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:9351 | diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0111100 | maturity-onset diabetes of the young type 2 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:10763 | hypertension | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:2018 | hyperinsulinism | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:3393 | coronary artery disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:9452 | steatotic liver disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:4195 | hyperglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0050524 | maturity-onset diabetes of the young | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:4194 | glucose metabolism disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:9970 | obesity | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:9993 | hypoglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:557 | kidney disease | HGNC:4201 | Homo sapiens (human) | 2648 | KAT2A |
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DOID:3908 | lung non-small cell carcinoma | HGNC:4201 | Homo sapiens (human) | 2648 | KAT2A |
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DOID:114 | heart disease | HGNC:4201 | Homo sapiens (human) | 2648 | KAT2A |
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DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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DOID:9268 | glycine encephalopathy | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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DOID:9252 | amino acid metabolic disorder | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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DOID:1168 | familial hyperlipidemia | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:9970 | obesity | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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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