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:9970 | obesity | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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DOID:0050873 | follicular lymphoma | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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DOID:6432 | pulmonary hypertension | HGNC:4820 | Homo sapiens (human) | 3038 | HAS3 |
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DOID:557 | kidney disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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DOID:5844 | myocardial infarction | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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DOID:1793 | pancreatic cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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DOID:4852 | pleomorphic xanthoastrocytoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:2986 | IgA glomerulonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:3770 | pulmonary fibrosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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DOID:11396 | pulmonary edema | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:114 | heart disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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DOID:162 | cancer | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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DOID:9268 | glycine encephalopathy | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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DOID:4450 | renal cell carcinoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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DOID:11335 | sarcoidosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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DOID:2957 | pulmonary tuberculosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:783 | end stage renal disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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DOID:2367 | neuroaxonal dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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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