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:1432 | blindness | SGD:S000005875 | Saccharomyces cerevisiae S288C | 854530 | PUT4 |
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DOID:0080855 | Parkinsonism | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:11832 | visual epilepsy | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:14115 | toxic shock syndrome | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:1712 | aortic valve stenosis | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:10763 | hypertension | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:10652 | Alzheimer's disease | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:1227 | neutropenia | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:3082 | interstitial lung disease | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:3770 | pulmonary fibrosis | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:3753 | Hermansky-Pudlak syndrome | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:0060540 | Hermansky-Pudlak syndrome 2 | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:2223 | platelet storage pool deficiency | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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DOID:0081430 | intellectual developmental disorder with autistic features and language delay, with or without seizures | HGNC:29364 | Homo sapiens (human) | 85461 | TANC1 |
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DOID:7693 | abdominal aortic aneurysm | SGD:S000001435 | Saccharomyces cerevisiae S288C | 854634 | VTH1 |
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DOID:10652 | Alzheimer's disease | SGD:S000001435 | Saccharomyces cerevisiae S288C | 854634 | VTH1 |
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DOID:9266 | cystinuria | SGD:S000001434 | Saccharomyces cerevisiae S288C | 854635 | IMA3 |
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DOID:1574 | alcohol use disorder | HGNC:30580 | Homo sapiens (human) | 85464 | SSH2 |
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DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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DOID:9352 | type 2 diabetes mellitus | SGD:S000001417 | Saccharomyces cerevisiae S288C | 854651 | GUT2 |
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DOID:1324 | lung cancer | SGD:S000001411 | Saccharomyces cerevisiae S288C | 854657 | MLP2 |
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DOID:0060308 | autosomal recessive intellectual developmental disorder | SGD:S000001411 | Saccharomyces cerevisiae S288C | 854657 | MLP2 |
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DOID:14330 | Parkinson's disease | SGD:S000001357 | Saccharomyces cerevisiae S288C | 854713 | PRK1 |
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DOID:0070185 | X-linked spermatogenic failure 2 | SGD:S000001335 | Saccharomyces cerevisiae S288C | 854737 | SPO22 |
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DOID:0111474 | combined oxidative phosphorylation deficiency 1 | HGNC:13780 | Homo sapiens (human) | 85476 | GFM1 |
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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