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:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | FB:FBgn0038045 | Drosophila melanogaster (fruit fly) | 41528 | NANS |
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DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | MGI:2149820 | Mus musculus (house mouse) | 94181 | Nans |
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DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | WB:WBGene00005026 | Caenorhabditis elegans | 174517 | sqv-8 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | HGNC:923 | Homo sapiens (human) | 26229 | B3GAT3 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | MGI:1919977 | Mus musculus (house mouse) | 72727 | B3gat3 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | RGD:1311968 | Rattus norvegicus (Norway rat) | 293722 | B3gat3 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | FB:FBgn0066114 | Drosophila melanogaster (fruit fly) | 251900 | GlcAT-I | CG32775 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | Xenbase:XB-GENE-1010243 | Xenopus tropicalis (tropical clawed frog) | 594895 | b3gat3 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | ZFIN:ZDB-GENE-020419-3 | Danio rerio (zebrafish) | 192334 | b3gat3 |
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DOID:0080575 | Larsen-like syndrome B3GAT3 type | Xenbase:XB-GENE-1010249 | Xenopus laevis (African clawed frog) | 398597 | b3gat3.L |
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DOID:0080573 | congenital disorder of glycosylation Ix | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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DOID:0080573 | congenital disorder of glycosylation Ix | RGD:1311563 | Rattus norvegicus (Norway rat) | 363160 | Stt3b |
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DOID:0080573 | congenital disorder of glycosylation Ix | Xenbase:XB-GENE-969897 | Xenopus laevis (African clawed frog) | 100380973 | stt3b.S |
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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:0080573 | congenital disorder of glycosylation Ix | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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DOID:0080573 | congenital disorder of glycosylation Ix | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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DOID:0080573 | congenital disorder of glycosylation Ix | ZFIN:ZDB-GENE-030131-2638 | Danio rerio (zebrafish) | 323918 | stt3b |
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DOID:0080573 | congenital disorder of glycosylation Ix | FB:FBgn0011336 | Drosophila melanogaster (fruit fly) | 43005 | Stt3B | CG7748 |
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DOID:0080573 | congenital disorder of glycosylation Ix | SGD:S000002990 | Saccharomyces cerevisiae S288C | 852862 | STT3 |
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DOID:0080572 | congenital disorder of glycosylation Iw | FB:FBgn0011336 | Drosophila melanogaster (fruit fly) | 43005 | Stt3B | CG7748 |
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DOID:0080572 | congenital disorder of glycosylation Iw | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:6172 | Homo sapiens (human) | 3703 | STT3A |
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DOID:0080572 | congenital disorder of glycosylation Iw | RGD:1565793 | Rattus norvegicus (Norway rat) | 500972 | Stt3a |
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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