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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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 | October 9, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
|
||
| DOID:0060838 | isolated microphthalmia 7 | HGNC:4218 | Homo sapiens (human) | 9573 | GDF3 |
|
||
| DOID:0060838 | isolated microphthalmia 7 | Xenbase:XB-GENE-865693 | Xenopus laevis (African clawed frog) | 394305 | gdf3.S |
|
||
| DOID:0060838 | isolated microphthalmia 7 | ZFIN:ZDB-GENE-980526-389 | Danio rerio (zebrafish) | 30125 | gdf3 |
|
||
| DOID:0060838 | isolated microphthalmia 7 | Xenbase:XB-GENE-487309 | Xenopus tropicalis (tropical clawed frog) | 493288 | gdf3 |
|
||
| DOID:0060838 | isolated microphthalmia 7 | MGI:95686 | Mus musculus (house mouse) | 14562 | Gdf3 |
|
||
| DOID:0060837 | isolated microphthalmia 5 | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
|
||
| DOID:0060837 | isolated microphthalmia 5 | MGI:2385957 | Mus musculus (house mouse) | 259172 | Mfrp |
|
||
| DOID:0060836 | isolated microphthalmia 4 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
|
||
| DOID:0060836 | isolated microphthalmia 4 | RGD:620104 | Rattus norvegicus (Norway rat) | 252834 | Gdf6 |
|
||
| DOID:0060836 | isolated microphthalmia 4 | ZFIN:ZDB-GENE-980526-373 | Danio rerio (zebrafish) | 566470 | gdf6a |
|
||
| DOID:0060836 | isolated microphthalmia 4 | ZFIN:ZDB-GENE-980526-442 | Danio rerio (zebrafish) | 30180 | gdf6b |
|
||
| DOID:0060836 | isolated microphthalmia 4 | MGI:95689 | Mus musculus (house mouse) | 242316 | Gdf6 |
|
||
| DOID:0060835 | isolated microphthalmia 6 | HGNC:39433 | Homo sapiens (human) | 646960 | PRSS56 |
|
||
| DOID:0060835 | isolated microphthalmia 6 | MGI:1916703 | Mus musculus (house mouse) | 69453 | Prss56 |
|
||
| DOID:0060832 | Griscelli syndrome type 1 | HGNC:7602 | Homo sapiens (human) | 4644 | MYO5A |
|
||
| DOID:0060832 | Griscelli syndrome type 1 | RGD:3143 | Rattus norvegicus (Norway rat) | 25017 | Myo5a |
|
||
| DOID:0060832 | Griscelli syndrome type 1 | MGI:105976 | Mus musculus (house mouse) | 17918 | Myo5a |
|
||
| DOID:0060827 | X-linked intellectual disability-psychosis-macroorchidism syndrome | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
|
||
| DOID:0060827 | X-linked intellectual disability-psychosis-macroorchidism syndrome | RGD:3075 | Rattus norvegicus (Norway rat) | 29386 | Mecp2 |
|
||
| DOID:0060827 | X-linked intellectual disability-psychosis-macroorchidism syndrome | MGI:99918 | Mus musculus (house mouse) | 17257 | Mecp2 |
|
||
| DOID:0060826 | syndromic X-linked intellectual disability Shashi type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
|
||
| DOID:0060826 | syndromic X-linked intellectual disability Shashi type | MGI:1343044 | Mus musculus (house mouse) | 19655 | Rbmx |
|
||
| DOID:0060825 | Christianson syndrome | MGI:2443511 | Mus musculus (house mouse) | 236794 | Slc9a6 |
|
||
| DOID:0060825 | Christianson syndrome | HGNC:11079 | Homo sapiens (human) | 10479 | SLC9A6 |
|
