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:90 | degenerative disc disease | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:4480 | achondroplasia | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:6000 | congestive heart failure | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:7148 | rheumatoid arthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
|
||
| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
|
||
| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
|
||
| DOID:1574 | alcohol use disorder | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
|
||
| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
|
||
| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
|
||
| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
|
||
| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:21497 | Homo sapiens (human) | 28976 | ACAD9 |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0080000 | muscular disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:9452 | steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:9970 | obesity | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
|
