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:224 | transient cerebral ischemia | HGNC:1594 | Homo sapiens (human) | 902 | CCNH |
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DOID:9970 | obesity | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:1824 | status epilepticus | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:4947 | cholangiocarcinoma | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:526 | human immunodeficiency virus infectious disease | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:0060074 | ductal carcinoma in situ | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:3008 | invasive ductal carcinoma | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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DOID:612 | primary immunodeficiency disease | HGNC:25118 | Homo sapiens (human) | 90268 | OTULIN |
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DOID:0080163 | otulipenia | HGNC:25118 | Homo sapiens (human) | 90268 | OTULIN |
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DOID:1928 | Williams-Beuren syndrome | HGNC:961 | Homo sapiens (human) | 9031 | BAZ1B |
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DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9011 | Homo sapiens (human) | 9033 | PKD2L1 |
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DOID:0110859 | polycystic kidney disease 2 | HGNC:9011 | Homo sapiens (human) | 9033 | PKD2L1 |
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DOID:11724 | limb-girdle muscular dystrophy | HGNC:19044 | Homo sapiens (human) | 90342 | FER1L5 |
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DOID:224 | transient cerebral ischemia | HGNC:18451 | Homo sapiens (human) | 90411 | MCFD2 |
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DOID:8866 | actinic keratosis | HGNC:30767 | Homo sapiens (human) | 90417 | KNSTRN |
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DOID:3151 | skin squamous cell carcinoma | HGNC:30767 | Homo sapiens (human) | 90417 | KNSTRN |
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DOID:684 | hepatocellular carcinoma | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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DOID:1380 | endometrial cancer | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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DOID:5082 | liver cirrhosis | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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DOID:574 | peripheral nervous system disease | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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DOID:1793 | pancreatic cancer | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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DOID:12689 | acoustic neuroma | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:9581 | Homo sapiens (human) | 9050 | PSTPIP2 |
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DOID:0080519 | PAPA syndrome | HGNC:9580 | Homo sapiens (human) | 9051 | PSTPIP1 |
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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