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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:0090068 | giant axonal neuropathy 1 | HGNC:4137 | Homo sapiens (human) | 8139 | GAN |
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| DOID:0110939 | autosomal recessive osteopetrosis 5 | HGNC:21652 | Homo sapiens (human) | 28962 | OSTM1 |
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| DOID:0060798 | hypomyelinating leukodystrophy 6 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:14557 | primary pulmonary hypertension | HGNC:1078 | Homo sapiens (human) | 659 | BMPR2 |
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| DOID:0110430 | dilated cardiomyopathy 1G | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:12798 | mucopolysaccharidosis | HGNC:25239 | Homo sapiens (human) | 153642 | ARSK |
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| DOID:0110670 | congenital myasthenic syndrome 9 | HGNC:7525 | Homo sapiens (human) | 4593 | MUSK |
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| DOID:0050471 | Carney complex | HGNC:9388 | Homo sapiens (human) | 5573 | PRKAR1A |
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| DOID:0110488 | autosomal recessive nonsyndromic deafness 3 | HGNC:7594 | Homo sapiens (human) | 51168 | MYO15A |
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| DOID:0060206 | amyotrophic lateral sclerosis type 15 | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
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| DOID:0070469 | neurodevelopmental disorder with dysmorphic facies and thin corpus callosum | HGNC:11465 | Homo sapiens (human) | 11198 | SUPT16H |
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| DOID:0070295 | primary autosomal dominant microcephaly 18 | HGNC:20751 | Homo sapiens (human) | 23001 | WDFY3 |
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| DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | HGNC:8943 | Homo sapiens (human) | 5274 | SERPINI1 |
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| DOID:0090071 | hypogonadotropic hypogonadism 11 with or without anosmia | HGNC:11528 | Homo sapiens (human) | 6870 | TACR3 |
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| DOID:0060367 | Parkinson's disease 1 | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
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| DOID:0060900 | Parkinson's disease 14 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0110914 | infantile hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:9074 | systemic lupus erythematosus | HGNC:2956 | Homo sapiens (human) | 1773 | DNASE1 |
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| DOID:0110153 | Charcot-Marie-Tooth disease type 1E | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0080201 | Peters plus syndrome | HGNC:20207 | Homo sapiens (human) | 145173 | B3GLCT |
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| DOID:3320 | Tay-Sachs disease | HGNC:4878 | Homo sapiens (human) | 3073 | HEXA |
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| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:21497 | Homo sapiens (human) | 28976 | ACAD9 |
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