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:11832 | visual epilepsy | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:3454 | brain infarction | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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DOID:10652 | Alzheimer's disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:9352 | type 2 diabetes mellitus | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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DOID:0110914 | infantile hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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DOID:0060060 | non-Hodgkin lymphoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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DOID:5844 | myocardial infarction | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:1307 | dementia | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:74 | hematopoietic system disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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DOID:7941 | Barrett's adenocarcinoma | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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DOID:1749 | squamous cell carcinoma | HGNC:6710 | Homo sapiens (human) | 4048 | LTA4H |
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DOID:1184 | nephrotic syndrome | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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DOID:0060903 | thrombosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:2297 | leptospirosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:14330 | Parkinson's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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DOID:1793 | pancreatic cancer | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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DOID:0080433 | developmental and epileptic encephalopathy 51 | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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DOID:5844 | myocardial infarction | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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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