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 | July 29, 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:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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DOID:12351 | alcoholic hepatitis | RGD:3369 | Rattus norvegicus (Norway rat) | 25747 | Ppara |
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DOID:6000 | congestive heart failure | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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DOID:5844 | myocardial infarction | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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DOID:0080554 | congenital disorder of glycosylation Ib | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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DOID:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
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DOID:206 | hereditary multiple exostoses | Xenbase:XB-GENE-867525 | Xenopus tropicalis (tropical clawed frog) | 448393 | ext1 |
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DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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DOID:9352 | type 2 diabetes mellitus | RGD:68396 | Rattus norvegicus (Norway rat) | 65038 | Inppl1 |
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DOID:5212 | congenital disorder of glycosylation | Xenbase:XB-GENE-6485822 | Xenopus laevis (African clawed frog) | 108706812 | b4galt1.1.S |
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DOID:0060222 | Scheie syndrome | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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DOID:4195 | hyperglycemia | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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DOID:10223 | dermatomyositis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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DOID:14330 | Parkinson's disease | HGNC:8999 | Homo sapiens (human) | 23761 | PISD |
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DOID:12236 | primary biliary cholangitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:11446 | sciatic neuropathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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DOID:2300 | spondylolysis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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DOID:1459 | hypothyroidism | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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DOID:3371 | chondrosarcoma | FB:FBgn0064237 | Drosophila melanogaster (fruit fly) | 37104 | Idgf5 |
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DOID:2741 | bilirubin metabolic disorder | FB:FBgn0015663 | Drosophila melanogaster (fruit fly) | 44058 | Ugt36A1 |
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DOID:0014667 | disease of metabolism | MGI:96572 | Mus musculus (house mouse) | 16333 | Ins1 |
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DOID:4362 | cervical cancer | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:3908 | lung non-small cell carcinoma | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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DOID:9352 | type 2 diabetes mellitus | MGI:97370 | Mus musculus (house mouse) | 18605 | Enpp1 |
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DOID:418 | systemic scleroderma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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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 v4.0.0
Last updated: August 19, 2024