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:0060572 | Ritscher-Schinzel syndrome 2 | HGNC:28909 | Homo sapiens (human) | 28952 | CCDC22 |
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DOID:12347 | osteogenesis imperfecta | HGNC:26185 | Homo sapiens (human) | 79879 | CCDC134 |
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DOID:1324 | lung cancer | HGNC:26688 | Homo sapiens (human) | 164592 | CCDC116 |
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DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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DOID:0060366 | Hennekam syndrome | HGNC:29426 | Homo sapiens (human) | 147372 | CCBE1 |
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DOID:7148 | rheumatoid arthritis | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:2560 | morphine dependence | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:12716 | newborn respiratory distress syndrome | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:0050589 | inflammatory bowel disease | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:535 | sleep disorder | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:2841 | asthma | FB:FBgn0039396 | Drosophila melanogaster (fruit fly) | 2768688 | CCAP-R |
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DOID:0060340 | ciliopathy | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:0111004 | Joubert syndrome 9 | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:10584 | retinitis pigmentosa | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:0050778 | Meckel syndrome | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:0050545 | visceral heterotaxy | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:0050777 | Joubert syndrome | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:0070120 | Meckel syndrome 6 | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:1059 | intellectual disability | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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DOID:1059 | intellectual disability | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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DOID:0081179 | autosomal recessive intellectual developmental disorder 3 | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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DOID:0050545 | visceral heterotaxy | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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DOID:0060340 | ciliopathy | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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DOID:162 | cancer | HGNC:15962 | Homo sapiens (human) | 57332 | CBX8 |
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DOID:3068 | glioblastoma | HGNC:15962 | Homo sapiens (human) | 57332 | CBX8 |
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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