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:9261 | nasopharynx carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:0081292 | traumatic brain injury | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:2152 | ovary epithelial cancer | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:10534 | stomach cancer | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:3910 | lung adenocarcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:3069 | malignant astrocytoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:0050865 | tongue squamous cell carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:5082 | liver cirrhosis | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:0080199 | colorectal carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:1612 | breast cancer | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:3907 | lung squamous cell carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:684 | hepatocellular carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:11446 | sciatic neuropathy | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:3748 | esophagus squamous cell carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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DOID:0050718 | vitamin metabolic disorder | HGNC:11041 | Homo sapiens (human) | 8884 | SLC5A6 |
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DOID:0070371 | leukoencephalopathy with vanishing white matter 4 | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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DOID:0060868 | leukoencephalopathy with vanishing white matter | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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DOID:10579 | leukodystrophy | HGNC:3266 | Homo sapiens (human) | 8894 | EIF2S2 |
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DOID:0111225 | centronuclear myopathy X-linked | HGNC:7451 | Homo sapiens (human) | 8897 | MTMR3 |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7451 | Homo sapiens (human) | 8897 | MTMR3 |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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DOID:0111225 | centronuclear myopathy X-linked | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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DOID:423 | myopathy | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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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