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:2741 | bilirubin metabolic disorder | HGNC:10961 | Homo sapiens (human) | 28234 | SLCO1B3 |
|
||
| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
|
||
| DOID:0111407 | Fraser syndrome 2 | HGNC:25396 | Homo sapiens (human) | 341640 | FREM2 |
|
||
| DOID:0112034 | non-syndromic X-linked intellectual disability 9 | HGNC:13254 | Homo sapiens (human) | 24140 | FTSJ1 |
|
||
| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
|
||
| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
|
||
| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
|
||
| DOID:0081397 | Vissers-Bodmer syndrome | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
|
||
| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
|
||
| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
|
||
| DOID:0070538 | syndromic X-linked intellectual developmental disorder bain type | HGNC:5042 | Homo sapiens (human) | 3188 | HNRNPH2 |
|
||
| DOID:14768 | Saethre-Chotzen syndrome | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
|
||
| DOID:0111789 | Frank-Ter Haar syndrome | HGNC:29242 | Homo sapiens (human) | 285590 | SH3PXD2B |
|
||
| DOID:0050659 | biotin-responsive basal ganglia disease | HGNC:16266 | Homo sapiens (human) | 80704 | SLC19A3 |
|
||
| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
|
||
| DOID:0111464 | combined oxidative phosphorylation deficiency 35 | HGNC:20286 | Homo sapiens (human) | 54802 | TRIT1 |
|
||
| DOID:0060684 | autosomal dominant nocturnal frontal lobe epilepsy 3 | HGNC:1962 | Homo sapiens (human) | 1141 | CHRNB2 |
|
||
| DOID:0050547 | familial medullary thyroid carcinoma | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
|
||
| DOID:0081060 | X-linked nephrogenic diabetes insipidus | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
|
||
| DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
|
||
| DOID:0111459 | classic galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
|
||
| DOID:0110152 | Charcot-Marie-Tooth disease type 1B | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
|
||
| DOID:0050791 | persistent Mullerian duct syndrome | HGNC:465 | Homo sapiens (human) | 269 | AMHR2 |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
|
||
| DOID:0080209 | sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay | HGNC:17341 | Homo sapiens (human) | 51095 | TRNT1 |
|
