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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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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 | July 29, 2024 |
| Disease ID ▲ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080081 | nonsyndromic congenital nail disorder 3 | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:0080101 | Compton-North congenital myopathy | HGNC:2171 | Homo sapiens (human) | 1272 | CNTN1 |
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| DOID:0080108 | myoglobinuria | RGD:3313 | Rattus norvegicus (Norway rat) | 24959 | Pgam2 |
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| DOID:0080108 | myoglobinuria | HGNC:8889 | Homo sapiens (human) | 5224 | PGAM2 |
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| DOID:0080108 | myoglobinuria | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0080108 | myoglobinuria | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0080108 | myoglobinuria | MGI:1933118 | Mus musculus (house mouse) | 56012 | Pgam2 |
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| DOID:0080108 | myoglobinuria | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:0080108 | myoglobinuria | SGD:S000001635 | Saccharomyces cerevisiae S288C | 853705 | GPM1 |
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| DOID:0080109 | infantile myofibromatosis | FB:FBgn0004647 | Drosophila melanogaster (fruit fly) | 31293 | N | CG3936 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | RGD:1305756 | Rattus norvegicus (Norway rat) | 315219 | Tymp |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | HGNC:11448 | Homo sapiens (human) | 8803 | SUCLA2 |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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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: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 | HGNC:8957 | Homo sapiens (human) | 5277 | 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 | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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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: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 | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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