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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:0110849 | xeroderma pigmentosum group G | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:0050768 | mitochondrial complex V (ATP synthase) deficiency nuclear type 1 | HGNC:18802 | Homo sapiens (human) | 91647 | ATPAF2 |
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| DOID:0110313 | hypertrophic cardiomyopathy 7 | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0060896 | Parkinson's disease 23 | HGNC:23594 | Homo sapiens (human) | 54832 | VPS13C |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:0081048 | congenital limbs-face contractures-hypotonia-developmental delay syndrome | HGNC:19082 | Homo sapiens (human) | 259232 | NALCN |
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| DOID:0090122 | aromatase excess syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0080096 | myofibrillar myopathy 5 | HGNC:3756 | Homo sapiens (human) | 2318 | FLNC |
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| DOID:0080717 | infantile liver failure syndrome 1 | HGNC:6512 | Homo sapiens (human) | 51520 | LARS1 |
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| DOID:0060757 | sclerosteosis 2 | HGNC:6696 | Homo sapiens (human) | 4038 | LRP4 |
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| DOID:0110061 | amelogenesis imperfecta hypomaturation type 2A3 | HGNC:26790 | Homo sapiens (human) | 256764 | WDR72 |
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| DOID:0070486 | Parkinson's disease 25 | HGNC:9308 | Homo sapiens (human) | 5524 | PTPA |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0090143 | brachyolmia-amelogenesis imperfecta syndrome | HGNC:6716 | Homo sapiens (human) | 4054 | LTBP3 |
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| DOID:0080093 | myofibrillar myopathy 2 | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0111340 | dominant optic atrophy plus syndrome | HGNC:8140 | Homo sapiens (human) | 4976 | OPA1 |
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| DOID:10159 | osteonecrosis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0060895 | Parkinson's disease 4 | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:7400 | Nijmegen breakage syndrome | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
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| DOID:0070472 | early-onset epilepsy 3 | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:0060013 | X-linked severe combined immunodeficiency | HGNC:6010 | Homo sapiens (human) | 3561 | IL2RG |
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