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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:5419 | schizophrenia | HGNC:704 | Homo sapiens (human) | 10095 | ARPC1B |
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| DOID:4029 | gastritis | HGNC:704 | Homo sapiens (human) | 10095 | ARPC1B |
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| DOID:0050328 | congenital hypothyroidism | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:612 | primary immunodeficiency disease | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:1508 | candidiasis | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:17223 | Homo sapiens (human) | 10090 | UST |
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| DOID:0081074 | Teebi hypertelorism syndrome 2 | HGNC:1750 | Homo sapiens (human) | 1009 | CDH11 |
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| DOID:0080631 | Elsahy-Waters syndrome | HGNC:1750 | Homo sapiens (human) | 1009 | CDH11 |
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| DOID:10273 | heart conduction disease | HGNC:6282 | Homo sapiens (human) | 10089 | KCNK7 |
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| DOID:5082 | liver cirrhosis | HGNC:51504 | Homo sapiens (human) | 100861540 | CYP3A7-CYP3A51P |
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| DOID:0060179 | Renpenning syndrome | HGNC:9330 | Homo sapiens (human) | 10084 | PQBP1 |
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| DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:9683 | Homo sapiens (human) | 10076 | PTPRU |
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| DOID:2527 | nephrosis | HGNC:9683 | Homo sapiens (human) | 10076 | PTPRU |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:9452 | steatotic liver disease | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
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| DOID:0080000 | muscular disease | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
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| DOID:9970 | obesity | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
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| DOID:0060404 | chromosome 17q12 deletion syndrome | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
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| DOID:3565 | meningioma | MGI:1923724 | Mus musculus (house mouse) | 100689 | Spon2 |
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| DOID:3042 | allergic contact dermatitis | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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