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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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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:0110084 | arrhythmogenic right ventricular dysplasia 13 | HGNC:2511 | Homo sapiens (human) | 29119 | CTNNA3 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:3296 | Homo sapiens (human) | 1981 | EIF4G1 |
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| DOID:2590 | familial nephrotic syndrome | HGNC:18143 | Homo sapiens (human) | 23500 | DAAM2 |
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| DOID:0110050 | Alzheimer's disease 18 | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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| DOID:9256 | colorectal cancer | HGNC:3373 | Homo sapiens (human) | 2033 | EP300 |
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| DOID:4586 | familial meningioma | HGNC:11109 | Homo sapiens (human) | 6605 | SMARCE1 |
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| DOID:0070301 | multiple epiphyseal dysplasia 6 | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:0080454 | developmental and epileptic encephalopathy 42 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:11537 | Homo sapiens (human) | 6874 | TAF4 |
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| DOID:9256 | colorectal cancer | HGNC:2897 | Homo sapiens (human) | 10395 | DLC1 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0110409 | retinitis pigmentosa 46 | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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| DOID:0090134 | complex cortical dysplasia with other brain malformations 3 | HGNC:6318 | Homo sapiens (human) | 3796 | KIF2A |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0080988 | pretibial dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:0080465 | developmental and epileptic encephalopathy 30 | HGNC:11142 | Homo sapiens (human) | 150094 | SIK1 |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:4888 | Homo sapiens (human) | 3078 | CFHR1 |
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| DOID:0081342 | congenital myopathy 8 | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:0080621 | glucocorticoid deficiency 1 | HGNC:6930 | Homo sapiens (human) | 4158 | MC2R |
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| DOID:0112010 | pituitary adenoma 3 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0090082 | hypogonadotropic hypogonadism 20 with or without anosmia | HGNC:3673 | Homo sapiens (human) | 8822 | FGF17 |
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| DOID:0111861 | Meester-Loeys syndrome | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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