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:0110860 | polycystic kidney disease 3 | SGD:S000000433 | Saccharomyces cerevisiae S288C | 852530 | ROT2 |
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DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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DOID:0110858 | polycystic kidney disease 1 | RGD:3130 | Rattus norvegicus (Norway rat) | 24577 | Myc |
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DOID:0110858 | polycystic kidney disease 1 | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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DOID:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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DOID:0110798 | hereditary spastic paraplegia 46 | FB:FBgn0028916 | Drosophila melanogaster (fruit fly) | 34835 | CG33090 |
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DOID:0110798 | hereditary spastic paraplegia 46 | MGI:2654325 | Mus musculus (house mouse) | 230101 | Gba2 |
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DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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DOID:0110777 | hereditary spastic paraplegia 26 | ZFIN:ZDB-GENE-100728-3 | Danio rerio (zebrafish) | 793635 | b4galnt1b |
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DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-17345437 | Xenopus laevis (African clawed frog) | 108709867 | b4galnt1.S |
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DOID:0110777 | hereditary spastic paraplegia 26 | ZFIN:ZDB-GENE-070112-1462 | Danio rerio (zebrafish) | 558684 | b4galnt1a |
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DOID:0110777 | hereditary spastic paraplegia 26 | MGI:1342057 | Mus musculus (house mouse) | 14421 | B4galnt1 |
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DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-960512 | Xenopus tropicalis (tropical clawed frog) | 100145208 | b4galnt1 |
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DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-960515 | Xenopus laevis (African clawed frog) | 379299 | b4galnt1.L |
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DOID:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
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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