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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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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:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0050700 | cardiomyopathy | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:0070166 | spermatogenic failure 20 | HGNC:25631 | Homo sapiens (human) | 55779 | CFAP44 |
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| DOID:4154 | dentinogenesis imperfecta | HGNC:3054 | Homo sapiens (human) | 1834 | DSPP |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:2841 | asthma | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:0110017 | age related macular degeneration 4 | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0060866 | patterned macular dystrophy 1 | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:12800 | mucopolysaccharidosis VI | RGD:2158 | Rattus norvegicus (Norway rat) | 25227 | Arsb |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:3343 | glycoproteinosis | HGNC:13356 | Homo sapiens (human) | 57192 | MCOLN1 |
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| DOID:9970 | obesity | HGNC:4324 | Homo sapiens (human) | 2740 | GLP1R |
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| DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0111809 | syndromic microphthalmia 2 | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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| DOID:0110390 | retinitis pigmentosa 1 | HGNC:10263 | Homo sapiens (human) | 6101 | RP1 |
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| DOID:9970 | obesity | HGNC:9076 | Homo sapiens (human) | 5346 | PLIN1 |
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| DOID:10763 | hypertension | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:850 | lung disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0110636 | congenital merosin-deficient muscular dystrophy 1A | HGNC:6482 | Homo sapiens (human) | 3908 | LAMA2 |
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| DOID:3650 | lactic acidosis | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:8398 | osteoarthritis | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080442 | developmental and epileptic encephalopathy 41 | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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