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:2921 | glomerulonephritis | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:14330 | Parkinson's disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:1459 | hypothyroidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:11383 | cryptorchidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:893 | Wilson disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:10652 | Alzheimer's disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:438 | autoimmune disease of the nervous system | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:418 | systemic scleroderma | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:7998 | hyperthyroidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:0080379 | nephrotic syndrome type 2 | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:5844 | myocardial infarction | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:12217 | Lewy body dementia | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:3587 | pancreatic ductal carcinoma | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:2565 | macular corneal dystrophy | RGD:1561144 | Rattus norvegicus (Norway rat) | 307859 | Chst5 |
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DOID:3323 | Sandhoff disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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DOID:12377 | spinal muscular atrophy | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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DOID:3211 | lysosomal storage disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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DOID:3320 | Tay-Sachs disease | HGNC:4878 | Homo sapiens (human) | 3073 | HEXA |
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DOID:83 | cataract | RGD:1303198 | Rattus norvegicus (Norway rat) | 306860 | Gcnt2 |
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DOID:0110242 | cataract 13 with adult i phenotype | RGD:1303198 | Rattus norvegicus (Norway rat) | 306860 | Gcnt2 |
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DOID:10908 | hydrocephalus | RGD:1310810 | Rattus norvegicus (Norway rat) | 306549 | Pomk |
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DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | RGD:1310810 | Rattus norvegicus (Norway rat) | 306549 | Pomk |
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DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | RGD:1310810 | Rattus norvegicus (Norway rat) | 306549 | Pomk |
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DOID:10763 | hypertension | RGD:1308214 | Rattus norvegicus (Norway rat) | 304322 | Chst12 |
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DOID:162 | cancer | RGD:1307107 | Rattus norvegicus (Norway rat) | 303872 | Pigz |
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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