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:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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DOID:0081017 | congenital fibrosis of the extraocular muscles 3A | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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DOID:0110082 | arrhythmogenic right ventricular dysplasia 11 | HGNC:3036 | Homo sapiens (human) | 1824 | DSC2 |
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DOID:5844 | myocardial infarction | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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DOID:0110147 | Bartter disease type 5 | HGNC:16353 | Homo sapiens (human) | 10916 | MAGED2 |
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DOID:11336 | rhinoscleroma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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DOID:0050591 | tooth agenesis | HGNC:17655 | Homo sapiens (human) | 64388 | GREM2 |
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DOID:13544 | low tension glaucoma | HGNC:7610 | Homo sapiens (human) | 4653 | MYOC |
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DOID:0111479 | combined oxidative phosphorylation deficiency 8 | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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DOID:9352 | type 2 diabetes mellitus | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
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DOID:3181 | oligodendroglioma | HGNC:9884 | Homo sapiens (human) | 5925 | RB1 |
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DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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DOID:9256 | colorectal cancer | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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DOID:0080446 | developmental and epileptic encephalopathy 66 | HGNC:23794 | Homo sapiens (human) | 23241 | PACS2 |
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DOID:0060931 | developmental dysplasia of the hip 1 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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DOID:1485 | cystic fibrosis | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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DOID:0110899 | inflammatory bowel disease 28 | HGNC:5964 | Homo sapiens (human) | 3587 | IL10RA |
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DOID:0112142 | retinitis pigmentosa 85 | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:7551 | Homo sapiens (human) | 4607 | MYBPC3 |
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DOID:10652 | Alzheimer's disease | HGNC:9205 | Homo sapiens (human) | 5445 | PON2 |
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DOID:3181 | oligodendroglioma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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DOID:9146 | visceral leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0080415 | developmental and epileptic encephalopathy 23 | HGNC:19190 | Homo sapiens (human) | 85440 | DOCK7 |
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DOID:3310 | atopic dermatitis | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024