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:0050589 | inflammatory bowel disease | HGNC:437 | Homo sapiens (human) | 248 | ALPI |
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DOID:1024 | leprosy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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DOID:10283 | prostate cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:0110645 | long QT syndrome 2 | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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DOID:3393 | coronary artery disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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DOID:9970 | obesity | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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DOID:0111460 | cardiofaciocutaneous syndrome 1 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0014667 | disease of metabolism | HGNC:932 | Homo sapiens (human) | 570 | BAAT |
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DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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DOID:12732 | intermediate uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:10591 | pre-eclampsia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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DOID:11650 | bronchopulmonary dysplasia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:3907 | lung squamous cell carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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DOID:417 | autoimmune disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:10763 | hypertension | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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DOID:12129 | bulimia nervosa | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:4249 | Gerstmann-Straussler-Scheinker syndrome | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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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