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:1612 | breast cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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DOID:162 | cancer | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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DOID:5419 | schizophrenia | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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DOID:1574 | alcohol use disorder | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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DOID:0060180 | colitis | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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DOID:3070 | high grade glioma | HGNC:10860 | Homo sapiens (human) | 6480 | ST6GAL1 |
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DOID:1574 | alcohol use disorder | HGNC:10860 | Homo sapiens (human) | 6480 | ST6GAL1 |
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DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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DOID:9975 | cocaine dependence | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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DOID:3669 | intermittent claudication | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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DOID:3070 | high grade glioma | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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DOID:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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DOID:3211 | lysosomal storage disease | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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DOID:3659 | sialuria | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:1094 | Homo sapiens (human) | 670 | BPHL |
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DOID:5742 | pancreatic acinar cell adenocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:1793 | pancreatic cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:1909 | melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:3070 | high grade glioma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:9256 | colorectal cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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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