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:1338 | congenital dyserythropoietic anemia | FB:FBgn0011740 | Drosophila melanogaster (fruit fly) | 41126 | α-Man-IIa | CG18802 |
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DOID:1338 | congenital dyserythropoietic anemia | RGD:3038 | Rattus norvegicus (Norway rat) | 25478 | Man2a1 |
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DOID:1338 | congenital dyserythropoietic anemia | MGI:104669 | Mus musculus (house mouse) | 17158 | Man2a1 |
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DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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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: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:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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DOID:0070262 | congenital disorder of glycosylation type IIj | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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DOID:0070261 | congenital disorder of glycosylation type IIi | SGD:S000004996 | Saccharomyces cerevisiae S288C | 855676 | COG5 |
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DOID:0070260 | congenital disorder of glycosylation type IIh | SGD:S000004536 | Saccharomyces cerevisiae S288C | 854904 | COG8 |
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DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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DOID:0070256 | congenital disorder of glycosylation type IId | ZFIN:ZDB-GENE-061013-84 | Danio rerio (zebrafish) | 768123 | b4galt1l |
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DOID:0070256 | congenital disorder of glycosylation type IId | Xenbase:XB-GENE-17340428 | Xenopus laevis (African clawed frog) | 108706813 | b4galt1.2.S |
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DOID:0070256 | congenital disorder of glycosylation type IId | FB:FBgn0027538 | Drosophila melanogaster (fruit fly) | 36585 | β4GalNAcTA | CG8536 |
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DOID:0070256 | congenital disorder of glycosylation type IId | WB:WBGene00000269 | Caenorhabditis elegans | 190668 | bre-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 v4.0.0
Last updated: August 19, 2024