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:7693 | abdominal aortic aneurysm | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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DOID:0110163 | Charcot-Marie-Tooth disease axonal type 2F | HGNC:5246 | Homo sapiens (human) | 3315 | HSPB1 |
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DOID:0070380 | developmental and epileptic encephalopathy 85 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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DOID:850 | lung disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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DOID:10941 | intracranial aneurysm | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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DOID:3910 | lung adenocarcinoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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DOID:10316 | pneumoconiosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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DOID:9884 | muscular dystrophy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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DOID:0112307 | sarcosinemia | HGNC:10536 | Homo sapiens (human) | 1757 | SARDH |
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DOID:1037 | lymphoid leukemia | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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DOID:13406 | pulmonary sarcoidosis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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DOID:437 | myasthenia gravis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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DOID:1574 | alcohol use disorder | HGNC:2082 | Homo sapiens (human) | 9575 | CLOCK |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:24276 | Homo sapiens (human) | 25813 | SAMM50 |
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DOID:0090086 | hypogonadotropic hypogonadism 6 with or without anosmia | HGNC:3686 | Homo sapiens (human) | 2253 | FGF8 |
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DOID:12700 | hyperprolactinemia | HGNC:8910 | Homo sapiens (human) | 5241 | PGR |
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DOID:9074 | systemic lupus erythematosus | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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DOID:0060575 | 3MC syndrome 1 | HGNC:6901 | Homo sapiens (human) | 5648 | MASP1 |
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DOID:0081363 | distal myopathy with rimmed vacuoles | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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DOID:14067 | Plasmodium falciparum malaria | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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DOID:9974 | drug dependence | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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DOID:10322 | berylliosis | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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DOID:2256 | osteochondrodysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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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