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:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | Xenbase:XB-GENE-6488390 | Xenopus laevis (African clawed frog) | 108696563 | b3galt6.L |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | ZFIN:ZDB-GENE-101104-13 | Danio rerio (zebrafish) | 572324 | b3galt6 |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | Xenbase:XB-GENE-17345196 | Xenopus laevis (African clawed frog) | 108697636 | b3galt6.S |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | FB:FBgn0033315 | Drosophila melanogaster (fruit fly) | 35848 | beta3GalTII | CG8734 |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | MGI:2152819 | Mus musculus (house mouse) | 117592 | B3galt6 |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | RGD:1309558 | Rattus norvegicus (Norway rat) | 298690 | B3galt6 |
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DOID:0050800 | cerebral creatine deficiency syndrome 1 | RGD:619711 | Rattus norvegicus (Norway rat) | 50690 | Slc6a8 |
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DOID:0050800 | cerebral creatine deficiency syndrome 1 | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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DOID:0050800 | cerebral creatine deficiency syndrome 1 | MGI:2147834 | Mus musculus (house mouse) | 102857 | Slc6a8 |
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DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | Acox1 |
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DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | SGD:S000003173 | Saccharomyces cerevisiae S288C | 852667 | POX1 |
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DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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DOID:0050795 | cone dystrophy | HGNC:16262 | Homo sapiens (human) | 10413 | YAP1 |
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DOID:0050795 | cone dystrophy | MGI:103262 | Mus musculus (house mouse) | 22601 | Yap1 |
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DOID:0050794 | multiple synostoses syndrome | RGD:2610 | Rattus norvegicus (Norway rat) | 25444 | Fgf9 |
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DOID:0050794 | multiple synostoses syndrome | HGNC:3687 | Homo sapiens (human) | 2254 | FGF9 |
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DOID:0050794 | multiple synostoses syndrome | MGI:104723 | Mus musculus (house mouse) | 14180 | Fgf9 |
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DOID:0050794 | multiple synostoses syndrome | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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DOID:0050794 | multiple synostoses syndrome | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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DOID:0050793 | short QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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DOID:0050793 | short QT syndrome | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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DOID:0050793 | short QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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DOID:0050793 | short QT syndrome | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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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