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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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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:3883 | Lynch syndrome | HGNC:6759 | Homo sapiens (human) | 4082 | MARCKS |
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| DOID:0110177 | Charcot-Marie-Tooth disease axonal type 2N | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:0080046 | Stickler syndrome | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0070474 | childhood-onset neurodegeneration with brain atrophy | HGNC:12511 | Homo sapiens (human) | 7343 | UBTF |
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| DOID:5844 | myocardial infarction | HGNC:8744 | Homo sapiens (human) | 5126 | PCSK2 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:3307 | teratoma | HGNC:7850 | Homo sapiens (human) | 4831 | NME2 |
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| DOID:14040 | autoimmune polyendocrine syndrome | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:9976 | heroin dependence | HGNC:5297 | Homo sapiens (human) | 3359 | HTR3A |
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| DOID:0110573 | autosomal dominant nonsyndromic deafness 4A | HGNC:23212 | Homo sapiens (human) | 79784 | MYH14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:7884 | Homo sapiens (human) | 4855 | NOTCH4 |
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| DOID:9245 | Alagille syndrome | HGNC:7882 | Homo sapiens (human) | 4853 | NOTCH2 |
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| DOID:2377 | multiple sclerosis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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| DOID:9256 | colorectal cancer | HGNC:6844 | Homo sapiens (human) | 6416 | MAP2K4 |
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| DOID:0081125 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 | HGNC:15870 | Homo sapiens (human) | 55969 | RAB5IF |
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| DOID:0070082 | schizophrenia 6 | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:0060428 | SATB2-associated syndrome | HGNC:21637 | Homo sapiens (human) | 23314 | SATB2 |
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| DOID:13025 | retinopathy of prematurity | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:11181 | Homo sapiens (human) | 6649 | SOD3 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:7147 | ankylosing spondylitis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:4450 | renal cell carcinoma | HGNC:700 | Homo sapiens (human) | 405 | ARNT |
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| DOID:4549 | extraskeletal myxoid chondrosarcoma | HGNC:7982 | Homo sapiens (human) | 8013 | NR4A3 |
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| DOID:218 | ascending colon cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
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