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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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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:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | HGNC:2974 | Homo sapiens (human) | 1785 | DNM2 |
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| DOID:856 | biotinidase deficiency | HGNC:1122 | Homo sapiens (human) | 686 | BTD |
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| DOID:0080062 | autosomal recessive spinocerebellar ataxia 13 | HGNC:4593 | Homo sapiens (human) | 2911 | GRM1 |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0112135 | severe congenital neutropenia 8 | HGNC:11301 | Homo sapiens (human) | 6729 | SRP54 |
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| DOID:0090004 | progressive pseudorheumatoid arthropathy of childhood | HGNC:12771 | Homo sapiens (human) | 8838 | CCN6 |
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| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0080235 | autosomal dominant intellectual developmental disorder 48 | HGNC:9801 | Homo sapiens (human) | 5879 | RAC1 |
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| DOID:0080042 | autosomal recessive spinocerebellar ataxia 18 | HGNC:4576 | Homo sapiens (human) | 2895 | GRID2 |
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| DOID:0060748 | familial temporal lobe epilepsy 1 | HGNC:6572 | Homo sapiens (human) | 9211 | LGI1 |
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| DOID:0110346 | osteogenesis imperfecta type 10 | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:0110977 | brachydactyly type A1C | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110144 | Bartter disease type 3 | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0050632 | oculocutaneous albinism | HGNC:2709 | Homo sapiens (human) | 1638 | DCT |
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| DOID:0070537 | spastic tetraplegia, thin corpus callosum, and progressive microcephaly | HGNC:10942 | Homo sapiens (human) | 6509 | SLC1A4 |
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| DOID:0060287 | cornea plana | HGNC:6309 | Homo sapiens (human) | 11081 | KERA |
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| DOID:0110679 | congenital myasthenic syndrome 4C | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:3347 | osteosarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0060546 | Hermansky-Pudlak syndrome 8 | HGNC:20914 | Homo sapiens (human) | 388552 | BLOC1S3 |
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| DOID:0110199 | Charcot-Marie-Tooth disease dominant intermediate C | HGNC:12840 | Homo sapiens (human) | 8565 | YARS1 |
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| DOID:0110915 | childhood hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | HGNC:4216 | Homo sapiens (human) | 10220 | GDF11 |
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| DOID:0110612 | primary ciliary dyskinesia 10 | HGNC:20188 | Homo sapiens (human) | 55172 | DNAAF2 |
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