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:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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DOID:0111843 | Paganini-Miozzo syndrome | Xenbase:XB-GENE-6039291 | Xenopus tropicalis (tropical clawed frog) | 100496603 | hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | FB:FBgn0038755 | Drosophila melanogaster (fruit fly) | 42380 | Hs6st | CG4451 |
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DOID:0111843 | Paganini-Miozzo syndrome | RGD:1564397 | Rattus norvegicus (Norway rat) | 302489 | Hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | MGI:1354959 | Mus musculus (house mouse) | 50786 | Hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | ZFIN:ZDB-GENE-030909-14 | Danio rerio (zebrafish) | 378450 | hs6st2 |
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DOID:0111842 | Keipert syndrome | FB:FBgn0041604 | Drosophila melanogaster (fruit fly) | 39596 | dlp | CG32146 |
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DOID:0111839 | congenital disorder of glycosylation Icc | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
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DOID:0111839 | congenital disorder of glycosylation Icc | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostgamma | CG7830 |
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DOID:0111839 | congenital disorder of glycosylation Icc | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | OstĪ³ | CG7830 |
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DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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DOID:0111773 | 46,XY sex reversal 8 | SGD:S000002776 | Saccharomyces cerevisiae S288C | 851974 | YPR1 |
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DOID:0111773 | 46,XY sex reversal 8 | SGD:S000005646 | Saccharomyces cerevisiae S288C | 854287 | GCY1 |
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DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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DOID:0111739 | X-linked deafness 1 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:0111681 | glutamate-cysteine ligase deficiency | RGD:619868 | Rattus norvegicus (Norway rat) | 25283 | Gclc |
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DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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DOID:0111681 | glutamate-cysteine ligase deficiency | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:0111680 | essential fructosuria | MGI:1096353 | Mus musculus (house mouse) | 16548 | Khk |
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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