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:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-953845 | Xenopus tropicalis (tropical clawed frog) | 550071 | hs6st1 |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | RGD:1309218 | Rattus norvegicus (Norway rat) | 316325 | Hs6st1 |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-953851 | Xenopus laevis (African clawed frog) | 373566 | hs6st1.S |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | MGI:1354958 | Mus musculus (house mouse) | 50785 | Hs6st1 |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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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:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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DOID:0090056 | dystonia 12 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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DOID:0090056 | dystonia 12 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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DOID:0090005 | Schwartz-Jampel syndrome 1 | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | RGD:3734 | Rattus norvegicus (Norway rat) | 24788 | Sord |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000004060 | Saccharomyces cerevisiae S288C | 850759 | XYL2 |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | MGI:98266 | Mus musculus (house mouse) | 20322 | Sord |
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DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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DOID:0081385 | ataxia-telangiectasia-like disorder-2 | RGD:3269 | Rattus norvegicus (Norway rat) | 25737 | Pcna |
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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