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:3211 | lysosomal storage disease | HGNC:11753 | Homo sapiens (human) | 7942 | TFEB |
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DOID:10763 | hypertension | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:0110144 | Bartter disease type 3 | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:0050450 | Gitelman syndrome | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:445 | Bartter disease | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:0110146 | Bartter disease type 4b | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:423 | myopathy | RGD:628639 | Rattus norvegicus (Norway rat) | 79430 | Clcnkb |
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DOID:0060870 | isolated growth hormone deficiency | RGD:68429 | Rattus norvegicus (Norway rat) | 79438 | Igfals |
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DOID:1184 | nephrotic syndrome | RGD:68429 | Rattus norvegicus (Norway rat) | 79438 | Igfals |
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DOID:3490 | Noonan syndrome | RGD:68429 | Rattus norvegicus (Norway rat) | 79438 | Igfals |
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DOID:0080552 | congenital disorder of glycosylation Ia | RGD:68429 | Rattus norvegicus (Norway rat) | 79438 | Igfals |
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DOID:8689 | anorexia nervosa | RGD:68429 | Rattus norvegicus (Norway rat) | 79438 | Igfals |
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DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:28707 | Homo sapiens (human) | 79447 | PAGR1 |
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DOID:3748 | esophagus squamous cell carcinoma | HGNC:28707 | Homo sapiens (human) | 79447 | PAGR1 |
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DOID:3635 | congenital myasthenic syndrome | RGD:69277 | Rattus norvegicus (Norway rat) | 79557 | Chrna1 |
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DOID:0110663 | congenital myasthenic syndrome 1A | RGD:69277 | Rattus norvegicus (Norway rat) | 79557 | Chrna1 |
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DOID:0110662 | congenital myasthenic syndrome 1B | RGD:69277 | Rattus norvegicus (Norway rat) | 79557 | Chrna1 |
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DOID:13374 | fibrodysplasia ossificans progressiva | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:1405 | primary angle-closure glaucoma | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:13641 | exfoliation syndrome | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:13129 | severe pre-eclampsia | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:1070 | primary open angle glaucoma | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:1793 | pancreatic cancer | RGD:620200 | Rattus norvegicus (Norway rat) | 79558 | Acvr1 |
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DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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DOID:3534 | Lafora disease | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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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