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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | SGD:S000001231 | Saccharomyces cerevisiae S288C | 856595 | GPI16 |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | MGI:1926178 | Mus musculus (house mouse) | 78928 | Pigt |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | Xenbase:XB-GENE-6485976 | Xenopus laevis (African clawed frog) | 108707921 | piga.L |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | SGD:S000001648 | Saccharomyces cerevisiae S288C | 853690 | MCD4 |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | WB:WBGene00021840 | Caenorhabditis elegans | 171881 | pign-1 |
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| DOID:0080137 | multiple endocrine neoplasia type 4 | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:0080137 | multiple endocrine neoplasia type 4 | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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| DOID:0080136 | multiple mitochondrial dysfunctions syndrome 4 | HGNC:19857 | Homo sapiens (human) | 122961 | ISCA2 |
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| DOID:0080135 | multiple mitochondrial dysfunctions syndrome 3 | HGNC:27302 | Homo sapiens (human) | 200205 | IBA57 |
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| DOID:0080133 | multiple mitochondrial dysfunctions syndrome 1 | HGNC:16287 | Homo sapiens (human) | 27247 | NFU1 |
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| DOID:0080133 | multiple mitochondrial dysfunctions syndrome 1 | MGI:1913290 | Mus musculus (house mouse) | 56748 | Nfu1 |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080131 | mitochondrial DNA depletion syndrome 13 | HGNC:13601 | Homo sapiens (human) | 26235 | FBXL4 |
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| DOID:0080130 | mitochondrial DNA depletion syndrome 12a | MGI:1353495 | Mus musculus (house mouse) | 11739 | Slc25a4 |
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| DOID:0080130 | mitochondrial DNA depletion syndrome 12a | RGD:620352 | Rattus norvegicus (Norway rat) | 85333 | Slc25a4 |
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