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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:0080322 | polycystic kidney disease | HGNC:6319 | Homo sapiens (human) | 11127 | KIF3A |
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| DOID:1934 | dysostosis | HGNC:6319 | Homo sapiens (human) | 11127 | KIF3A |
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| DOID:10325 | silicosis | HGNC:6319 | Homo sapiens (human) | 11127 | KIF3A |
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| DOID:9256 | colorectal cancer | HGNC:9682 | Homo sapiens (human) | 11122 | PTPRT |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:9682 | Homo sapiens (human) | 11122 | PTPRT |
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| DOID:5419 | schizophrenia | MGI:2148258 | Mus musculus (house mouse) | 111174 | Taar1 |
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| DOID:0081399 | autosomal dominant distal hereditary motor neuronopathy 10 | HGNC:19880 | Homo sapiens (human) | 11117 | EMILIN1 |
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| DOID:0081292 | traumatic brain injury | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0070288 | primary autosomal recessive microcephaly 17 | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:10907 | microcephaly | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:11832 | visual epilepsy | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0070297 | primary microcephaly | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:1826 | epilepsy | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:9252 | amino acid metabolic disorder | HGNC:4907 | Homo sapiens (human) | 11112 | HIBADH |
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| DOID:1793 | pancreatic cancer | HGNC:1925 | Homo sapiens (human) | 1111 | CHEK1 |
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| DOID:14330 | Parkinson's disease | HGNC:236 | Homo sapiens (human) | 111 | ADCY5 |
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| DOID:10763 | hypertension | HGNC:236 | Homo sapiens (human) | 111 | ADCY5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:236 | Homo sapiens (human) | 111 | ADCY5 |
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| DOID:0111870 | nonphotosensitive trichothiodystrophy 7 | MGI:106314 | Mus musculus (house mouse) | 110960 | Tars1 |
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| DOID:9252 | amino acid metabolic disorder | MGI:106314 | Mus musculus (house mouse) | 110960 | Tars1 |
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| DOID:0111867 | nonphotosensitive trichothiodystrophy | MGI:106314 | Mus musculus (house mouse) | 110960 | Tars1 |
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| DOID:8398 | osteoarthritis | HGNC:221 | Homo sapiens (human) | 11096 | ADAMTS5 |
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| DOID:90 | degenerative disc disease | HGNC:221 | Homo sapiens (human) | 11096 | ADAMTS5 |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:221 | Homo sapiens (human) | 11096 | ADAMTS5 |
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| DOID:7148 | rheumatoid arthritis | HGNC:221 | Homo sapiens (human) | 11096 | ADAMTS5 |
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