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:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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DOID:0060728 | NGLY1-deficiency | HGNC:17646 | Homo sapiens (human) | 55768 | NGLY1 |
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DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | SGD:S000004483 | Saccharomyces cerevisiae S288C | 854987 | UNG1 |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | MGI:109352 | Mus musculus (house mouse) | 22256 | Ung |
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DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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DOID:0060770 | dextro-looped transposition of the great arteries | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:0060786 | hypomyelinating leukodystrophy | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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DOID:0060806 | syndromic X-linked intellectual disability Hedera type | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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DOID:0060849 | osteoporosis-pseudoglioma syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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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