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:684 | hepatocellular carcinoma | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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DOID:684 | hepatocellular carcinoma | FB:FBgn0015615 | Drosophila melanogaster (fruit fly) | 32627 | SMC3 |
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DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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DOID:10763 | hypertension | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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DOID:0080899 | lung pleomorphic carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:2671 | transitional cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:0050865 | tongue squamous cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:0080202 | adenoid cystic carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:5517 | stomach carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:3910 | lung adenocarcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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DOID:9266 | cystinuria | HGNC:11025 | Homo sapiens (human) | 6519 | SLC3A1 |
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DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0060250 | idiopathic scoliosis | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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DOID:2749 | glycogen storage disease Ia | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0050775 | schneckenbecken dysplasia | HGNC:20800 | Homo sapiens (human) | 23169 | SLC35D1 |
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DOID:0050571 | congenital disorder of glycosylation type II | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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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