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GlyTouCan
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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:2355 | anemia | HGNC:30142 | Homo sapiens (human) | 9518 | GDF15 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:11054 | urinary bladder cancer | HGNC:3212 | Homo sapiens (human) | 9521 | EEF1E1 |
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| DOID:9256 | colorectal cancer | HGNC:3212 | Homo sapiens (human) | 9521 | EEF1E1 |
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| DOID:10534 | stomach cancer | HGNC:3212 | Homo sapiens (human) | 9521 | EEF1E1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:10563 | Homo sapiens (human) | 9522 | SCAMP1 |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0050889 | non-syndromic intellectual disability | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0110815 | hereditary spastic paraplegia 64 | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:3213 | demyelinating disease | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:1459 | hypothyroidism | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:224 | transient cerebral ischemia | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:10591 | pre-eclampsia | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:1793 | pancreatic cancer | HGNC:940 | Homo sapiens (human) | 9530 | BAG4 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0050700 | cardiomyopathy | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0110448 | dilated cardiomyopathy 1HH | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:11832 | visual epilepsy | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:1793 | pancreatic cancer | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0080097 | myofibrillar myopathy 6 | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:3068 | glioblastoma | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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