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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
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:182 | calcinosis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:4448 | macular degeneration | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:10126 | keratoconus | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0111535 | progressive osseous heteroplasia | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0080015 | physical disorder | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:13374 | fibrodysplasia ossificans progressiva | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:4450 | renal cell carcinoma | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0050651 | atrioventricular septal defect | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0111805 | syndromic microphthalmia 6 | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:11963 | esophagitis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:1882 | atrial heart septal defect | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:18 | urinary system disease | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:1222 | cartilage disease | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:1909 | melanoma | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0080205 | CAKUT | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0110122 | Axenfeld-Rieger syndrome type 3 | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:13976 | peptic esophagitis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:1826 | epilepsy | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0080313 | cleft palate-lateral synechia syndrome | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:540 | strabismus | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0060438 | Cole-Carpenter syndrome | HGNC:10706 | Homo sapiens (human) | 9871 | SEC24D |
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| DOID:0081003 | Cowden syndrome 7 | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0070307 | craniolenticulosutural dysplasia | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0111401 | congenital dyserythropoietic anemia type II | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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