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:0112195 | spondyloperipheral dysplasia | Xenbase:XB-GENE-6252613 | Xenopus laevis (African clawed frog) | 397738 | col2a1.L |
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DOID:4948 | gallbladder carcinoma | Xenbase:XB-GENE-6488967 | Xenopus laevis (African clawed frog) | 108698211 | abo.2.L |
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DOID:1485 | cystic fibrosis | Xenbase:XB-GENE-865765 | Xenopus laevis (African clawed frog) | 397778 | tgfb1.L |
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DOID:2841 | asthma | Xenbase:XB-GENE-6488967 | Xenopus laevis (African clawed frog) | 108698211 | abo.2.L |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-920741 | Xenopus laevis (African clawed frog) | 398006 | insr.L |
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DOID:3049 | Churg-Strauss syndrome | Xenbase:XB-GENE-6487060 | Xenopus laevis (African clawed frog) | 108696016 | gfra1.L |
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DOID:0060041 | autism spectrum disorder | Xenbase:XB-GENE-960094 | Xenopus laevis (African clawed frog) | 397839 | itga4.S |
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DOID:0050731 | vitamin B12 deficiency | Xenbase:XB-GENE-17341135 | Xenopus laevis (African clawed frog) | 108696739 | fut2.L |
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DOID:9352 | type 2 diabetes mellitus | Xenbase:XB-GENE-962202 | Xenopus laevis (African clawed frog) | 373759 | cnr1.S |
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DOID:10763 | hypertension | Xenbase:XB-GENE-17344447 | Xenopus laevis (African clawed frog) | 108707435 | ace2.L |
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DOID:3892 | insulinoma | Xenbase:XB-GENE-865765 | Xenopus laevis (African clawed frog) | 397778 | tgfb1.L |
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DOID:0080333 | aortic valve disease 1 | Xenbase:XB-GENE-865261 | Xenopus laevis (African clawed frog) | 394367 | notch1.S |
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DOID:0060318 | acute promyelocytic leukemia | Xenbase:XB-GENE-923178 | Xenopus laevis (African clawed frog) | 397762 | ncam1.L |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | Xenbase:XB-GENE-1010249 | Xenopus laevis (African clawed frog) | 398597 | b3gat3.L |
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DOID:8725 | vascular dementia | Xenbase:XB-GENE-491658 | Xenopus laevis (African clawed frog) | 380341 | pon2.L |
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DOID:10584 | retinitis pigmentosa | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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DOID:12554 | hemolytic-uremic syndrome | Xenbase:XB-GENE-941235 | Xenopus laevis (African clawed frog) | 495031 | c1galt1c1.L |
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DOID:0050920 | tonsil squamous cell carcinoma | Xenbase:XB-GENE-17330101 | Xenopus laevis (African clawed frog) | 399347 | fgfr3.S |
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DOID:0112281 | spondyloepiphyseal dysplasia Stanescu type | Xenbase:XB-GENE-6252613 | Xenopus laevis (African clawed frog) | 397738 | col2a1.L |
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DOID:0110658 | congenital myasthenic syndrome 15 | Xenbase:XB-GENE-17331641 | Xenopus laevis (African clawed frog) | 108715652 | alg14.S |
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DOID:4450 | renal cell carcinoma | Xenbase:XB-GENE-865617 | Xenopus laevis (African clawed frog) | 399375 | wif1.S |
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DOID:0060224 | atrial fibrillation | Xenbase:XB-GENE-865765 | Xenopus laevis (African clawed frog) | 397778 | tgfb1.L |
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DOID:14766 | renal agenesis | Xenbase:XB-GENE-17343984 | Xenopus laevis (African clawed frog) | 108697312 | gfra1.S |
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DOID:4948 | gallbladder carcinoma | Xenbase:XB-GENE-5962623 | Xenopus laevis (African clawed frog) | 495825 | abo.3.L |
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DOID:9256 | colorectal cancer | Xenbase:XB-GENE-484957 | Xenopus laevis (African clawed frog) | 399170 | akt1.S |
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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