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:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
|
||
| DOID:0112227 | tubulinopathy | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
|
||
| DOID:13934 | facial paralysis | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
|
||
| DOID:0112240 | Leber congenital amaurosis with early-onset deafness | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
|
||
| DOID:0060798 | hypomyelinating leukodystrophy 6 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:13934 | facial paralysis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:3213 | demyelinating disease | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0060260 | ptosis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0090041 | torsion dystonia 4 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0112227 | tubulinopathy | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:14452 | hypokalemic periodic paralysis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0081017 | congenital fibrosis of the extraocular muscles 3A | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0060260 | ptosis | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:13934 | facial paralysis | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0090137 | complex cortical dysplasia with other brain malformations 1 | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0080143 | congenital fibrosis of the extraocular muscles | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0112227 | tubulinopathy | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
|
||
| DOID:0050453 | lissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
|
||
| DOID:0112232 | lissencephaly 3 | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
|
||
| DOID:0112234 | microlissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
|
||
| DOID:0080918 | polymicrogyria | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
|
