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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Alliance of Genome Resources
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 |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070037 | autosomal dominant intellectual developmental disorder 7 | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:0110248 | cataract 30 | HGNC:12692 | Homo sapiens (human) | 7431 | VIM |
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| DOID:9970 | obesity | HGNC:6932 | Homo sapiens (human) | 4160 | MC4R |
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| DOID:0070222 | progressive familial intrahepatic cholestasis 2 | HGNC:42 | Homo sapiens (human) | 8647 | ABCB11 |
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| DOID:6432 | pulmonary hypertension | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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| DOID:11870 | Pick's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:0090018 | autosomal dominant familial periodic fever | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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| DOID:2349 | arteriosclerosis | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:10487 | Hirschsprung's disease | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:0111160 | camptodactyly-tall stature-scoliosis-hearing loss syndrome | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:783 | end stage renal disease | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:166 | Homo sapiens (human) | 81 | ACTN4 |
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| DOID:10487 | Hirschsprung's disease | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
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| DOID:0070539 | Halperin-Birk syndrome | HGNC:17052 | Homo sapiens (human) | 22872 | SEC31A |
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| DOID:13133 | HELLP syndrome | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:2987 | familial mediterranean fever | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | HGNC:20672 | Homo sapiens (human) | 23133 | PHF8 |
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| DOID:850 | lung disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0110224 | Brugada syndrome 7 | HGNC:20665 | Homo sapiens (human) | 55800 | SCN3B |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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| DOID:0110186 | Charcot-Marie-Tooth disease type 4D | HGNC:7679 | Homo sapiens (human) | 10397 | NDRG1 |
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| DOID:1561 | cognitive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:10825 | essential hypertension | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:1929 | supravalvular aortic stenosis | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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