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:0081292 | traumatic brain injury | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:83 | cataract | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:0050700 | cardiomyopathy | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:0060258 | reticulate acropigmentation of Kitamura | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:14004 | thoracic aortic aneurysm | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:0110050 | Alzheimer's disease 18 | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:1824 | status epilepticus | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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DOID:13096 | Sneddon syndrome | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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DOID:2957 | pulmonary tuberculosis | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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DOID:106 | pleural tuberculosis | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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DOID:6432 | pulmonary hypertension | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:224 | transient cerebral ischemia | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:11294 | arteriovenous malformation | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:13374 | fibrodysplasia ossificans progressiva | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:0060688 | arteriovenous malformations of the brain | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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DOID:0060856 | right atrial isomerism | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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DOID:14323 | Marfan syndrome | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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DOID:0050787 | juvenile polyposis syndrome | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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DOID:10591 | pre-eclampsia | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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DOID:0050545 | visceral heterotaxy | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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DOID:1793 | pancreatic cancer | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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DOID:14323 | Marfan syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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DOID:3883 | Lynch syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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DOID:4258 | Weissenbacher-Zweymuller syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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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