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:0060668 | anencephaly | WB:WBGene00001165 | Caenorhabditis elegans | 176882 | efn-4 |
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DOID:13580 | cholestasis | WB:WBGene00012364 | Caenorhabditis elegans | 179991 | zmp-4 |
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DOID:10914 | amnestic disorder | WB:WBGene00000035 | Caenorhabditis elegans | 181706 | ace-1 |
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DOID:0110639 | congenital muscular dystrophy due to integrin alpha-7 deficiency | WB:WBGene00002081 | Caenorhabditis elegans | 176296 | ina-1 |
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DOID:9182 | pemphigus | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:62 | aortic valve disease | WB:WBGene00002299 | Caenorhabditis elegans | 174462 | let-23 |
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DOID:11832 | visual epilepsy | WB:WBGene00002299 | Caenorhabditis elegans | 174462 | let-23 |
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DOID:1657 | ventricular septal defect | WB:WBGene00012364 | Caenorhabditis elegans | 179991 | zmp-4 |
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DOID:8893 | psoriasis | WB:WBGene00006894 | Caenorhabditis elegans | 175182 | ver-1 |
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DOID:11832 | visual epilepsy | WB:WBGene00000083 | Caenorhabditis elegans | 181022 | adt-2 |
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DOID:5453 | pulmonary venoocclusive disease | WB:WBGene00006318 | Caenorhabditis elegans | 173613 | sup-9 |
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DOID:13948 | bladder neck obstruction | WB:WBGene00008890 | Caenorhabditis elegans | 184572 | ser-5 |
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DOID:438 | autoimmune disease of the nervous system | WB:WBGene00011474 | Caenorhabditis elegans | 176788 | aldo-1 |
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DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | WB:WBGene00008918 | Caenorhabditis elegans | 179519 | pigt-1 |
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DOID:589 | congenital hemolytic anemia | WB:WBGene00019844 | Caenorhabditis elegans | 180943 | abts-4 |
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DOID:234 | colon adenocarcinoma | WB:WBGene00019624 | Caenorhabditis elegans | 190096 | rnst-2 |
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DOID:14502 | cholesterol ester storage disease | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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DOID:5241 | hemangioblastoma | WB:WBGene00004963 | Caenorhabditis elegans | 173042 | spe-9 |
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DOID:0050848 | obstructive sleep apnea | WB:WBGene00003995 | Caenorhabditis elegans | 178215 | pgp-1 |
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DOID:12930 | dilated cardiomyopathy | WB:WBGene00017557 | Caenorhabditis elegans | 173685 | nep-11 |
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DOID:1074 | kidney failure | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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DOID:2917 | cryoglobulinemia | WB:WBGene00003995 | Caenorhabditis elegans | 178215 | pgp-1 |
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DOID:1498 | cholera | WB:WBGene00000253 | Caenorhabditis elegans | 171608 | bli-3 |
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DOID:1070 | primary open angle glaucoma | WB:WBGene00004860 | Caenorhabditis elegans | 174044 | sma-6 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | WB:WBGene00004804 | Caenorhabditis elegans | 177343 | skn-1 |
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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