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:1287 | cardiovascular system disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:10652 | Alzheimer's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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DOID:0050560 | Walker-Warburg syndrome | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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DOID:3969 | thyroid gland papillary carcinoma | HGNC:12755 | Homo sapiens (human) | 10885 | WDR3 |
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DOID:1574 | alcohol use disorder | MGI:1918614 | Mus musculus (house mouse) | 108829 | Jmjd1c |
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DOID:2945 | severe acute respiratory syndrome | HGNC:1820 | Homo sapiens (human) | 1088 | CEACAM8 |
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DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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DOID:0110014 | age related macular degeneration 1 | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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DOID:0040094 | autoimmune glomerulonephritis | HGNC:3696 | Homo sapiens (human) | 10875 | FGL2 |
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DOID:9970 | obesity | HGNC:7859 | Homo sapiens (human) | 10874 | NMU |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-17339244 | Xenopus laevis (African clawed frog) | 108719811 | plcd1.S |
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DOID:0080081 | nonsyndromic congenital nail disorder 3 | Xenbase:XB-GENE-17339244 | Xenopus laevis (African clawed frog) | 108719811 | plcd1.S |
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DOID:9256 | colorectal cancer | Xenbase:XB-GENE-17330127 | Xenopus laevis (African clawed frog) | 108719043 | galnt12.L |
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DOID:0080573 | congenital disorder of glycosylation Ix | Xenbase:XB-GENE-17341012 | Xenopus laevis (African clawed frog) | 108718938 | stt3b.L |
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DOID:0080081 | nonsyndromic congenital nail disorder 3 | Xenbase:XB-GENE-6485790 | Xenopus laevis (African clawed frog) | 108718712 | plcd1.L |
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DOID:10652 | Alzheimer's disease | Xenbase:XB-GENE-6485790 | Xenopus laevis (African clawed frog) | 108718712 | plcd1.L |
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DOID:1574 | alcohol use disorder | Xenbase:XB-GENE-17330217 | Xenopus laevis (African clawed frog) | 108718183 | st6gal1.S |
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DOID:1094 | attention deficit hyperactivity disorder | Xenbase:XB-GENE-6486769 | Xenopus laevis (African clawed frog) | 108717884 | ust.S |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | Xenbase:XB-GENE-17344746 | Xenopus laevis (African clawed frog) | 108717671 | ppp1cb.S |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-17335472 | Xenopus laevis (African clawed frog) | 108717161 | hs6st1.L |
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DOID:1574 | alcohol use disorder | Xenbase:XB-GENE-6486698 | Xenopus laevis (African clawed frog) | 108717116 | st6gal1.L |
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DOID:5419 | schizophrenia | Xenbase:XB-GENE-17334879 | Xenopus laevis (African clawed frog) | 108716933 | b3gat2.L |
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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