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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB ▼ | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:11721 | glycogen storage disease VII | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:13129 | severe pre-eclampsia | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:8778 | Crohn's disease | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:6000 | congestive heart failure | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | SGD:S000003904 | Saccharomyces cerevisiae S288C | 853608 | PMT4 |
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| DOID:0110658 | congenital myasthenic syndrome 15 | ZFIN:ZDB-GENE-041010-195 | Danio rerio (zebrafish) | 450072 | alg14 |
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| DOID:1040 | chronic lymphocytic leukemia | RGD:3130 | Rattus norvegicus (Norway rat) | 24577 | Myc |
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| DOID:11832 | visual epilepsy | RGD:620103 | Rattus norvegicus (Norway rat) | 64639 | Bad |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:1035 | aggressive NK-cell leukemia | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1591 | renovascular hypertension | MGI:105977 | Mus musculus (house mouse) | 14380 | G6pd2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | Xenbase:XB-GENE-17345473 | Xenopus laevis (African clawed frog) | 444674 | mgat2.S |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:2043 | hepatitis B | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0060180 | colitis | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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| DOID:767 | muscular atrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1793 | pancreatic cancer | MGI:1202879 | Mus musculus (house mouse) | 21416 | Tcf7l2 |
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| DOID:12053 | cryptococcosis | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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