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:10283 | prostate cancer | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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DOID:0060180 | colitis | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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DOID:219 | colon cancer | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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DOID:0060647 | fetal encasement syndrome | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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DOID:5419 | schizophrenia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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DOID:10763 | hypertension | HGNC:17423 | Homo sapiens (human) | 55501 | CHST12 |
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DOID:3635 | congenital myasthenic syndrome | HGNC:1967 | Homo sapiens (human) | 1146 | CHRNG |
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DOID:1574 | alcohol use disorder | HGNC:1967 | Homo sapiens (human) | 1146 | CHRNG |
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DOID:0080110 | contractures, pterygia, and spondylocarpotarsal fusion syndrome | HGNC:1967 | Homo sapiens (human) | 1146 | CHRNG |
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DOID:3635 | congenital myasthenic syndrome | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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DOID:1574 | alcohol use disorder | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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DOID:0110679 | congenital myasthenic syndrome 4C | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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DOID:0110678 | congenital myasthenic syndrome 4A | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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DOID:0110677 | congenital myasthenic syndrome 4B | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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DOID:0110665 | congenital myasthenic syndrome 3B | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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DOID:1574 | alcohol use disorder | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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DOID:3635 | congenital myasthenic syndrome | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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DOID:0110666 | congenital myasthenic syndrome 3A | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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DOID:0110664 | congenital myasthenic syndrome 3C | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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DOID:1324 | lung cancer | HGNC:1964 | Homo sapiens (human) | 1143 | CHRNB4 |
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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