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:8553 | pyoderma gangrenosum | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:2841 | asthma | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:11476 | osteoporosis | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:1686 | glaucoma | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:6432 | pulmonary hypertension | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:13382 | megaloblastic anemia | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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DOID:557 | kidney disease | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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DOID:0050700 | cardiomyopathy | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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DOID:10273 | heart conduction disease | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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DOID:1826 | epilepsy | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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DOID:1591 | renovascular hypertension | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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DOID:5844 | myocardial infarction | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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DOID:104 | bacterial infectious disease | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:2043 | hepatitis B | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:0080594 | hyper IgE recurrent infection syndrome 2 | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:934 | viral infectious disease | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:3310 | atopic dermatitis | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:0090110 | immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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DOID:809 | cocaine abuse | RGD:69281 | Rattus norvegicus (Norway rat) | 81721 | Chrna6 |
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DOID:1574 | alcohol use disorder | RGD:69281 | Rattus norvegicus (Norway rat) | 81721 | Chrna6 |
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DOID:3635 | congenital myasthenic syndrome | RGD:69281 | Rattus norvegicus (Norway rat) | 81721 | Chrna6 |
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DOID:0050742 | nicotine dependence | RGD:69281 | Rattus norvegicus (Norway rat) | 81721 | Chrna6 |
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DOID:0110670 | congenital myasthenic syndrome 9 | RGD:3211 | Rattus norvegicus (Norway rat) | 81725 | Musk |
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DOID:0111377 | fetal akinesia deformation sequence syndrome 1 | RGD:3211 | Rattus norvegicus (Norway rat) | 81725 | Musk |
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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