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:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
|
||
| DOID:83 | cataract | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
|
||
| DOID:0070339 | cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | HGNC:15822 | Homo sapiens (human) | 55074 | OXR1 |
|
||
| DOID:0070299 | multiple epiphyseal dysplasia 5 | HGNC:6909 | Homo sapiens (human) | 4148 | MATN3 |
|
||
| DOID:0050989 | episodic ataxia type 1 | HGNC:6218 | Homo sapiens (human) | 3736 | KCNA1 |
|
||
| DOID:0050574 | L-2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
|
||
| DOID:1596 | depressive disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
|
||
| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | HGNC:2076 | Homo sapiens (human) | 1203 | CLN5 |
|
||
| DOID:1612 | breast cancer | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
|
||
| DOID:0110945 | autosomal recessive osteopetrosis 6 | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
|
||
| DOID:0111181 | familial hemiplegic migraine 1 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
|
||
| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
|
||
| DOID:0111223 | centronuclear myopathy 1 | HGNC:2974 | Homo sapiens (human) | 1785 | DNM2 |
|
||
| DOID:0111083 | Fanconi anemia complementation group D2 | HGNC:3585 | Homo sapiens (human) | 2177 | FANCD2 |
|
||
| DOID:0110154 | Charcot-Marie-Tooth disease type 2A1 | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
|
||
| DOID:0060609 | microcephalic osteodysplastic primordial dwarfism type II | HGNC:16068 | Homo sapiens (human) | 5116 | PCNT |
|
||
| DOID:0111155 | autosomal recessive spinocerebellar ataxia 21 | HGNC:14372 | Homo sapiens (human) | 57410 | SCYL1 |
|
||
| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
||
| DOID:9970 | obesity | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
|
||
| DOID:0080422 | Dravet syndrome | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
|
||
| DOID:0050328 | congenital hypothyroidism | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
|
||
| DOID:0111074 | progressive familial heart block type IA | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
|
||
| DOID:0111918 | spermatogenic failure 40 | HGNC:25325 | Homo sapiens (human) | 255101 | CFAP65 |
|
||
| DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
|
||
| DOID:3082 | interstitial lung disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
|
