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:9870 | galactosemia | MGI:95638 | Mus musculus (house mouse) | 14430 | Galt |
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DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | MGI:894695 | Mus musculus (house mouse) | 14425 | Galnt3 |
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DOID:0110645 | long QT syndrome 2 | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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DOID:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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DOID:4079 | heart valve disease | MGI:894693 | Mus musculus (house mouse) | 14423 | Galnt1 |
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DOID:0110777 | hereditary spastic paraplegia 26 | MGI:1342057 | Mus musculus (house mouse) | 14421 | B4galnt1 |
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DOID:13276 | Mycoplasma pneumoniae pneumonia | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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DOID:11949 | Creutzfeldt-Jakob disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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DOID:10587 | Krabbe disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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DOID:1909 | melanoma | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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DOID:83 | cataract | HGNC:18301 | Homo sapiens (human) | 144195 | SLC2A14 |
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DOID:10763 | hypertension | HGNC:18301 | Homo sapiens (human) | 144195 | SLC2A14 |
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DOID:1826 | epilepsy | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:11832 | visual epilepsy | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:0060764 | autosomal recessive Robinow syndrome | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:0060041 | autism spectrum disorder | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:3328 | temporal lobe epilepsy | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:0111448 | progressive myoclonus epilepsy 1B | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:12583 | velocardiofacial syndrome | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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DOID:3312 | bipolar disorder | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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DOID:670 | amphetamine abuse | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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DOID:9351 | diabetes mellitus | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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DOID:0112223 | developmental and epileptic encephalopathy 89 | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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DOID:2030 | anxiety disorder | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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DOID:0050741 | alcohol dependence | MGI:95632 | Mus musculus (house mouse) | 14415 | Gad1 |
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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