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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:0050426 | Stevens-Johnson syndrome | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:4930 | nasal cavity adenocarcinoma | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:1936 | atherosclerosis | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:3429 | inclusion body myositis | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:4449 | macular retinal edema | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:10763 | hypertension | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:13641 | exfoliation syndrome | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:6432 | pulmonary hypertension | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:8947 | diabetic retinopathy | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:8893 | psoriasis | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:418 | systemic scleroderma | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:0080226 | autosomal dominant intellectual developmental disorder 56 | HGNC:2092 | Homo sapiens (human) | 1213 | CLTC |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:33939 | Homo sapiens (human) | 645104 | CLRN2 |
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| DOID:0110828 | Usher syndrome type 3 | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0050439 | Usher syndrome | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0110841 | Usher syndrome type 3A | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0110373 | retinitis pigmentosa 61 | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:13270 | erythropoietic protoporphyria | HGNC:2088 | Homo sapiens (human) | 10845 | CLPX |
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| DOID:0050921 | pharynx squamous cell carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:3910 | lung adenocarcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:684 | hepatocellular carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:9261 | nasopharynx carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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