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 | July 29, 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:4450 | renal cell carcinoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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DOID:5844 | myocardial infarction | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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DOID:0050742 | nicotine dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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DOID:3717 | gastric adenocarcinoma | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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DOID:0111390 | mucopolysaccharidosis Ih | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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DOID:3082 | interstitial lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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DOID:10763 | hypertension | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:3021 | acute kidney failure | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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DOID:1074 | kidney failure | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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DOID:0050855 | renal fibrosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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DOID:1459 | hypothyroidism | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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DOID:1508 | candidiasis | HGNC:4015 | Homo sapiens (human) | 2526 | FUT4 |
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DOID:14250 | Down syndrome | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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DOID:9408 | acute myocardial infarction | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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DOID:9352 | type 2 diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:3082 | interstitial lung disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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DOID:8577 | ulcerative colitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:1380 | endometrial cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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DOID:10283 | prostate cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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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 v4.0.0
Last updated: August 19, 2024