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:8778 | Crohn's disease | HGNC:3685 | Homo sapiens (human) | 2252 | FGF7 |
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DOID:8577 | ulcerative colitis | HGNC:3685 | Homo sapiens (human) | 2252 | FGF7 |
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DOID:10003 | sensorineural hearing loss | HGNC:2876 | Homo sapiens (human) | 1729 | DIAPH1 |
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DOID:10763 | hypertension | HGNC:9075 | Homo sapiens (human) | 5345 | SERPINF2 |
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DOID:9675 | pulmonary emphysema | MGI:1101771 | Mus musculus (house mouse) | 16591 | Kl |
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DOID:11054 | urinary bladder cancer | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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DOID:6419 | tetralogy of Fallot | MGI:103248 | Mus musculus (house mouse) | 13619 | Phc1 |
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DOID:2671 | transitional cell carcinoma | HGNC:11763 | Homo sapiens (human) | 7037 | TFRC |
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DOID:418 | systemic scleroderma | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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DOID:5082 | liver cirrhosis | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:2434 | Homo sapiens (human) | 1437 | CSF2 |
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DOID:3310 | atopic dermatitis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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DOID:0080199 | colorectal carcinoma | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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DOID:10652 | Alzheimer's disease | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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DOID:0081267 | graft-versus-host disease | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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DOID:8432 | polycythemia | RGD:3249 | Rattus norvegicus (Norway rat) | 24617 | Serpine1 |
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DOID:1612 | breast cancer | HGNC:6134 | Homo sapiens (human) | 3672 | ITGA1 |
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DOID:2581 | chondrodysplasia punctata | HGNC:719 | Homo sapiens (human) | 415 | ARSL |
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DOID:0060903 | thrombosis | HGNC:5181 | Homo sapiens (human) | 3273 | HRG |
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DOID:0111151 | Prinzmetal angina | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:3525 | middle cerebral artery infarction | RGD:3704 | Rattus norvegicus (Norway rat) | 24778 | Slc2a1 |
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DOID:898 | autosomal dominant polycystic kidney disease | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:12554 | hemolytic-uremic syndrome | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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DOID:13359 | Ehlers-Danlos syndrome | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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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