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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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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:0070040 | autosomal dominant intellectual developmental disorder 10 | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
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| DOID:0090080 | hypogonadotropic hypogonadism 16 with or without anosmia | HGNC:10723 | Homo sapiens (human) | 10371 | SEMA3A |
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| DOID:0050453 | lissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0112232 | lissencephaly 3 | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0112234 | microlissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0080918 | polymicrogyria | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0081017 | congenital fibrosis of the extraocular muscles 3A | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0060260 | ptosis | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:13934 | facial paralysis | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0090137 | complex cortical dysplasia with other brain malformations 1 | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0080143 | congenital fibrosis of the extraocular muscles | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0112227 | tubulinopathy | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0060798 | hypomyelinating leukodystrophy 6 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:13934 | facial paralysis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:3213 | demyelinating disease | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0060260 | ptosis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0090041 | torsion dystonia 4 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0112227 | tubulinopathy | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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