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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
UniCarb-DR
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 / OrganismsTools
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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:2841 | asthma | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:5419 | schizophrenia | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:9976 | heroin dependence | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:2841 | asthma | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:12140 | Chagas disease | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:1596 | depressive disorder | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:3312 | bipolar disorder | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:1470 | major depressive disorder | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:2841 | asthma | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:0050685 | small cell carcinoma | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:0060889 | prune belly syndrome | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:3770 | pulmonary fibrosis | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:365 | bladder disease | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:6000 | congestive heart failure | HGNC:1953 | Homo sapiens (human) | 1132 | CHRM4 |
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| DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:1574 | alcohol use disorder | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0110662 | congenital myasthenic syndrome 1B | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0081119 | benign familial infantile seizures 6 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:1574 | alcohol use disorder | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:3905 | lung carcinoma | HGNC:1957 | Homo sapiens (human) | 1136 | CHRNA3 |
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