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:1459 | hypothyroidism | RGD:631339 | Rattus norvegicus (Norway rat) | 288583 | Plod3 |
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DOID:7941 | Barrett's adenocarcinoma | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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DOID:9206 | Barrett's esophagus | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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DOID:1793 | pancreatic cancer | RGD:1306727 | Rattus norvegicus (Norway rat) | 288161 | B3galt5 |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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DOID:0060256 | Dowling-Degos disease | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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DOID:0080556 | congenital disorder of glycosylation Id | RGD:1306004 | Rattus norvegicus (Norway rat) | 287983 | Alg3 |
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DOID:5212 | congenital disorder of glycosylation | RGD:1306004 | Rattus norvegicus (Norway rat) | 287983 | Alg3 |
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DOID:0050589 | inflammatory bowel disease | RGD:1562048 | Rattus norvegicus (Norway rat) | 287920 | St6galnac1 |
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DOID:13129 | severe pre-eclampsia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:11996 | spermatic cord torsion | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:9408 | acute myocardial infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:0050731 | vitamin B12 deficiency | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:10763 | hypertension | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:4948 | gallbladder carcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:7941 | Barrett's adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:224 | transient cerebral ischemia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:1596 | depressive disorder | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:0080199 | colorectal carcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:1324 | lung cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:10591 | pre-eclampsia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:0080797 | nasal type extranodal NK/T-cell lymphoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:1184 | nephrotic syndrome | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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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