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:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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DOID:13241 | Behcet's disease | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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DOID:3146 | lipid metabolism disorder | HGNC:2859 | Homo sapiens (human) | 1718 | DHCR24 |
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DOID:4194 | glucose metabolism disease | HGNC:2853 | Homo sapiens (human) | 1608 | DGKG |
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DOID:0080388 | nephrotic syndrome type 7 | HGNC:2852 | Homo sapiens (human) | 8526 | DGKE |
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DOID:0050561 | Lennox-Gastaut syndrome | HGNC:2851 | Homo sapiens (human) | 8527 | DGKD |
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DOID:4194 | glucose metabolism disease | HGNC:2850 | Homo sapiens (human) | 1607 | DGKB |
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DOID:4194 | glucose metabolism disease | HGNC:2849 | Homo sapiens (human) | 1606 | DGKA |
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DOID:784 | chronic kidney disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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DOID:10787 | premature menopause | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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DOID:784 | chronic kidney disease | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:1184 | nephrotic syndrome | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:0050700 | cardiomyopathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:9970 | obesity | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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DOID:784 | chronic kidney disease | SGD:S000005771 | Saccharomyces cerevisiae S288C | 854419 | DGA1 |
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DOID:9452 | steatotic liver disease | SGD:S000005771 | Saccharomyces cerevisiae S288C | 854419 | DGA1 |
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DOID:10787 | premature menopause | SGD:S000005771 | Saccharomyces cerevisiae S288C | 854419 | DGA1 |
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DOID:10140 | dry eye syndrome | SGD:S000005771 | Saccharomyces cerevisiae S288C | 854419 | DGA1 |
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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