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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:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:1324 | lung cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:14695 | galactokinase deficiency | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:0111391 | mucopolysaccharidosis IVA | HGNC:4122 | Homo sapiens (human) | 2588 | GALNS |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0111069 | congenital bile acid synthesis defect 2 | HGNC:388 | Homo sapiens (human) | 6718 | AKR1D1 |
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| DOID:0111680 | essential fructosuria | HGNC:6315 | Homo sapiens (human) | 3795 | KHK |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:0081221 | autosomal recessive intellectual developmental disorder 59 | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0050793 | short QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:0060585 | Noonan syndrome 7 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:4621 | holoprosencephaly | HGNC:29185 | Homo sapiens (human) | 23007 | PLCH1 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:9970 | obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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