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:0050540 | Charcot-Marie-Tooth disease type 3 | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
|
||
| DOID:0080325 | tuberous sclerosis 2 | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
|
||
| DOID:0090059 | enhanced S-cone syndrome | HGNC:7974 | Homo sapiens (human) | 10002 | NR2E3 |
|
||
| DOID:12120 | pulmonary alveolar proteinosis | HGNC:33 | Homo sapiens (human) | 21 | ABCA3 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
|
||
| DOID:9269 | maple syrup urine disease | HGNC:987 | Homo sapiens (human) | 594 | BCKDHB |
|
||
| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
|
||
| DOID:2566 | corneal dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
|
||
| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
|
||
| DOID:3627 | aortic aneurysm | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
|
||
| DOID:0060852 | Pierson syndrome | HGNC:6487 | Homo sapiens (human) | 3913 | LAMB2 |
|
||
| DOID:2030 | anxiety disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
|
||
| DOID:8545 | malignant hyperthermia | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
|
||
| DOID:10487 | Hirschsprung's disease | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
|
||
| DOID:0050473 | Alstrom syndrome | HGNC:428 | Homo sapiens (human) | 7840 | ALMS1 |
|
||
| DOID:0050554 | X-linked sideroblastic anemia with ataxia | HGNC:48 | Homo sapiens (human) | 22 | ABCB7 |
|
||
| DOID:1588 | thrombocytopenia | HGNC:11795 | Homo sapiens (human) | 7066 | THPO |
|
||
| DOID:14330 | Parkinson's disease | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
|
||
| DOID:0110918 | hereditary spherocytosis type 3 | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
|
||
| DOID:0110495 | autosomal recessive nonsyndromic deafness 37 | HGNC:7605 | Homo sapiens (human) | 4646 | MYO6 |
|
||
| DOID:0060814 | Wilson-Turner syndrome | HGNC:25726 | Homo sapiens (human) | 81887 | LAS1L |
|
||
| DOID:10629 | microphthalmia | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
|
||
| DOID:0110218 | Brugada syndrome 1 | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
|
||
| DOID:3070 | high grade glioma | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
|
