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:684 | hepatocellular carcinoma | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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DOID:1184 | nephrotic syndrome | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:9406 | hypopituitarism | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:224 | transient cerebral ischemia | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:162 | cancer | SGD:S000005675 | Saccharomyces cerevisiae S288C | 854320 | SMP3 |
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DOID:1059 | intellectual disability | FB:FBgn0015615 | Drosophila melanogaster (fruit fly) | 32627 | SMC3 |
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DOID:1059 | intellectual disability | SGD:S000003610 | Saccharomyces cerevisiae S288C | 853371 | SMC3 |
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DOID:11725 | Cornelia de Lange syndrome | FB:FBgn0015615 | Drosophila melanogaster (fruit fly) | 32627 | SMC3 |
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DOID:0080507 | Cornelia de Lange syndrome 3 | SGD:S000003610 | Saccharomyces cerevisiae S288C | 853371 | SMC3 |
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DOID:684 | hepatocellular carcinoma | SGD:S000003610 | Saccharomyces cerevisiae S288C | 853371 | SMC3 |
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DOID:11725 | Cornelia de Lange syndrome | SGD:S000003610 | Saccharomyces cerevisiae S288C | 853371 | SMC3 |
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DOID:0080507 | Cornelia de Lange syndrome 3 | FB:FBgn0015615 | Drosophila melanogaster (fruit fly) | 32627 | SMC3 |
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DOID:11725 | Cornelia de Lange syndrome | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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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