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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:0112104 | Sotos syndrome 3 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0080409 | familial adenomatous polyposis 1 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0081218 | autosomal recessive intellectual developmental disorder 74 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:9256 | colorectal cancer | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0070005 | Seckel syndrome 9 | HGNC:30764 | Homo sapiens (human) | 10293 | TRAIP |
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| DOID:0111222 | centronuclear myopathy 5 | HGNC:16901 | Homo sapiens (human) | 10290 | SPEG |
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| DOID:12858 | Huntington's disease | MGI:104807 | Mus musculus (house mouse) | 102866 | Pls3 |
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| DOID:11476 | osteoporosis | MGI:104807 | Mus musculus (house mouse) | 102866 | Pls3 |
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| DOID:3827 | congenital diaphragmatic hernia | MGI:104807 | Mus musculus (house mouse) | 102866 | Pls3 |
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| DOID:1612 | breast cancer | HGNC:975 | Homo sapiens (human) | 10286 | BCAS2 |
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| DOID:1824 | status epilepticus | MGI:2147834 | Mus musculus (house mouse) | 102857 | Slc6a8 |
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| DOID:0050800 | cerebral creatine deficiency syndrome 1 | MGI:2147834 | Mus musculus (house mouse) | 102857 | Slc6a8 |
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| DOID:1059 | intellectual disability | MGI:2147834 | Mus musculus (house mouse) | 102857 | Slc6a8 |
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| DOID:10584 | retinitis pigmentosa | HGNC:10664 | Homo sapiens (human) | 10283 | CWC27 |
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| DOID:0080238 | autosomal dominant intellectual developmental disorder 47 | HGNC:11354 | Homo sapiens (human) | 10274 | STAG1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:9119 | acute myeloid leukemia | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:1612 | breast cancer | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:2671 | transitional cell carcinoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:5409 | lung small cell carcinoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:5223 | infertility | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:11446 | sciatic neuropathy | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:2920 | membranoproliferative glomerulonephritis | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:8552 | chronic myeloid leukemia | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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