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 |
---|---|
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 |
---|---|---|---|---|---|---|---|---|
DOID:11476 | osteoporosis | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:12678 | hypercalcemia | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:0111341 | primary failure of tooth eruption | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:0111732 | Eiken syndrome | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:2256 | osteochondrodysplasia | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:3454 | brain infarction | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:0080020 | Jansen's metaphyseal chondrodysplasia | WB:WBGene00015735 | Caenorhabditis elegans | 175942 | pdfr-1 |
|
||
DOID:1459 | hypothyroidism | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
|
||
DOID:0111042 | glycogen storage disease IXa | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
|
||
DOID:0050545 | visceral heterotaxy | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
|
||
DOID:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
|
||
DOID:2747 | glycogen storage disease | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
|
||
DOID:0060256 | Dowling-Degos disease | WB:WBGene00015793 | Caenorhabditis elegans | 180607 | pfut-1 |
|
||
DOID:0050667 | alcohol-related neurodevelopmental disorder | WB:WBGene00015800 | Caenorhabditis elegans | 182643 | C15H9.4 |
|
||
DOID:12554 | hemolytic-uremic syndrome | WB:WBGene00015861 | Caenorhabditis elegans | 182687 | C16D9.6 |
|
||
DOID:0080520 | Tn polyagglutination syndrome | WB:WBGene00015861 | Caenorhabditis elegans | 182687 | C16D9.6 |
|
||
DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | WB:WBGene00015865 | Caenorhabditis elegans | 182693 | C16E9.1 |
|
||
DOID:0070221 | progressive familial intrahepatic cholestasis | WB:WBGene00015942 | Caenorhabditis elegans | 173966 | osta-2 |
|
||
DOID:0060419 | chromosome 3q29 microdeletion syndrome | WB:WBGene00015942 | Caenorhabditis elegans | 173966 | osta-2 |
|
||
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
|
||
DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | WB:WBGene00015982 | Caenorhabditis elegans | 182795 | bgnt-1.4 |
|
||
DOID:3908 | lung non-small cell carcinoma | WB:WBGene00016061 | Caenorhabditis elegans | 178934 | hpo-15 |
|
||
DOID:0070029 | ITM2B-related cerebral amyloid angiopathy 1 | WB:WBGene00016106 | Caenorhabditis elegans | 180816 | itm-2 |
|
||
DOID:0070030 | ITM2B-related cerebral amyloid angiopathy 2 | WB:WBGene00016106 | Caenorhabditis elegans | 180816 | itm-2 |
|
||
DOID:9246 | cerebral amyloid angiopathy | WB:WBGene00016106 | Caenorhabditis elegans | 180816 | itm-2 |
|
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