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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:0070280 | primary autosomal recessive microcephaly 5 | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:0081386 | TANGO2-related metabolic encephalopathy and arrythmias | HGNC:25439 | Homo sapiens (human) | 128989 | TANGO2 |
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| DOID:0110958 | Gaucher's disease type II | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:4183 | pseudopseudohypoparathyroidism | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0110336 | osteogenesis imperfecta type 8 | HGNC:19316 | Homo sapiens (human) | 64175 | P3H1 |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0111020 | cone-rod dystrophy 9 | HGNC:216 | Homo sapiens (human) | 8754 | ADAM9 |
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| DOID:0050773 | paraganglioma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0110326 | hypertrophic cardiomyopathy 20 | HGNC:29557 | Homo sapiens (human) | 91624 | NEXN |
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| DOID:0110383 | retinitis pigmentosa 7 | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:9269 | maple syrup urine disease | HGNC:2698 | Homo sapiens (human) | 1629 | DBT |
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| DOID:0110863 | congenital stationary night blindness autosomal dominant 2 | HGNC:8786 | Homo sapiens (human) | 5158 | PDE6B |
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| DOID:0110995 | Joubert syndrome 26 | HGNC:29068 | Homo sapiens (human) | 23247 | KATNIP |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:0110448 | dilated cardiomyopathy 1HH | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0060196 | amyotrophic lateral sclerosis type 4 | HGNC:445 | Homo sapiens (human) | 23064 | SETX |
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| DOID:11836 | clubfoot | HGNC:9004 | Homo sapiens (human) | 5307 | PITX1 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:2435 | Homo sapiens (human) | 1438 | CSF2RA |
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| DOID:0111044 | gray platelet syndrome | HGNC:31928 | Homo sapiens (human) | 23218 | NBEAL2 |
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| DOID:0110871 | congenital stationary night blindness 2A | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0050755 | spinocerebellar ataxia with axonal neuropathy 2 | HGNC:445 | Homo sapiens (human) | 23064 | SETX |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0070378 | developmental and epileptic encephalopathy 109 | HGNC:24824 | Homo sapiens (human) | 51343 | FZR1 |
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| DOID:0060793 | hypomyelinating leukodystrophy 5 | HGNC:24587 | Homo sapiens (human) | 84668 | HYCC1 |
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