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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
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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:0111870 | nonphotosensitive trichothiodystrophy 7 | HGNC:11572 | Homo sapiens (human) | 6897 | TARS1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:0112274 | X-linked spermatogenic failure 3 | HGNC:26708 | Homo sapiens (human) | 286464 | CFAP47 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:0050449 | pachyonychia congenita | HGNC:6427 | Homo sapiens (human) | 3872 | KRT17 |
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| DOID:0081371 | lacrimoauriculodentodigital syndrome 2 | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0060259 | renal-hepatic-pancreatic dysplasia | HGNC:7907 | Homo sapiens (human) | 27031 | NPHP3 |
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| DOID:0112210 | developmental and epileptic encephalopathy 74 | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:0080493 | ovarian dysgenesis 1 | HGNC:3969 | Homo sapiens (human) | 2492 | FSHR |
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| DOID:0080581 | hyperekplexia 4 | HGNC:25903 | Homo sapiens (human) | 84896 | ATAD1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:15632 | Homo sapiens (human) | 51311 | TLR8 |
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| DOID:0080107 | microcephaly and chorioretinopathy 3 | HGNC:16691 | Homo sapiens (human) | 27229 | TUBGCP4 |
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| DOID:0111332 | Pitt-Hopkins-like syndrome 2 | HGNC:8008 | Homo sapiens (human) | 9378 | NRXN1 |
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| DOID:0112147 | retinitis pigmentosa 90 | HGNC:5384 | Homo sapiens (human) | 3419 | IDH3A |
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| DOID:0090011 | immunodeficiency-centromeric instability-facial anomalies syndrome 4 | HGNC:4861 | Homo sapiens (human) | 3070 | HELLS |
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| DOID:0070292 | primary autosomal recessive microcephaly 9 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
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| DOID:0081360 | spastic quadriplegic cerebral palsy 2 | HGNC:19309 | Homo sapiens (human) | 23189 | KANK1 |
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| DOID:0081372 | lacrimoauriculodentodigital syndrome 3 | HGNC:3666 | Homo sapiens (human) | 2255 | FGF10 |
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| DOID:0111607 | distal arthrogryposis type 3 | HGNC:26270 | Homo sapiens (human) | 63895 | PIEZO2 |
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| DOID:0110202 | Charcot-Marie-Tooth disease dominant intermediate A | HGNC:4181 | Homo sapiens (human) | 8729 | GBF1 |
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| DOID:1700 | X-linked ichthyosis | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:0070249 | autosomal dominant Emery-Dreifuss muscular dystrophy 4 | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:0081017 | congenital fibrosis of the extraocular muscles 3A | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0110082 | arrhythmogenic right ventricular dysplasia 11 | HGNC:3036 | Homo sapiens (human) | 1824 | DSC2 |
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