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:813 | septic arthritis | MGI:88335 | Mus musculus (house mouse) | 12504 | Cd4 |
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DOID:635 | acquired immunodeficiency syndrome | MGI:88335 | Mus musculus (house mouse) | 12504 | Cd4 |
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DOID:0112277 | immunodeficiency 79 | MGI:88335 | Mus musculus (house mouse) | 12504 | Cd4 |
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DOID:0080600 | COVID-19 | MGI:88335 | Mus musculus (house mouse) | 12504 | Cd4 |
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DOID:0111973 | immunodeficiency 17 | MGI:88333 | Mus musculus (house mouse) | 12502 | Cd3g |
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DOID:627 | severe combined immunodeficiency | MGI:88331 | Mus musculus (house mouse) | 12500 | Cd3d |
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DOID:0111972 | immunodeficiency 19 | MGI:88331 | Mus musculus (house mouse) | 12500 | Cd3d |
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DOID:0050741 | alcohol dependence | HGNC:250 | Homo sapiens (human) | 125 | ADH1B |
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DOID:1927 | sphingolipidosis | HGNC:26992 | Homo sapiens (human) | 124976 | SPNS2 |
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DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:26992 | Homo sapiens (human) | 124976 | SPNS2 |
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DOID:0111643 | autosomal recessive nonsyndromic deafness 115 | HGNC:26992 | Homo sapiens (human) | 124976 | SPNS2 |
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DOID:12236 | primary biliary cholangitis | MGI:1096863 | Mus musculus (house mouse) | 12496 | Entpd2 |
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DOID:10763 | hypertension | MGI:1096863 | Mus musculus (house mouse) | 12496 | Entpd2 |
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DOID:5082 | liver cirrhosis | MGI:1096863 | Mus musculus (house mouse) | 12496 | Entpd2 |
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DOID:3070 | high grade glioma | MGI:1096863 | Mus musculus (house mouse) | 12496 | Entpd2 |
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DOID:1459 | hypothyroidism | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:0110815 | hereditary spastic paraplegia 64 | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:3213 | demyelinating disease | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:224 | transient cerebral ischemia | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:1852 | intrahepatic cholestasis | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:10591 | pre-eclampsia | MGI:102805 | Mus musculus (house mouse) | 12495 | Entpd1 |
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DOID:9744 | type 1 diabetes mellitus | MGI:107474 | Mus musculus (house mouse) | 12494 | Cd38 |
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DOID:9352 | type 2 diabetes mellitus | MGI:107474 | Mus musculus (house mouse) | 12494 | Cd38 |
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DOID:891 | progressive myoclonus epilepsy | MGI:1196458 | Mus musculus (house mouse) | 12492 | Scarb2 |
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DOID:0111444 | progressive myoclonus epilepsy 4 | MGI:1196458 | Mus musculus (house mouse) | 12492 | Scarb2 |
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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