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:2841 | asthma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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DOID:14451 | hyperkalemic periodic paralysis | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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DOID:9744 | type 1 diabetes mellitus | MGI:96572 | Mus musculus (house mouse) | 16333 | Ins1 |
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DOID:9744 | type 1 diabetes mellitus | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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DOID:2512 | nevoid basal cell carcinoma syndrome | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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DOID:4989 | pancreatitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:10763 | hypertension | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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DOID:9266 | cystinuria | MGI:1195264 | Mus musculus (house mouse) | 20532 | Slc3a1 |
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DOID:1094 | attention deficit hyperactivity disorder | HGNC:11049 | Homo sapiens (human) | 6531 | SLC6A3 |
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DOID:0080199 | colorectal carcinoma | RGD:2311 | Rattus norvegicus (Norway rat) | 25407 | Cd59b |
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DOID:0080199 | colorectal carcinoma | HGNC:1689 | Homo sapiens (human) | 966 | CD59 |
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DOID:6000 | congestive heart failure | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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DOID:3328 | temporal lobe epilepsy | HGNC:4845 | Homo sapiens (human) | 348980 | HCN1 |
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DOID:3328 | temporal lobe epilepsy | RGD:620688 | Rattus norvegicus (Norway rat) | 84390 | Hcn1 |
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DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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DOID:0111113 | nephronophthisis 2 | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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DOID:0111114 | nephronophthisis 3 | HGNC:7907 | Homo sapiens (human) | 27031 | NPHP3 |
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DOID:1067 | open-angle glaucoma | HGNC:7610 | Homo sapiens (human) | 4653 | MYOC |
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DOID:3393 | coronary artery disease | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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DOID:14330 | Parkinson's disease | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
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DOID:1682 | congenital heart disease | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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DOID:9970 | obesity | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | MGI:1194506 | Mus musculus (house mouse) | 20713 | Serpini1 |
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DOID:10933 | obsessive-compulsive disorder | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:784 | chronic kidney disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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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