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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:784 | chronic kidney disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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| DOID:0060748 | familial temporal lobe epilepsy 1 | HGNC:6572 | Homo sapiens (human) | 9211 | LGI1 |
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| DOID:83 | cataract | HGNC:6610 | Homo sapiens (human) | 3982 | LIM2 |
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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:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:8947 | diabetic retinopathy | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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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:0110923 | familial hemophagocytic lymphohistiocytosis 3 | HGNC:23147 | Homo sapiens (human) | 201294 | UNC13D |
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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:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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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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| DOID:0070202 | familial partial lipodystrophy type 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110678 | congenital myasthenic syndrome 4A | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:0060825 | Christianson syndrome | HGNC:11079 | Homo sapiens (human) | 10479 | SLC9A6 |
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