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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
LM-GlycoRepo
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:0111481 | combined oxidative phosphorylation deficiency 11 | HGNC:21176 | Homo sapiens (human) | 55005 | RMND1 |
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| DOID:0060230 | basal ganglia calcification | HGNC:14686 | Homo sapiens (human) | 58494 | JAM2 |
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| DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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| DOID:0080979 | arthrogryposis multiplex congenita-3 | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:0112025 | female-restricted syndromic X-linked intellectual disability 99 | HGNC:12632 | Homo sapiens (human) | 8239 | USP9X |
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| DOID:0080871 | primary ovarian insufficiency 14 | HGNC:4224 | Homo sapiens (human) | 2661 | GDF9 |
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| DOID:0080540 | galactosialidosis | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:0060587 | Noonan syndrome 9 | HGNC:11188 | Homo sapiens (human) | 6655 | SOS2 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:0110027 | age related macular degeneration 15 | HGNC:1358 | Homo sapiens (human) | 735 | C9 |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:0070509 | Schinzel Giedion syndrome | HGNC:15573 | Homo sapiens (human) | 26040 | SETBP1 |
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| DOID:0080786 | Brown-Vialetto-Van Laere syndrome 2 | HGNC:30224 | Homo sapiens (human) | 79581 | SLC52A2 |
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| DOID:0112236 | lissencephaly 6 | HGNC:6217 | Homo sapiens (human) | 10300 | KATNB1 |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0081209 | autosomal recessive intellectual developmental disorder 45 | HGNC:16510 | Homo sapiens (human) | 79791 | FBXO31 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0080776 | partial androgen insensitivity syndrome | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:0110543 | autosomal dominant nonsyndromic deafness 11 | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | POPDC1 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0111944 | immunodeficiency 31B | HGNC:11362 | Homo sapiens (human) | 6772 | STAT1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:564 | Homo sapiens (human) | 1173 | AP2M1 |
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| DOID:10605 | short bowel syndrome | HGNC:24039 | Homo sapiens (human) | 79827 | CLMP |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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