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:0080322 | polycystic kidney disease | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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DOID:2841 | asthma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:11612 | polycystic ovary syndrome | HGNC:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
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DOID:2018 | hyperinsulinism | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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DOID:12894 | Sjogren's syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:3021 | acute kidney failure | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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DOID:0110429 | dilated cardiomyopathy 1H | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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DOID:3070 | high grade glioma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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DOID:14330 | Parkinson's disease | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
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DOID:3138 | acanthosis nigricans | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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DOID:5453 | pulmonary venoocclusive disease | HGNC:786 | Homo sapiens (human) | 468 | ATF4 |
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DOID:1909 | melanoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:684 | hepatocellular carcinoma | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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DOID:3321 | GM2 gangliosidosis | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
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DOID:162 | cancer | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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DOID:331 | central nervous system disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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DOID:10584 | retinitis pigmentosa | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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DOID:4608 | common bile duct neoplasm | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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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