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:0080686 | tubular aggregate myopathy 2 | MGI:1925542 | Mus musculus (house mouse) | 109305 | Orai1 |
|
||
| DOID:12930 | dilated cardiomyopathy | MGI:1925542 | Mus musculus (house mouse) | 109305 | Orai1 |
|
||
| DOID:11984 | hypertrophic cardiomyopathy | MGI:1925542 | Mus musculus (house mouse) | 109305 | Orai1 |
|
||
| DOID:0050873 | follicular lymphoma | MGI:1924461 | Mus musculus (house mouse) | 109222 | Rarres1 |
|
||
| DOID:1909 | melanoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:3910 | lung adenocarcinoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:0060352 | Kleefstra syndrome 1 | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:986 | alopecia areata | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:3748 | esophagus squamous cell carcinoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:934 | viral infectious disease | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
|
||
| DOID:0070154 | hereditary sensory neuropathy type 1F | MGI:1924270 | Mus musculus (house mouse) | 109168 | Atl3 |
|
||
| DOID:0110791 | hereditary spastic paraplegia 3A | MGI:1924270 | Mus musculus (house mouse) | 109168 | Atl3 |
|
||
| DOID:2476 | hereditary spastic paraplegia | MGI:1924270 | Mus musculus (house mouse) | 109168 | Atl3 |
|
||
| DOID:0110147 | Bartter disease type 5 | HGNC:16353 | Homo sapiens (human) | 10916 | MAGED2 |
|
||
| DOID:0050834 | CHARGE syndrome | MGI:1924001 | Mus musculus (house mouse) | 109151 | Chd9 |
|
||
| DOID:0060041 | autism spectrum disorder | MGI:1924001 | Mus musculus (house mouse) | 109151 | Chd9 |
|
||
| DOID:1682 | congenital heart disease | MGI:1924001 | Mus musculus (house mouse) | 109151 | Chd9 |
|
||
| DOID:14793 | hypohidrotic ectodermal dysplasia | HGNC:2895 | Homo sapiens (human) | 10913 | EDAR |
|
||
| DOID:0111663 | ectodermal dysplasia 10A | HGNC:2895 | Homo sapiens (human) | 10913 | EDAR |
|
||
| DOID:0111665 | ectodermal dysplasia 10B | HGNC:2895 | Homo sapiens (human) | 10913 | EDAR |
|
||
| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
|
||
| DOID:1432 | blindness | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
|
||
| DOID:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
|
