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:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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DOID:0070264 | congenital disorder of glycosylation type IIl | SGD:S000004986 | Saccharomyces cerevisiae S288C | 855687 | COG6 |
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DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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DOID:0070265 | congenital disorder of glycosylation type IIm | FB:FBgn0024994 | Drosophila melanogaster (fruit fly) | 31255 | Ugalt | CG2675 |
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DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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DOID:0070295 | primary autosomal dominant microcephaly 18 | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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DOID:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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DOID:0070303 | multiple epiphyseal dysplasia 1 | FB:FBgn0031850 | Drosophila melanogaster (fruit fly) | 33941 | Tsp | CG11326 |
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DOID:0070311 | oligoasthenoteratozoospermia | HGNC:26125 | Homo sapiens (human) | 64847 | SPATA20 |
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DOID:0070311 | oligoasthenoteratozoospermia | MGI:2183449 | Mus musculus (house mouse) | 217116 | Spata20 |
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DOID:0070311 | oligoasthenoteratozoospermia | RGD:735087 | Rattus norvegicus (Norway rat) | 360604 | Spata20 |
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DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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DOID:0070329 | mitochondrial DNA depletion syndrome | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0070329 | mitochondrial DNA depletion syndrome | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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DOID:0070341 | neonatal-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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DOID:0070341 | neonatal-onset type II citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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DOID:0070342 | adult-onset type II citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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DOID:0070342 | adult-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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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