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 |
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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 |
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DOID:0080520 | Tn polyagglutination syndrome | WB:WBGene00015861 | Caenorhabditis elegans | 182687 | C16D9.6 |
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DOID:0050667 | alcohol-related neurodevelopmental disorder | WB:WBGene00015800 | Caenorhabditis elegans | 182643 | C15H9.4 |
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DOID:1459 | hypothyroidism | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0111042 | glycogen storage disease IXa | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0050545 | visceral heterotaxy | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:2747 | glycogen storage disease | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:824 | periodontitis | WB:WBGene00015545 | Caenorhabditis elegans | 181720 | C06G1.1 |
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DOID:9970 | obesity | WB:WBGene00015545 | Caenorhabditis elegans | 181720 | C06G1.1 |
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DOID:5082 | liver cirrhosis | WB:WBGene00015545 | Caenorhabditis elegans | 181720 | C06G1.1 |
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DOID:13603 | obstructive jaundice | WB:WBGene00015545 | Caenorhabditis elegans | 181720 | C06G1.1 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00015353 | Caenorhabditis elegans | 3565859 | C02F5.13 |
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DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | MGI:1346013 | Mus musculus (house mouse) | 23828 | Bves |
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DOID:6419 | tetralogy of Fallot | MGI:1346013 | Mus musculus (house mouse) | 23828 | Bves |
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DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | RGD:1561100 | Rattus norvegicus (Norway rat) | 365603 | Bves |
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DOID:6419 | tetralogy of Fallot | RGD:1561100 | Rattus norvegicus (Norway rat) | 365603 | Bves |
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DOID:162 | cancer | MGI:1343463 | Mus musculus (house mouse) | 12237 | Bub3 |
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DOID:0070296 | primary autosomal recessive microcephaly | MGI:1100510 | Mus musculus (house mouse) | 12235 | Bub1 |
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DOID:9256 | colorectal cancer | MGI:1100510 | Mus musculus (house mouse) | 12235 | Bub1 |
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DOID:10322 | berylliosis | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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DOID:7148 | rheumatoid arthritis | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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DOID:11335 | sarcoidosis | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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DOID:12361 | Graves' disease | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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DOID:399 | tuberculosis | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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DOID:8577 | ulcerative colitis | MGI:1859549 | Mus musculus (house mouse) | 547431 | Btnl2 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024