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GlyTouCan
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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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:0112329 | pontocerebellar hypoplasia type 2F | HGNC:16791 | Homo sapiens (human) | 116461 | TSEN15 |
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| DOID:0111547 | retinal arterial tortuosity | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:794 | Homo sapiens (human) | 471 | ATIC |
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| DOID:0081145 | common variable immunodeficiency 2 | HGNC:18153 | Homo sapiens (human) | 23495 | TNFRSF13B |
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| DOID:4247 | coronary restenosis | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0111967 | immunodeficiency 54 | HGNC:6947 | Homo sapiens (human) | 4173 | MCM4 |
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| DOID:0112199 | spondyloepimetaphyseal dysplasia with joint laxity type 2 | HGNC:6391 | Homo sapiens (human) | 3835 | KIF22 |
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| DOID:9970 | obesity | HGNC:11047 | Homo sapiens (human) | 11254 | SLC6A14 |
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| DOID:6432 | pulmonary hypertension | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0050591 | tooth agenesis | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:8545 | malignant hyperthermia | HGNC:1405 | Homo sapiens (human) | 786 | CACNG1 |
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| DOID:0050604 | acrocapitofemoral dysplasia | HGNC:5956 | Homo sapiens (human) | 3549 | IHH |
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| DOID:0112187 | thyroid dyshormonogenesis 3 | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:14330 | Parkinson's disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:0040086 | Polyomavirus-associated nephropathy | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:15840 | Homo sapiens (human) | 9757 | KMT2B |
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| DOID:750 | peptic ulcer disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:31042 | Homo sapiens (human) | 80000 | GREB1L |
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| DOID:3211 | lysosomal storage disease | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:11981 | morbid obesity | HGNC:4479 | Homo sapiens (human) | 2847 | MCHR1 |
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| DOID:0080596 | hyper IgE recurrent infection syndrome 4 | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:9675 | pulmonary emphysema | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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