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:0112313 | brain small vessel disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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DOID:526 | human immunodeficiency virus infectious disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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DOID:6000 | congestive heart failure | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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DOID:5844 | myocardial infarction | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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DOID:9970 | obesity | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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DOID:2754 | glycogen storage disease VI | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
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DOID:2747 | glycogen storage disease | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
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DOID:3650 | lactic acidosis | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
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DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:0060250 | idiopathic scoliosis | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:557 | kidney disease | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:0080322 | polycystic kidney disease | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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DOID:2738 | pseudoxanthoma elasticum | RGD:620093 | Rattus norvegicus (Norway rat) | 64133 | Xylt1 |
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DOID:557 | kidney disease | RGD:620093 | Rattus norvegicus (Norway rat) | 64133 | Xylt1 |
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DOID:9744 | type 1 diabetes mellitus | RGD:620093 | Rattus norvegicus (Norway rat) | 64133 | Xylt1 |
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DOID:0060462 | Desbuquois dysplasia | RGD:620093 | Rattus norvegicus (Norway rat) | 64133 | Xylt1 |
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DOID:0080322 | polycystic kidney disease | RGD:619765 | Rattus norvegicus (Norway rat) | 64134 | Xylt2 |
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DOID:2738 | pseudoxanthoma elasticum | RGD:619765 | Rattus norvegicus (Norway rat) | 64134 | Xylt2 |
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DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | ZFIN:ZDB-GENE-051120-24 | Danio rerio (zebrafish) | 641495 | poglut1 |
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DOID:0060256 | Dowling-Degos disease | ZFIN:ZDB-GENE-051120-24 | Danio rerio (zebrafish) | 641495 | poglut1 |
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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