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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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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:3347 | osteosarcoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:14330 | Parkinson's disease | HGNC:11330 | Homo sapiens (human) | 6751 | SSTR1 |
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| DOID:14330 | Parkinson's disease | HGNC:11331 | Homo sapiens (human) | 6752 | SSTR2 |
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| DOID:14330 | Parkinson's disease | HGNC:11332 | Homo sapiens (human) | 6753 | SSTR3 |
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| DOID:14330 | Parkinson's disease | HGNC:11333 | Homo sapiens (human) | 6754 | SSTR4 |
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| DOID:1824 | status epilepticus | HGNC:11333 | Homo sapiens (human) | 6754 | SSTR4 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | MGI:1914792 | Mus musculus (house mouse) | 67542 | Cog6 |
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| DOID:0060480 | left ventricular noncompaction | MGI:1914797 | Mus musculus (house mouse) | 67547 | Slc39a8 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | MGI:1914797 | Mus musculus (house mouse) | 67547 | Slc39a8 |
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| DOID:0060250 | idiopathic scoliosis | MGI:1914797 | Mus musculus (house mouse) | 67547 | Slc39a8 |
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| DOID:14330 | Parkinson's disease | HGNC:11334 | Homo sapiens (human) | 6755 | SSTR5 |
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| DOID:3312 | bipolar disorder | HGNC:11334 | Homo sapiens (human) | 6755 | SSTR5 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | MGI:1914824 | Mus musculus (house mouse) | 67574 | Alg13 |
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| DOID:0060374 | orofaciodigital syndrome IV | MGI:1914840 | Mus musculus (house mouse) | 67590 | Tctn3 |
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| DOID:0110987 | Joubert syndrome 18 | MGI:1914840 | Mus musculus (house mouse) | 67590 | Tctn3 |
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| DOID:0080443 | developmental and epileptic encephalopathy 21 | MGI:1914852 | Mus musculus (house mouse) | 67602 | Necap1 |
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| DOID:2999 | granulosa cell tumor | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:4450 | renal cell carcinoma | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:0060720 | autosomal recessive congenital ichthyosis 11 | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:12894 | Sjogren's syndrome | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:4441 | dysgerminoma | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:557 | kidney disease | MGI:1914953 | Mus musculus (house mouse) | 67703 | Kirrel3 |
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| DOID:1184 | nephrotic syndrome | MGI:1914953 | Mus musculus (house mouse) | 67703 | Kirrel3 |
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