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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:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:10652 | Alzheimer's disease | HGNC:1834 | Homo sapiens (human) | 1051 | CEBPB |
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| DOID:7148 | rheumatoid arthritis | HGNC:1834 | Homo sapiens (human) | 1051 | CEBPB |
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| DOID:2256 | osteochondrodysplasia | HGNC:1834 | Homo sapiens (human) | 1051 | CEBPB |
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| DOID:934 | viral infectious disease | HGNC:1834 | Homo sapiens (human) | 1051 | CEBPB |
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| DOID:684 | hepatocellular carcinoma | HGNC:1834 | Homo sapiens (human) | 1051 | CEBPB |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1820 | Homo sapiens (human) | 1088 | CEACAM8 |
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| DOID:0110573 | autosomal dominant nonsyndromic deafness 4A | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0111636 | autosomal recessive nonsyndromic deafness 113 | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0110574 | autosomal dominant nonsyndromic deafness 4B | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0050700 | cardiomyopathy | FB:FBgn0039774 | Drosophila melanogaster (fruit fly) | 43618 | CDase |
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| DOID:1826 | epilepsy | HGNC:1811 | Homo sapiens (human) | 9425 | CDYL |
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| DOID:987 | alopecia | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:3310 | atopic dermatitis | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:0110699 | hypotrichosis 2 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:0070520 | peeling skin syndrome 1 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:162 | cancer | HGNC:1801 | Homo sapiens (human) | 8760 | CDS2 |
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| DOID:162 | cancer | HGNC:1800 | Homo sapiens (human) | 1040 | CDS1 |
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| DOID:162 | cancer | SGD:S000000233 | Saccharomyces cerevisiae S288C | 852317 | CDS1 |
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| DOID:0110877 | holoprosencephaly 11 | HGNC:17104 | Homo sapiens (human) | 50937 | CDON |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:9119 | acute myeloid leukemia | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:1612 | breast cancer | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:2671 | transitional cell carcinoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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