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:224 | transient cerebral ischemia | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
|
||
| DOID:13603 | obstructive jaundice | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
|
||
| DOID:0050770 | polycystic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
|
||
| DOID:12858 | Huntington's disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
|
||
| DOID:0070474 | childhood-onset neurodegeneration with brain atrophy | HGNC:12511 | Homo sapiens (human) | 7343 | UBTF |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:12510 | Homo sapiens (human) | 50613 | UBQLN3 |
|
||
| DOID:0060206 | amyotrophic lateral sclerosis type 15 | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
|
||
| DOID:9255 | frontotemporal dementia | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
|
||
| DOID:1289 | neurodegenerative disease | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
|
||
| DOID:1289 | neurodegenerative disease | HGNC:12508 | Homo sapiens (human) | 29979 | UBQLN1 |
|
||
| DOID:9255 | frontotemporal dementia | HGNC:12508 | Homo sapiens (human) | 29979 | UBQLN1 |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:12508 | Homo sapiens (human) | 29979 | UBQLN1 |
|
||
| DOID:0060206 | amyotrophic lateral sclerosis type 15 | HGNC:12508 | Homo sapiens (human) | 29979 | UBQLN1 |
|
||
| DOID:162 | cancer | HGNC:12502 | Homo sapiens (human) | 7341 | SUMO1 |
|
||
| DOID:0080403 | orofacial cleft 10 | HGNC:12502 | Homo sapiens (human) | 7341 | SUMO1 |
|
||
| DOID:10283 | prostate cancer | HGNC:125 | Homo sapiens (human) | 55 | ACP3 |
|
||
| DOID:0060393 | chromosome 15q11.2 deletion syndrome | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:1826 | epilepsy | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:0060041 | autism spectrum disorder | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:1059 | intellectual disability | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:1932 | Angelman syndrome | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
||
| DOID:4448 | macular degeneration | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
|
||
| DOID:8893 | psoriasis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
|
