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:0060041 | autism spectrum disorder | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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DOID:3803 | Crigler-Najjar syndrome | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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DOID:3907 | lung squamous cell carcinoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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DOID:3827 | congenital diaphragmatic hernia | MGI:104719 | Mus musculus (house mouse) | 15531 | Ndst1 |
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DOID:1826 | epilepsy | MGI:3036255 | Mus musculus (house mouse) | 237500 | Tmtc3 |
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DOID:1612 | breast cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:0050861 | colorectal adenocarcinoma | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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DOID:0080488 | mucolipidosis | MGI:3643902 | Mus musculus (house mouse) | 432486 | Gnptab |
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DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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DOID:10487 | Hirschsprung's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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DOID:9744 | type 1 diabetes mellitus | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:2945 | severe acute respiratory syndrome | MGI:2135738 | Mus musculus (house mouse) | 80908 | Abo |
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DOID:10952 | nephritis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:850 | lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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DOID:5419 | schizophrenia | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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DOID:2527 | nephrosis | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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DOID:0060050 | autoimmune disease of blood | ZFIN:ZDB-GENE-060503-810 | Danio rerio (zebrafish) | 555344 | c1galt1a |
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DOID:206 | hereditary multiple exostoses | RGD:62065 | Rattus norvegicus (Norway rat) | 56819 | Extl3 |
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DOID:2841 | asthma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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DOID:784 | chronic kidney disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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DOID:3393 | coronary artery disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:9675 | pulmonary emphysema | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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DOID:9256 | colorectal cancer | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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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