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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:0080487 | peroxisome biogenesis disorder 13A | HGNC:8856 | Homo sapiens (human) | 5195 | PEX14 |
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| DOID:0080156 | X-linked adrenal hypoplasia congenita | HGNC:7960 | Homo sapiens (human) | 190 | NR0B1 |
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| DOID:0080505 | Cornelia de Lange syndrome 1 | HGNC:28862 | Homo sapiens (human) | 25836 | NIPBL |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:0110786 | hereditary spastic paraplegia 35 | HGNC:21197 | Homo sapiens (human) | 79152 | FA2H |
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| DOID:0070037 | autosomal dominant intellectual developmental disorder 7 | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:0110739 | neurodegeneration with brain iron accumulation 5 | HGNC:28912 | Homo sapiens (human) | 11152 | WDR45 |
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| DOID:0110079 | Leber congenital amaurosis 8 | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:4249 | Gerstmann-Straussler-Scheinker syndrome | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:9256 | colorectal cancer | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:9821 | choroideremia | HGNC:1940 | Homo sapiens (human) | 1121 | CHM |
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| DOID:0111922 | spermatogenic failure 31 | HGNC:17728 | Homo sapiens (human) | 83449 | PMFBP1 |
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| DOID:0111030 | hemochromatosis type 3 | HGNC:11762 | Homo sapiens (human) | 7036 | TFR2 |
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| DOID:0111675 | neurooculocardiogenitourinary syndrome | HGNC:31406 | Homo sapiens (human) | 22884 | WDR37 |
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| DOID:0080054 | achondrogenesis type IA | HGNC:12305 | Homo sapiens (human) | 9321 | TRIP11 |
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| DOID:0081430 | intellectual developmental disorder with autistic features and language delay, with or without seizures | HGNC:30212 | Homo sapiens (human) | 26115 | TANC2 |
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| DOID:0110034 | X-linked Alport syndrome | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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| DOID:0070351 | spinal muscular atrophy with lower extremity predominant 1 | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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| DOID:0060690 | autosomal dominant auditory neuropathy 1 | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:5724 | Homo sapiens (human) | 3516 | RBPJ |
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| DOID:0110862 | congenital stationary night blindness autosomal dominant 1 | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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| DOID:0050683 | Bothnia retinal dystrophy | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | HGNC:11049 | Homo sapiens (human) | 6531 | SLC6A3 |
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| DOID:0081168 | HMG-CoA synthase 2 deficiency | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
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