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:7693 | abdominal aortic aneurysm | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:5844 | myocardial infarction | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:9970 | obesity | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:9538 | multiple myeloma | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:10825 | essential hypertension | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:13963 | nuclear senile cataract | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:224 | transient cerebral ischemia | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:9352 | type 2 diabetes mellitus | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:9743 | diabetic neuropathy | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:6000 | congestive heart failure | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:9477 | pulmonary embolism | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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DOID:0112136 | severe congenital neutropenia 4 | ZFIN:ZDB-GENE-061215-19 | Danio rerio (zebrafish) | 790919 | g6pc3 |
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DOID:9212 | pityriasis rubra pilaris | HGNC:16446 | Homo sapiens (human) | 79092 | CARD14 |
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DOID:0080475 | psoriasis 2 | HGNC:16446 | Homo sapiens (human) | 79092 | CARD14 |
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DOID:0080118 | mitochondrial complex III deficiency nuclear type 9 | HGNC:34399 | Homo sapiens (human) | 790955 | UQCC3 |
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DOID:1459 | hypothyroidism | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:0050328 | congenital hypothyroidism | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:1498 | cholera | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:0050338 | primary bacterial infectious disease | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:0112189 | thyroid dyshormonogenesis 6 | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:8778 | Crohn's disease | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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DOID:8577 | ulcerative colitis | RGD:628761 | Rattus norvegicus (Norway rat) | 79107 | Duox2 |
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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