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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:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:5294 | Homo sapiens (human) | 3357 | HTR2B |
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| DOID:9743 | diabetic neuropathy | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:12849 | autistic disorder | HGNC:20653 | Homo sapiens (human) | 285195 | SLC9A9 |
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| DOID:231 | motor neuron disease | HGNC:11571 | Homo sapiens (human) | 23435 | TARDBP |
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| DOID:11252 | microcytic anemia | HGNC:16517 | Homo sapiens (human) | 164656 | TMPRSS6 |
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| DOID:3393 | coronary artery disease | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:9256 | colorectal cancer | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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| DOID:10123 | pigmentation disease | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:1928 | Williams-Beuren syndrome | HGNC:4041 | Homo sapiens (human) | 7976 | FZD3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:11199 | hypoparathyroidism | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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| DOID:5419 | schizophrenia | HGNC:3024 | Homo sapiens (human) | 1814 | DRD3 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
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| DOID:2377 | multiple sclerosis | HGNC:7215 | Homo sapiens (human) | 10198 | MPHOSPH9 |
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| DOID:12134 | factor VIII deficiency | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:12177 | common variable immunodeficiency | HGNC:17642 | Homo sapiens (human) | 64421 | DCLRE1C |
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| DOID:1115 | sarcoma | HGNC:9665 | Homo sapiens (human) | 5787 | PTPRB |
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| DOID:9669 | senile cataract | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:655 | inherited metabolic disorder | HGNC:19331 | Homo sapiens (human) | 326625 | MMAB |
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| DOID:12361 | Graves' disease | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:3393 | coronary artery disease | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:3012 | Homo sapiens (human) | 1806 | DPYD |
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| DOID:0111808 | linear skin defects with multiple congenital anomalies 1 | HGNC:4837 | Homo sapiens (human) | 3052 | HCCS |
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| DOID:10283 | prostate cancer | HGNC:11458 | Homo sapiens (human) | 6822 | SULT2A1 |
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