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:8466 | retinal degeneration | HGNC:11761 | Homo sapiens (human) | 7980 | TFPI2 |
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DOID:9119 | acute myeloid leukemia | HGNC:11761 | Homo sapiens (human) | 7980 | TFPI2 |
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DOID:11247 | disseminated intravascular coagulation | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:1240 | leukemia | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:0081267 | graft-versus-host disease | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:224 | transient cerebral ischemia | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:10159 | osteonecrosis | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:2216 | factor V deficiency | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:0060224 | atrial fibrillation | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:5844 | myocardial infarction | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:0111144 | preterm premature rupture of the membranes | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:14115 | toxic shock syndrome | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:3770 | pulmonary fibrosis | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:12134 | factor VIII deficiency | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:5425 | ovarian hyperstimulation syndrome | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:14566 | disease of cellular proliferation | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:1184 | nephrotic syndrome | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:2451 | protein S deficiency | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:9074 | systemic lupus erythematosus | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:1168 | familial hyperlipidemia | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:10591 | pre-eclampsia | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:9351 | diabetes mellitus | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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DOID:10772 | thrombotic thrombocytopenic purpura | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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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