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:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
|
||
| DOID:9269 | maple syrup urine disease | HGNC:2698 | Homo sapiens (human) | 1629 | DBT |
|
||
| DOID:13133 | HELLP syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
|
||
| DOID:3883 | Lynch syndrome | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
|
||
| DOID:0110863 | congenital stationary night blindness autosomal dominant 2 | HGNC:8786 | Homo sapiens (human) | 5158 | PDE6B |
|
||
| DOID:0110995 | Joubert syndrome 26 | HGNC:29068 | Homo sapiens (human) | 23247 | KATNIP |
|
||
| DOID:0060764 | autosomal recessive Robinow syndrome | HGNC:10257 | Homo sapiens (human) | 4920 | ROR2 |
|
||
| DOID:0050834 | CHARGE syndrome | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
|
||
| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
|
||
| DOID:3650 | lactic acidosis | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
|
||
| DOID:0110448 | dilated cardiomyopathy 1HH | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
|
||
| DOID:0060196 | amyotrophic lateral sclerosis type 4 | HGNC:445 | Homo sapiens (human) | 23064 | SETX |
|
||
| DOID:11836 | clubfoot | HGNC:9004 | Homo sapiens (human) | 5307 | PITX1 |
|
||
| DOID:10763 | hypertension | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
|
||
| DOID:12120 | pulmonary alveolar proteinosis | HGNC:2435 | Homo sapiens (human) | 1438 | CSF2RA |
|
||
| DOID:0111044 | gray platelet syndrome | HGNC:31928 | Homo sapiens (human) | 23218 | NBEAL2 |
|
||
| DOID:0110871 | congenital stationary night blindness 2A | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
|
||
| DOID:0050755 | spinocerebellar ataxia with axonal neuropathy 2 | HGNC:445 | Homo sapiens (human) | 23064 | SETX |
|
||
| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
|
||
| DOID:3210 | Pelizaeus-Merzbacher disease | HGNC:9086 | Homo sapiens (human) | 5354 | PLP1 |
|
||
| DOID:0080053 | Albright's hereditary osteodystrophy | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
|
||
| DOID:14264 | benign neonatal seizures | HGNC:6297 | Homo sapiens (human) | 3786 | KCNQ3 |
|
||
| DOID:0070378 | developmental and epileptic encephalopathy 109 | HGNC:24824 | Homo sapiens (human) | 51343 | FZR1 |
|
||
| DOID:0080041 | hypochondroplasia | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
|
||
| DOID:12930 | dilated cardiomyopathy | HGNC:333 | Homo sapiens (human) | 183 | AGT |
|
