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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:0112311 | male infertility due to acephalic spermatozoa | HGNC:29616 | Homo sapiens (human) | 116840 | CNTROB |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:18748 | Homo sapiens (human) | 129684 | CNTNAP5 |
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| DOID:0060041 | autism spectrum disorder | HGNC:18748 | Homo sapiens (human) | 129684 | CNTNAP5 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:18747 | Homo sapiens (human) | 85445 | CNTNAP4 |
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| DOID:0060041 | autism spectrum disorder | HGNC:18747 | Homo sapiens (human) | 85445 | CNTNAP4 |
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| DOID:0060041 | autism spectrum disorder | HGNC:32035 | Homo sapiens (human) | 728577 | CNTNAP3B |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:32035 | Homo sapiens (human) | 728577 | CNTNAP3B |
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| DOID:0060041 | autism spectrum disorder | HGNC:13834 | Homo sapiens (human) | 79937 | CNTNAP3 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:13834 | Homo sapiens (human) | 79937 | CNTNAP3 |
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| DOID:1470 | major depressive disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:11257 | social phobia | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060488 | Pitt-Hopkins syndrome | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:13365 | reading disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:5419 | schizophrenia | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:4189 | mutism | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:1059 | intellectual disability | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:12849 | autistic disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060244 | specific language impairment | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:11832 | visual epilepsy | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:4186 | articulation disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:8011 | Homo sapiens (human) | 8506 | CNTNAP1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:8011 | Homo sapiens (human) | 8506 | CNTNAP1 |
|
