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:3393 | coronary artery disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:5844 | myocardial infarction | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:1612 | breast cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:2841 | asthma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:10286 | prostate carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:2349 | arteriosclerosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:13406 | pulmonary sarcoidosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:418 | systemic scleroderma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:9538 | multiple myeloma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:3371 | chondrosarcoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:0050700 | cardiomyopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:11720 | distal myopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:423 | myopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:0080095 | myofibrillar myopathy 4 | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:0081337 | congenital myopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:0110423 | dilated cardiomyopathy 1C | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:11722 | myotonic dystrophy type 1 | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:0080092 | myofibrillar myopathy 1 | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:12930 | dilated cardiomyopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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DOID:0110739 | neurodegeneration with brain iron accumulation 5 | HGNC:28912 | Homo sapiens (human) | 11152 | WDR45 |
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DOID:0090014 | severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | HGNC:2252 | Homo sapiens (human) | 11151 | CORO1A |
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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