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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:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | FB:FBgn0028916 | Drosophila melanogaster (fruit fly) | 34835 | CG33090 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | MGI:2654325 | Mus musculus (house mouse) | 230101 | Gba2 |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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| DOID:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:0110858 | polycystic kidney disease 1 | RGD:3130 | Rattus norvegicus (Norway rat) | 24577 | Myc |
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| DOID:0110858 | polycystic kidney disease 1 | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0110860 | polycystic kidney disease 3 | MGI:1097667 | Mus musculus (house mouse) | 14376 | Ganab |
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| DOID:0110860 | polycystic kidney disease 3 | SGD:S000000433 | Saccharomyces cerevisiae S288C | 852530 | ROT2 |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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