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:326 | ischemia | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:2526 | prostate adenocarcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:3070 | high grade glioma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:10286 | prostate carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:162 | cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:10283 | prostate cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:9993 | hypoglycemia | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:11612 | polycystic ovary syndrome | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:14330 | Parkinson's disease | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:10763 | hypertension | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:1380 | endometrial cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:9256 | colorectal cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:4001 | ovarian carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:684 | hepatocellular carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:3069 | malignant astrocytoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:1574 | alcohol use disorder | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:9970 | obesity | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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DOID:5212 | congenital disorder of glycosylation | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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DOID:0080563 | congenital disorder of glycosylation Ik | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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DOID:5212 | congenital disorder of glycosylation | MGI:1098592 | Mus musculus (house mouse) | 208624 | Alg3 |
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DOID:0080556 | congenital disorder of glycosylation Id | MGI:1098592 | Mus musculus (house mouse) | 208624 | Alg3 |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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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