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:1324 | lung cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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DOID:783 | end stage renal disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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DOID:5844 | myocardial infarction | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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DOID:8719 | in situ carcinoma | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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DOID:6432 | pulmonary hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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DOID:3307 | teratoma | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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DOID:631 | fibromyalgia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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DOID:1586 | rheumatic fever | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:684 | hepatocellular carcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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DOID:5844 | myocardial infarction | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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DOID:784 | chronic kidney disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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DOID:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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DOID:12549 | hepatitis A | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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DOID:631 | fibromyalgia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:10591 | pre-eclampsia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:6713 | cerebrovascular disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:0110267 | cataract 44 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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DOID:9352 | type 2 diabetes mellitus | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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DOID:5419 | schizophrenia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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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