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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:3068 | glioblastoma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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| DOID:0070041 | autosomal dominant intellectual developmental disorder 11 | HGNC:3378 | Homo sapiens (human) | 2036 | EPB41L1 |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0111532 | osteoglophonic dysplasia | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:10825 | essential hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:0110993 | Joubert syndrome 24 | HGNC:25774 | Homo sapiens (human) | 79867 | TCTN2 |
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| DOID:2226 | myeloproliferative neoplasm | HGNC:25941 | Homo sapiens (human) | 54790 | TET2 |
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| DOID:9834 | hyperopia | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:2723 | dermatitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:1927 | sphingolipidosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0070146 | hereditary sensory neuropathy type 4 | HGNC:8031 | Homo sapiens (human) | 4914 | NTRK1 |
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| DOID:10907 | microcephaly | HGNC:14409 | Homo sapiens (human) | 60386 | SLC25A19 |
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| DOID:594 | panic disorder | HGNC:6833 | Homo sapiens (human) | 4128 | MAOA |
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| DOID:11204 | allergic conjunctivitis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:0081011 | Bardet-Biedl syndrome 22 | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0050902 | medulloblastoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:10485 | Homo sapiens (human) | 6263 | RYR3 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:0081158 | dilated cardiomyopathy 1MM | HGNC:7551 | Homo sapiens (human) | 4607 | MYBPC3 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:3652 | Leigh disease | HGNC:7461 | Homo sapiens (human) | 4540 | MT-ND5 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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