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:674 | cleft palate | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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DOID:11198 | DiGeorge syndrome | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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DOID:12583 | velocardiofacial syndrome | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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DOID:5419 | schizophrenia | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:6000 | congestive heart failure | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:9993 | hypoglycemia | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:9970 | obesity | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:9351 | diabetes mellitus | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:11716 | prediabetes syndrome | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:1459 | hypothyroidism | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:10763 | hypertension | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:9743 | diabetic neuropathy | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:7998 | hyperthyroidism | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:4247 | coronary restenosis | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:10763 | hypertension | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:783 | end stage renal disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:3407 | carotid artery disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:9452 | steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:6000 | congestive heart failure | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:9970 | obesity | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:1459 | hypothyroidism | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:9743 | diabetic neuropathy | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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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