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:1826 | epilepsy | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
|
||
| DOID:2355 | anemia | HGNC:13811 | Homo sapiens (human) | 57282 | SLC4A10 |
|
||
| DOID:0111474 | combined oxidative phosphorylation deficiency 1 | HGNC:13780 | Homo sapiens (human) | 85476 | GFM1 |
|
||
| DOID:0080036 | SOST-related sclerosing bone dysplasia | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
|
||
| DOID:0060251 | sclerosteosis | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
|
||
| DOID:0060756 | sclerosteosis 1 | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
|
||
| DOID:0080807 | autosomal dominant craniodiaphyseal dysplasia | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
|
||
| DOID:8893 | psoriasis | HGNC:13765 | Homo sapiens (human) | 64806 | IL25 |
|
||
| DOID:10808 | gastric ulcer | HGNC:13765 | Homo sapiens (human) | 64806 | IL25 |
|
||
| DOID:3310 | atopic dermatitis | HGNC:13765 | Homo sapiens (human) | 64806 | IL25 |
|
||
| DOID:0111722 | amelogenesis imperfecta type 3C | HGNC:13764 | Homo sapiens (human) | 84957 | RELT |
|
||
| DOID:0060393 | chromosome 15q11.2 deletion syndrome | HGNC:13760 | Homo sapiens (human) | 26999 | CYFIP2 |
|
||
| DOID:0080430 | developmental and epileptic encephalopathy 65 | HGNC:13760 | Homo sapiens (human) | 26999 | CYFIP2 |
|
||
| DOID:0111715 | Schaaf-Yang syndrome | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
|
||
| DOID:0060393 | chromosome 15q11.2 deletion syndrome | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
|
||
| DOID:3328 | temporal lobe epilepsy | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
|
||
| DOID:5419 | schizophrenia | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
|
||
| DOID:0060041 | autism spectrum disorder | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
|
||
| DOID:10584 | retinitis pigmentosa | HGNC:1375 | Homo sapiens (human) | 762 | CA4 |
|
||
| DOID:0050866 | oral squamous cell carcinoma | HGNC:13746 | Homo sapiens (human) | 57795 | BRINP2 |
|
||
| DOID:11723 | Duchenne muscular dystrophy | HGNC:13741 | Homo sapiens (human) | 54221 | SNTG2 |
|
||
| DOID:0112008 | pituitary adenoma 5 | HGNC:13733 | Homo sapiens (human) | 64072 | CDH23 |
|
||
| DOID:0110467 | autosomal recessive nonsyndromic deafness 12 | HGNC:13733 | Homo sapiens (human) | 64072 | CDH23 |
|
||
| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:13733 | Homo sapiens (human) | 64072 | CDH23 |
|
||
| DOID:0110831 | Usher syndrome type 1D | HGNC:13733 | Homo sapiens (human) | 64072 | CDH23 |
|
