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:0060307 | autosomal dominant intellectual developmental disorder | HGNC:22474 | Homo sapiens (human) | 9969 | MED13 |
|
||
| DOID:9970 | obesity | HGNC:22474 | Homo sapiens (human) | 9969 | MED13 |
|
||
| DOID:14227 | azoospermia | HGNC:1734 | Homo sapiens (human) | 997 | CDC34 |
|
||
| DOID:1682 | congenital heart disease | HGNC:1734 | Homo sapiens (human) | 997 | CDC34 |
|
||
| DOID:5679 | retinal disease | MGI:2139793 | Mus musculus (house mouse) | 99712 | Cept1 |
|
||
| DOID:1824 | status epilepticus | MGI:96670 | Mus musculus (house mouse) | 99738 | Kcnc4 |
|
||
| DOID:10652 | Alzheimer's disease | MGI:96670 | Mus musculus (house mouse) | 99738 | Kcnc4 |
|
||
| DOID:11446 | sciatic neuropathy | MGI:96670 | Mus musculus (house mouse) | 99738 | Kcnc4 |
|
||
| DOID:0050651 | atrioventricular septal defect | HGNC:7963 | Homo sapiens (human) | 9975 | NR1D2 |
|
||
| DOID:3328 | temporal lobe epilepsy | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:4971 | myelofibrosis | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:4483 | rhinitis | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:557 | kidney disease | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:3355 | fibrosarcoma | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:674 | cleft palate | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:225 | syndrome | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:1793 | pancreatic cancer | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:0060775 | microvillus inclusion disease | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:0060669 | cerebral cavernous malformation | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:3312 | bipolar disorder | HGNC:1736 | Homo sapiens (human) | 998 | CDC42 |
|
||
| DOID:14250 | Down syndrome | HGNC:1291 | Homo sapiens (human) | 9980 | DOP1B |
|
||
| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:19070 | Homo sapiens (human) | 9984 | THOC1 |
|
||
| DOID:2841 | asthma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
|
||
| DOID:10283 | prostate cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
|
