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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
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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:9261 | nasopharynx carcinoma | HGNC:7381 | Homo sapiens (human) | 4486 | MST1R |
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| DOID:0111153 | congenital mirror movement disorder | HGNC:2701 | Homo sapiens (human) | 1630 | DCC |
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| DOID:0110482 | autosomal recessive nonsyndromic deafness 24 | HGNC:9944 | Homo sapiens (human) | 5962 | RDX |
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| DOID:612 | primary immunodeficiency disease | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:0070467 | carpal tunnel syndrome 2 | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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| DOID:0111212 | autosomal dominant distal hereditary motor neuronopathy 9 | HGNC:12729 | Homo sapiens (human) | 7453 | WARS1 |
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| DOID:0081182 | autosomal recessive intellectual developmental disorder 6 | HGNC:4580 | Homo sapiens (human) | 2898 | GRIK2 |
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| DOID:0111359 | large congenital melanocytic nevus | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0110398 | retinitis pigmentosa 51 | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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| DOID:0111745 | cerebellar ataxia type 43 | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:0112029 | non-syndromic X-linked intellectual disability 50 | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0111943 | immunodeficiency 48 | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:12869 | Homo sapiens (human) | 7543 | ZFX |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | HGNC:11529 | Homo sapiens (human) | 4072 | EPCAM |
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| DOID:0081148 | common variable immunodeficiency 5 | HGNC:7315 | Homo sapiens (human) | 931 | MS4A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8805 | Homo sapiens (human) | 5157 | PDGFRL |
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| DOID:13543 | hyperparathyroidism | HGNC:14006 | Homo sapiens (human) | 55503 | TRPV6 |
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| DOID:0110265 | cataract 31 multiple types | HGNC:16171 | Homo sapiens (human) | 128866 | CHMP4B |
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| DOID:6364 | migraine | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0111994 | immunodeficiency 45 | HGNC:5433 | Homo sapiens (human) | 3455 | IFNAR2 |
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| DOID:0081124 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 | HGNC:18188 | Homo sapiens (human) | 54499 | TMCO1 |
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| DOID:1171 | hyperlipoproteinemia type V | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:10584 | retinitis pigmentosa | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:0070028 | APP-related cerebral amyloid angiopathy | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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