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:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
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DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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DOID:0060363 | glycerol kinase deficiency | RGD:70893 | Rattus norvegicus (Norway rat) | 79223 | Gk |
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DOID:0060363 | glycerol kinase deficiency | WB:WBGene00020007 | Caenorhabditis elegans | 173747 | R11F4.1 |
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DOID:0060363 | glycerol kinase deficiency | MGI:1329027 | Mus musculus (house mouse) | 14626 | Gk2 |
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DOID:0060363 | glycerol kinase deficiency | HGNC:4291 | Homo sapiens (human) | 2712 | GK2 |
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DOID:0060363 | glycerol kinase deficiency | SGD:S000001024 | Saccharomyces cerevisiae S288C | 856353 | GUT1 |
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DOID:0060363 | glycerol kinase deficiency | MGI:106594 | Mus musculus (house mouse) | 14933 | Gk |
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DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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DOID:0060462 | Desbuquois dysplasia | Xenbase:XB-GENE-17343461 | Xenopus laevis (African clawed frog) | 108703114 | xylt1.S |
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DOID:0060462 | Desbuquois dysplasia | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:0060462 | Desbuquois dysplasia | Xenbase:XB-GENE-949399 | Xenopus tropicalis (tropical clawed frog) | 100145490 | xylt1 |
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DOID:0060462 | Desbuquois dysplasia | Xenbase:XB-GENE-949402 | Xenopus laevis (African clawed frog) | 444363 | xylt1.L |
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DOID:0060462 | Desbuquois dysplasia | FB:FBgn0015360 | Drosophila melanogaster (fruit fly) | 38288 | oxt | CG32300 |
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DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:0060462 | Desbuquois dysplasia | ZFIN:ZDB-GENE-111017-2 | Danio rerio (zebrafish) | 560951 | xylt1 |
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DOID:0060462 | Desbuquois dysplasia | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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DOID:0060462 | Desbuquois dysplasia | RGD:620093 | Rattus norvegicus (Norway rat) | 64133 | Xylt1 |
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DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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DOID:0060470 | salt and pepper syndrome | RGD:620875 | Rattus norvegicus (Norway rat) | 83505 | St3gal5 |
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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