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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:12849 | autistic disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0111275 | speech-language disorder-1 | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:93 | language disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:5419 | schizophrenia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:4428 | dyslexia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0110551 | autosomal dominant nonsyndromic deafness 21 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:0110465 | autosomal recessive nonsyndromic deafness 104 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:11830 | myopia | HGNC:13869 | Homo sapiens (human) | 84695 | LOXL3 |
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| DOID:1184 | nephrotic syndrome | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
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| DOID:680 | tauopathy | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
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| DOID:0111999 | immunodeficiency 61 | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:5041 | esophageal cancer | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:3459 | breast carcinoma | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:1749 | squamous cell carcinoma | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:13841 | Homo sapiens (human) | 57211 | ADGRG6 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:13841 | Homo sapiens (human) | 57211 | ADGRG6 |
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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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