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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:0110927 | nemaline myopathy 3 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0070166 | spermatogenic failure 20 | HGNC:25631 | Homo sapiens (human) | 55779 | CFAP44 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:0110017 | age related macular degeneration 4 | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0060866 | patterned macular dystrophy 1 | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0110390 | retinitis pigmentosa 1 | HGNC:10263 | Homo sapiens (human) | 6101 | RP1 |
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| DOID:0110636 | congenital merosin-deficient muscular dystrophy 1A | HGNC:6482 | Homo sapiens (human) | 3908 | LAMA2 |
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| DOID:8398 | osteoarthritis | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080442 | developmental and epileptic encephalopathy 41 | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:0110596 | primary ciliary dyskinesia 21 | HGNC:24245 | Homo sapiens (human) | 92749 | DRC1 |
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| DOID:0080570 | congenital disorder of glycosylation It | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080021 | Schmid metaphyseal chondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:0081364 | neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:2436 | Homo sapiens (human) | 1439 | CSF2RB |
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| DOID:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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