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:1184 | nephrotic syndrome | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:10652 | Alzheimer's disease | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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DOID:13141 | uveitis | RGD:621237 | Rattus norvegicus (Norway rat) | 25625 | Tnfrsf1a |
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DOID:0080311 | X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance | HGNC:8148 | Homo sapiens (human) | 4983 | OPHN1 |
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DOID:4481 | allergic rhinitis | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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DOID:9884 | muscular dystrophy | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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DOID:0111128 | focal segmental glomerulosclerosis 1 | MGI:1890773 | Mus musculus (house mouse) | 60595 | Actn4 |
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DOID:0110832 | Usher syndrome type 1F | MGI:1891428 | Mus musculus (house mouse) | 11994 | Pcdh15 |
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DOID:13628 | favism | MGI:105979 | Mus musculus (house mouse) | 14381 | G6pdx |
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DOID:12365 | malaria | MGI:96392 | Mus musculus (house mouse) | 15894 | Icam1 |
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DOID:9253 | gastrointestinal stromal tumor | MGI:96677 | Mus musculus (house mouse) | 16590 | Kit |
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DOID:3911 | progeria | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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DOID:4154 | dentinogenesis imperfecta | MGI:109172 | Mus musculus (house mouse) | 666279 | Dspp |
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DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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DOID:4450 | renal cell carcinoma | RGD:620349 | Rattus norvegicus (Norway rat) | 29527 | Ptgs2 |
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DOID:3911 | progeria | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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DOID:3827 | congenital diaphragmatic hernia | MGI:1315202 | Mus musculus (house mouse) | 20564 | Slit3 |
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DOID:13580 | cholestasis | RGD:2366 | Rattus norvegicus (Norway rat) | 25303 | Abcc2 |
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DOID:783 | end stage renal disease | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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DOID:1073 | renal hypertension | HGNC:7940 | Homo sapiens (human) | 4879 | NPPB |
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DOID:1073 | renal hypertension | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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DOID:0111103 | maturity-onset diabetes of the young type 4 | MGI:102851 | Mus musculus (house mouse) | 18609 | Pdx1 |
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DOID:8717 | decubitus ulcer | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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DOID:0060591 | WHIM syndrome | HGNC:2561 | Homo sapiens (human) | 7852 | CXCR4 |
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DOID:1826 | epilepsy | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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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