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:0112233 | lissencephaly 8 | ZFIN:ZDB-GENE-061221-2 | Danio rerio (zebrafish) | 100150181 | tmtc3 |
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DOID:3146 | lipid metabolism disorder | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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DOID:3459 | breast carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:9993 | hypoglycemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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DOID:2349 | arteriosclerosis | MGI:104993 | Mus musculus (house mouse) | 16847 | Lepr |
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DOID:3748 | esophagus squamous cell carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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DOID:3393 | coronary artery disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:11476 | osteoporosis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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DOID:3525 | middle cerebral artery infarction | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0050771 | pheochromocytoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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DOID:0050559 | Fukuyama congenital muscular dystrophy | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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DOID:2394 | ovarian cancer | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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DOID:4194 | glucose metabolism disease | MGI:1341295 | Mus musculus (house mouse) | 21897 | Tlr1 |
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DOID:4195 | hyperglycemia | MGI:96759 | Mus musculus (house mouse) | 16828 | Ldha |
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DOID:5199 | ureteral obstruction | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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DOID:0111673 | Saul-Wilson syndrome | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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DOID:0050866 | oral squamous cell carcinoma | WB:WBGene00001686 | Caenorhabditis elegans | 174578 | gpd-4 |
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DOID:1074 | kidney failure | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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DOID:9352 | type 2 diabetes mellitus | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:850 | lung disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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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