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:11612 | polycystic ovary syndrome | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:9452 | steatotic liver disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:12361 | Graves' disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:1070 | primary open angle glaucoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:9352 | type 2 diabetes mellitus | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:2048 | autoimmune hepatitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:8947 | diabetic retinopathy | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:1612 | breast cancer | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:3083 | chronic obstructive pulmonary disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:13207 | proliferative diabetic retinopathy | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:0050847 | sleep apnea | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:7147 | ankylosing spondylitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:0060180 | colitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:0050830 | peripheral artery disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:13241 | Behcet's disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:7998 | hyperthyroidism | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:1936 | atherosclerosis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:13378 | Kawasaki disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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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