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:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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DOID:1793 | pancreatic cancer | MGI:2136878 | Mus musculus (house mouse) | 93961 | B3galt5 |
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DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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DOID:2841 | asthma | HGNC:16036 | Homo sapiens (human) | 94101 | ORMDL1 |
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DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | MGI:2149820 | Mus musculus (house mouse) | 94181 | Nans |
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DOID:0060050 | autoimmune disease of blood | MGI:2151071 | Mus musculus (house mouse) | 94192 | C1galt1 |
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DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:9743 | diabetic neuropathy | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:8947 | diabetic retinopathy | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:783 | end stage renal disease | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:4977 | lymphedema | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:10763 | hypertension | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:7148 | rheumatoid arthritis | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:6432 | pulmonary hypertension | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:4450 | renal cell carcinoma | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:3407 | carotid artery disease | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:10923 | sickle cell anemia | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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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