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:12842 | Guillain-Barre syndrome | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:0050523 | adult T-cell leukemia/lymphoma | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:418 | systemic scleroderma | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:9538 | multiple myeloma | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:2518 | orchitis | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:12449 | aplastic anemia | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:2917 | cryoglobulinemia | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:11123 | Henoch-Schoenlein purpura | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:1040 | chronic lymphocytic leukemia | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:2799 | bronchiolitis obliterans | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:10124 | corneal disease | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:9952 | acute lymphoblastic leukemia | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:2957 | pulmonary tuberculosis | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:9119 | acute myeloid leukemia | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:3525 | middle cerebral artery infarction | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:2841 | asthma | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:6432 | pulmonary hypertension | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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DOID:5844 | myocardial infarction | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:10591 | pre-eclampsia | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:783 | end stage renal disease | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:11400 | pyelonephritis | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:9074 | systemic lupus erythematosus | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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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