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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:438 | autoimmune disease of the nervous system | WB:WBGene00017166 | Caenorhabditis elegans | 175827 | aldo-2 |
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| DOID:438 | autoimmune disease of the nervous system | MGI:101863 | Mus musculus (house mouse) | 11676 | Aldoc |
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| DOID:2048 | autoimmune hepatitis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:2048 | autoimmune hepatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2048 | autoimmune hepatitis | HGNC:4606 | Homo sapiens (human) | 2923 | PDIA3 |
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| DOID:2048 | autoimmune hepatitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:2048 | autoimmune hepatitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:2048 | autoimmune hepatitis | MGI:106675 | Mus musculus (house mouse) | 11450 | Adipoq |
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| DOID:7188 | autoimmune thyroiditis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:898 | autosomal dominant polycystic kidney disease | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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