Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
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 | July 29, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
|
||
| DOID:0080037 | Worth syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
|
||
| DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
|
||
| DOID:0080016 | spina bifida | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
|
||
| DOID:0080005 | bone remodeling disease | SGD:S000004954 | Saccharomyces cerevisiae S288C | 855723 | IDP3 |
|
||
| DOID:0080005 | bone remodeling disease | SGD:S000004164 | Saccharomyces cerevisiae S288C | 850871 | IDP2 |
|
||
| DOID:0080005 | bone remodeling disease | RGD:1597139 | Rattus norvegicus (Norway rat) | 361596 | Idh2 |
|
||
| DOID:0080005 | bone remodeling disease | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
|
||
| DOID:0080005 | bone remodeling disease | MGI:96414 | Mus musculus (house mouse) | 269951 | Idh2 |
|
||
| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
|
||
| DOID:0080000 | muscular disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
|
||
| DOID:0080000 | muscular disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
|
||
| DOID:0080000 | muscular disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
|
||
| DOID:0080000 | muscular disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
|
||
| DOID:0080000 | muscular disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
|
||
| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
|
||
| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | Acox1 |
|
||
| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | Xenbase:XB-GENE-984155 | Xenopus laevis (African clawed frog) | 447370 | ogdhl.L |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | MGI:1098267 | Mus musculus (house mouse) | 18293 | Ogdh |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | RGD:1561359 | Rattus norvegicus (Norway rat) | 360975 | Ogdh |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
|
