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:0080297 | Coffin-Siris syndrome 6 | HGNC:18037 | Homo sapiens (human) | 196528 | ARID2 |
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DOID:12704 | ataxia telangiectasia | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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DOID:0060837 | isolated microphthalmia 5 | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
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DOID:1307 | dementia | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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DOID:0080447 | developmental and epileptic encephalopathy 43 | HGNC:4083 | Homo sapiens (human) | 2562 | GABRB3 |
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DOID:4947 | cholangiocarcinoma | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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DOID:1319 | brain cancer | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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DOID:13241 | Behcet's disease | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:4448 | macular degeneration | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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DOID:0112056 | X-linked intellectual disability-short stature-overweight syndrome | HGNC:19073 | Homo sapiens (human) | 57187 | THOC2 |
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DOID:0070114 | Niemann-Pick disease type C2 | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
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DOID:1883 | hepatitis C | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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DOID:0111640 | autosomal recessive nonsyndromic deafness 111 | HGNC:3496 | Homo sapiens (human) | 10205 | MPZL2 |
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DOID:12361 | Graves' disease | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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DOID:10923 | sickle cell anemia | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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DOID:0060669 | cerebral cavernous malformation | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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DOID:0110652 | long QT syndrome 11 | HGNC:379 | Homo sapiens (human) | 10142 | AKAP9 |
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DOID:0050773 | paraganglioma | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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DOID:11984 | hypertrophic cardiomyopathy | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:6647 | Homo sapiens (human) | 25802 | LMOD1 |
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DOID:1793 | pancreatic cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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DOID:1307 | dementia | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
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DOID:0111076 | progressive familial heart block type IB | HGNC:17993 | Homo sapiens (human) | 54795 | TRPM4 |
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DOID:417 | autoimmune disease | HGNC:18187 | Homo sapiens (human) | 54414 | SIAE |
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DOID:6432 | pulmonary hypertension | HGNC:9611 | Homo sapiens (human) | 5747 | PTK2 |
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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