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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:1470 | major depressive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:0110267 | cataract 44 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:612 | primary immunodeficiency disease | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0060898 | Parkinson's disease 20 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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