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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:0111973 | immunodeficiency 17 | HGNC:1675 | Homo sapiens (human) | 917 | CD3G |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:4798 | Homo sapiens (human) | 3026 | HABP2 |
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| DOID:8632 | Kaposi's sarcoma | HGNC:3581 | Homo sapiens (human) | 2186 | BPTF |
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| DOID:1470 | major depressive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0111961 | immunodeficiency 26 | HGNC:9413 | Homo sapiens (human) | 5591 | PRKDC |
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| DOID:0070030 | ITM2B-related cerebral amyloid angiopathy 2 | HGNC:6174 | Homo sapiens (human) | 9445 | ITM2B |
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| DOID:0112024 | non-syndromic X-linked intellectual disability 58 | HGNC:11854 | Homo sapiens (human) | 7102 | TSPAN7 |
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| DOID:12849 | autistic disorder | HGNC:3287 | Homo sapiens (human) | 1977 | EIF4E |
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| DOID:0110458 | dilated cardiomyopathy 1BB | HGNC:3049 | Homo sapiens (human) | 1829 | DSG2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6026 | Homo sapiens (human) | 3577 | CXCR1 |
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| DOID:0110374 | retinitis pigmentosa 68 | HGNC:29326 | Homo sapiens (human) | 57709 | SLC7A14 |
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| DOID:0080526 | bronchiectasis 1 | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0080523 | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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| DOID:0081146 | common variable immunodeficiency 3 | HGNC:1633 | Homo sapiens (human) | 930 | CD19 |
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| DOID:0070130 | autosomal dominant cutis laxa 1 | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:0081177 | autosomal recessive intellectual developmental disorder 1 | HGNC:9477 | Homo sapiens (human) | 8492 | PRSS12 |
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| DOID:0111428 | essential tremor 1 | HGNC:3024 | Homo sapiens (human) | 1814 | DRD3 |
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| DOID:0111389 | mucopolysaccharidosis Ih/s | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:4531 | Homo sapiens (human) | 27199 | OXGR1 |
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| DOID:0060788 | hypomyelinating leukodystrophy 10 | HGNC:30262 | Homo sapiens (human) | 29920 | PYCR2 |
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| DOID:0081213 | autosomal recessive intellectual developmental disorder 50 | HGNC:26114 | Homo sapiens (human) | 80153 | EDC3 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:25604 | Homo sapiens (human) | 55262 | TRAPPC14 |
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| DOID:0090084 | hypogonadotropic hypogonadism 5 with or without anosmia | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:0110895 | inflammatory bowel disease 14 | HGNC:6120 | Homo sapiens (human) | 3663 | IRF5 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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