Mus musculus (house mouse) | 11475 | Acta2 |
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DOID:14323 | Marfan syndrome | WB:WBGene00022816 | Caenorhabditis elegans | 176076 | fbn-1 |
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DOID:1561 | cognitive disorder | MGI:99841 | Mus musculus (house mouse) | 15566 | Htr7 |
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DOID:2048 | autoimmune hepatitis | RGD:620047 | Rattus norvegicus (Norway rat) | 116562 | Il2 |
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DOID:10652 | Alzheimer's disease | RGD:619993 | Rattus norvegicus (Norway rat) | 65262 | Atp5f1a |
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DOID:0090109 | autosomal dominant hypocalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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DOID:557 | kidney disease | MGI:1314884 | Mus musculus (house mouse) | 21937 | Tnfrsf1a |
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DOID:0080621 | glucocorticoid deficiency 1 | HGNC:6930 | Homo sapiens (human) | 4158 | MC2R |
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DOID:0050340 | opportunistic bacterial infectious disease | HGNC:11105 | Homo sapiens (human) | 6601 | SMARCC2 |
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DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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DOID:1852 | intrahepatic cholestasis | WB:WBGene00003995 | Caenorhabditis elegans | 178215 | pgp-1 |
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DOID:0112010 | pituitary adenoma 3 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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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