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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:820 | myocarditis | HGNC:14900 | Homo sapiens (human) | 50616 | IL22 |
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| DOID:399 | tuberculosis | HGNC:14900 | Homo sapiens (human) | 50616 | IL22 |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:0050784 | primary progressive multiple sclerosis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:8398 | osteoarthritis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:9256 | colorectal cancer | HGNC:14897 | Homo sapiens (human) | 80271 | ITPKC |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:14896 | Homo sapiens (human) | 57731 | SPTBN4 |
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| DOID:90 | degenerative disc disease | HGNC:14872 | Homo sapiens (human) | 54829 | ASPN |
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| DOID:8398 | osteoarthritis | HGNC:14872 | Homo sapiens (human) | 54829 | ASPN |
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| DOID:7147 | ankylosing spondylitis | HGNC:14872 | Homo sapiens (human) | 54829 | ASPN |
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| DOID:557 | kidney disease | HGNC:14868 | Homo sapiens (human) | 80833 | APOL3 |
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| DOID:9743 | diabetic neuropathy | HGNC:14866 | Homo sapiens (human) | 64399 | HHIP |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14866 | Homo sapiens (human) | 64399 | HHIP |
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| DOID:12236 | primary biliary cholangitis | HGNC:14866 | Homo sapiens (human) | 64399 | HHIP |
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| DOID:1508 | candidiasis | HGNC:14860 | Homo sapiens (human) | 23190 | UBXN4 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:9884 | muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:1059 | intellectual disability | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110821 | hereditary spastic paraplegia 76 | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:9970 | obesity | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
|
