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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:3083 | chronic obstructive pulmonary disease | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:0112104 | Sotos syndrome 3 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0110909 | inflammatory bowel disease 25 | HGNC:5965 | Homo sapiens (human) | 3588 | IL10RB |
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| DOID:0080199 | colorectal carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1574 | alcohol use disorder | HGNC:6833 | Homo sapiens (human) | 4128 | MAOA |
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| DOID:0110796 | hereditary spastic paraplegia 44 | HGNC:17494 | Homo sapiens (human) | 57165 | GJC2 |
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| DOID:4428 | dyslexia | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0080820 | occupational asthma | HGNC:4936 | Homo sapiens (human) | 3111 | HLA-DOA |
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| DOID:3652 | Leigh disease | HGNC:7461 | Homo sapiens (human) | 4540 | ND5 |
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| DOID:3393 | coronary artery disease | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:446 | primary hyperaldosteronism | HGNC:6266 | Homo sapiens (human) | 3762 | KCNJ5 |
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| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0080162 | lupus nephritis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0080676 | Stickler syndrome 1 | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080000 | muscular disease | HGNC:6143 | Homo sapiens (human) | 3679 | ITGA7 |
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| DOID:9256 | colorectal cancer | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0090137 | complex cortical dysplasia with other brain malformations 1 | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:1470 | major depressive disorder | HGNC:2516 | Homo sapiens (human) | 1501 | CTNND2 |
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| DOID:0111608 | distal arthrogryposis type 5 | HGNC:26270 | Homo sapiens (human) | 63895 | PIEZO2 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:11905 | Homo sapiens (human) | 8795 | TNFRSF10B |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:1287 | cardiovascular system disease | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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