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:0110429 | dilated cardiomyopathy 1H | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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DOID:0110429 | dilated cardiomyopathy 1H | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0110429 | dilated cardiomyopathy 1H | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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DOID:0110429 | dilated cardiomyopathy 1H | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0110429 | dilated cardiomyopathy 1H | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0110409 | retinitis pigmentosa 46 | SGD:S000004982 | Saccharomyces cerevisiae S288C | 855691 | IDH1 |
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DOID:0110409 | retinitis pigmentosa 46 | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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DOID:0110389 | retinitis pigmentosa 73 | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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DOID:0110370 | retinitis pigmentosa 55 | MGI:1927136 | Mus musculus (house mouse) | 56297 | Arl6 |
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DOID:0110366 | retinitis pigmentosa 33 | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110312 | hypertrophic cardiomyopathy 6 | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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DOID:0110312 | hypertrophic cardiomyopathy 6 | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | Xenbase:XB-GENE-17338998 | Xenopus laevis (African clawed frog) | 108698503 | fkrp.L |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | ZFIN:ZDB-GENE-070412-4 | Danio rerio (zebrafish) | 571426 | fkrp |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | RGD:1305852 | Rattus norvegicus (Norway rat) | 308390 | Fkrp |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | Xenbase:XB-GENE-964270 | Xenopus tropicalis (tropical clawed frog) | 100145309 | fkrp |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | FB:FBgn0034567 | Drosophila melanogaster (fruit fly) | 37375 | CG15651 | CG15651 |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | SGD:S000005848 | Saccharomyces cerevisiae S288C | 854499 | PMT3 |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | Xenbase:XB-GENE-6489079 | Xenopus laevis (African clawed frog) | 108698684 | pomt2.L |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | FB:FBgn0086368 | Drosophila melanogaster (fruit fly) | 31024 | tw | CG12311 |
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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