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 | October 9, 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:0070343 | CSF1R-related brain malformation and osteopetrosis | MGI:1339758 | Mus musculus (house mouse) | 12978 | Csf1r |
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DOID:0070343 | CSF1R-related brain malformation and osteopetrosis | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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DOID:0070343 | CSF1R-related brain malformation and osteopetrosis | ZFIN:ZDB-GENE-001205-1 | Danio rerio (zebrafish) | 64274 | csf1ra |
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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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DOID:0070342 | adult-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | Aralar |
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DOID:0070342 | adult-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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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 | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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DOID:0070341 | neonatal-onset type II citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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DOID:0070341 | neonatal-onset type II citrullinemia | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | Aralar |
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DOID:0070340 | classic citrullinemia | HGNC:758 | Homo sapiens (human) | 445 | ASS1 |
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DOID:0070340 | classic citrullinemia | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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DOID:0070339 | cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | HGNC:15822 | Homo sapiens (human) | 55074 | OXR1 |
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DOID:0070339 | cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | RGD:621857 | Rattus norvegicus (Norway rat) | 117520 | Oxr1 |
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DOID:0070339 | cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | MGI:2179326 | Mus musculus (house mouse) | 170719 | Oxr1 |
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DOID:0070338 | cerebellar hypoplasia | HGNC:15998 | Homo sapiens (human) | 89795 | NAV3 |
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DOID:0070338 | cerebellar hypoplasia | HGNC:15997 | Homo sapiens (human) | 89797 | NAV2 |
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DOID:0070338 | cerebellar hypoplasia | HGNC:15989 | Homo sapiens (human) | 89796 | NAV1 |
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DOID:0070338 | cerebellar hypoplasia | MGI:2183683 | Mus musculus (house mouse) | 215690 | Nav1 |
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DOID:0070337 | epithelial recurrent erosion dystrophy | MGI:88450 | Mus musculus (house mouse) | 12821 | Col17a1 |
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DOID:0070337 | epithelial recurrent erosion dystrophy | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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DOID:0070336 | arthrogryposis multiplex congenita-6 | HGNC:7720 | Homo sapiens (human) | 4703 | NEB |
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DOID:0070336 | arthrogryposis multiplex congenita-6 | MGI:97292 | Mus musculus (house mouse) | 17996 | Neb |
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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 v4.1.0
Last updated: December 9, 2024