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:11714 | gestational diabetes | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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DOID:0014667 | disease of metabolism | Xenbase:XB-GENE-6252363 | Xenopus laevis (African clawed frog) | 378696 | ins.S |
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DOID:3525 | middle cerebral artery infarction | MGI:1919959 | Mus musculus (house mouse) | 72709 | C1qtnf6 |
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DOID:0080027 | spondyloepimetaphyseal dysplasia | Xenbase:XB-GENE-6258353 | Xenopus tropicalis (tropical clawed frog) | 394828 | col2a1 |
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DOID:1405 | primary angle-closure glaucoma | Xenbase:XB-GENE-1020972 | Xenopus laevis (African clawed frog) | 447583 | myrf.L |
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DOID:0050753 | cerebellar ataxia | MGI:2384560 | Mus musculus (house mouse) | 234734 | Aars1 |
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DOID:635 | acquired immunodeficiency syndrome | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:0111128 | focal segmental glomerulosclerosis 1 | FB:FBgn0016122 | Drosophila melanogaster (fruit fly) | 34189 | Acer |
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DOID:0111668 | Kohlschutter-Tonz syndrome | MGI:3037150 | Mus musculus (house mouse) | 237831 | Slc13a5 |
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DOID:3021 | acute kidney failure | HGNC:9452 | Homo sapiens (human) | 10544 | PROCR |
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DOID:11121 | pulpitis | MGI:107656 | Mus musculus (house mouse) | 15978 | Ifng |
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DOID:0050989 | episodic ataxia type 1 | HGNC:6226 | Homo sapiens (human) | 3743 | KCNA7 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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DOID:3490 | Noonan syndrome | HGNC:9051 | Homo sapiens (human) | 5327 | PLAT |
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DOID:1059 | intellectual disability | SGD:S000002815 | Saccharomyces cerevisiae S288C | 852016 | TRS120 |
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DOID:0050766 | choreaacanthocytosis | HGNC:1908 | Homo sapiens (human) | 23230 | VPS13A |
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DOID:9408 | acute myocardial infarction | HGNC:6149 | Homo sapiens (human) | 3684 | ITGAM |
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DOID:3525 | middle cerebral artery infarction | RGD:2559 | Rattus norvegicus (Norway rat) | 24335 | Epo |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | Xenbase:XB-GENE-1006906 | Xenopus tropicalis (tropical clawed frog) | 100490100 | pomt2 |
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DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | WB:WBGene00005642 | Caenorhabditis elegans | 178585 | srp-1 |
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DOID:3070 | high grade glioma | HGNC:2730 | Homo sapiens (human) | 780 | DDR1 |
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DOID:6000 | congestive heart failure | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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DOID:0110870 | congenital stationary night blindness 1A | MGI:2448607 | Mus musculus (house mouse) | 236690 | Nyx |
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DOID:9352 | type 2 diabetes mellitus | RGD:3433 | Rattus norvegicus (Norway rat) | 25526 | Ptgds |
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DOID:3068 | glioblastoma | MGI:1928894 | Mus musculus (house mouse) | 57808 | Rpl35a |
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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