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:9952 | acute lymphoblastic leukemia | Xenbase:XB-GENE-969944 | Xenopus tropicalis (tropical clawed frog) | 549858 | abo.2 |
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DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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DOID:9352 | type 2 diabetes mellitus | MGI:1097693 | Mus musculus (house mouse) | 18294 | Ogg1 |
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DOID:5082 | liver cirrhosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:0050579 | glycogen storage disease XV | RGD:621785 | Rattus norvegicus (Norway rat) | 81675 | Gyg1 |
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DOID:14504 | Niemann-Pick disease | WB:WBGene00000212 | Caenorhabditis elegans | 181323 | asm-2 |
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DOID:9970 | obesity | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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DOID:1926 | Gaucher's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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DOID:9538 | multiple myeloma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:9351 | diabetes mellitus | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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DOID:8893 | psoriasis | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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DOID:11088 | asphyxia neonatorum | HGNC:4606 | Homo sapiens (human) | 2923 | PDIA3 |
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DOID:12377 | spinal muscular atrophy | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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DOID:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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DOID:14330 | Parkinson's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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DOID:12930 | dilated cardiomyopathy | RGD:1305852 | Rattus norvegicus (Norway rat) | 308390 | Fkrp |
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DOID:12361 | Graves' disease | RGD:621168 | Rattus norvegicus (Norway rat) | 81528 | Ogg1 |
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DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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DOID:684 | hepatocellular carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:5409 | lung small cell carcinoma | MGI:97583 | Mus musculus (house mouse) | 18708 | Pik3r1 |
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DOID:0080365 | endometrial hyperplasia | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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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