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:3892 | insulinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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DOID:10763 | hypertension | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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DOID:6498 | seborrheic keratosis | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:9975 | cocaine dependence | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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DOID:5082 | liver cirrhosis | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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DOID:3393 | coronary artery disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:0050771 | pheochromocytoma | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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DOID:1214 | tympanosclerosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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DOID:3744 | cervical squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:12932 | endomyocardial fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:3323 | Sandhoff disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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DOID:874 | bacterial pneumonia | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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DOID:2978 | carbohydrate metabolic disorder | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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DOID:10652 | Alzheimer's disease | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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DOID:1793 | pancreatic cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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DOID:0060224 | atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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DOID:3702 | cervical adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:0050770 | polycystic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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DOID:0014667 | disease of metabolism | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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DOID:863 | nervous system disease | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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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