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:0110645 | long QT syndrome 2 | FB:FBgn0052076 | Drosophila melanogaster (fruit fly) | 326193 | Alg10 | CG32076 |
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DOID:0110645 | long QT syndrome 2 | Xenbase:XB-GENE-976267 | Xenopus tropicalis (tropical clawed frog) | 548946 | alg10 |
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DOID:0110645 | long QT syndrome 2 | ZFIN:ZDB-GENE-110310-8 | Danio rerio (zebrafish) | 100331575 | alg10 |
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DOID:0110645 | long QT syndrome 2 | SGD:S000003459 | Saccharomyces cerevisiae S288C | 853142 | DIE2 |
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DOID:0110645 | long QT syndrome 2 | RGD:708500 | Rattus norvegicus (Norway rat) | 245960 | Alg10 |
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DOID:0110644 | long QT syndrome 1 | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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DOID:0110644 | long QT syndrome 1 | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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DOID:0110644 | long QT syndrome 1 | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | Xenbase:XB-GENE-6250446 | Xenopus tropicalis (tropical clawed frog) | 100498555 | large1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | Xenbase:XB-GENE-17340884 | Xenopus laevis (African clawed frog) | 108712551 | large1.S |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | ZFIN:ZDB-GENE-061204-1 | Danio rerio (zebrafish) | 446213 | large1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | Xenbase:XB-GENE-17343600 | Xenopus laevis (African clawed frog) | 108704366 | large1.L |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | MGI:1342270 | Mus musculus (house mouse) | 16795 | Large1 |
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DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | RGD:1308895 | Rattus norvegicus (Norway rat) | 361368 | Large1 |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | Xenbase:XB-GENE-17338998 | Xenopus laevis (African clawed frog) | 108698503 | fkrp.L |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | RGD:1305852 | Rattus norvegicus (Norway rat) | 308390 | Fkrp |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | Xenbase:XB-GENE-964270 | Xenopus tropicalis (tropical clawed frog) | 100145309 | fkrp |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | FB:FBgn0034567 | Drosophila melanogaster (fruit fly) | 37375 | CG15651 | CG15651 |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | ZFIN:ZDB-GENE-070412-4 | Danio rerio (zebrafish) | 571426 | fkrp |
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DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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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