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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:0081217 | autosomal recessive intellectual developmental disorder 56 | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:11476 | osteoporosis | HGNC:1440 | Homo sapiens (human) | 799 | CALCR |
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| DOID:10283 | prostate cancer | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:104 | bacterial infectious disease | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:3192 | neurilemmoma | HGNC:25752 | Homo sapiens (human) | 79915 | ATAD5 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:26293 | Homo sapiens (human) | 79925 | SPEF2 |
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| DOID:0111917 | spermatogenic failure 43 | HGNC:26293 | Homo sapiens (human) | 79925 | SPEF2 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:24583 | Homo sapiens (human) | 79930 | DOK3 |
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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:0070062 | Arboleda-Tham syndrome | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:11198 | DiGeorge syndrome | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:9119 | acute myeloid leukemia | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:0050574 | L-2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0080201 | Peters plus syndrome | ZFIN:ZDB-GENE-110411-147 | Danio rerio (zebrafish) | 799443 | b3glcta |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110838 | Usher syndrome type 2A | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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