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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:1059 | intellectual disability | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
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| DOID:11335 | sarcoidosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18410 | Homo sapiens (human) | 23036 | ZNF292 |
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| DOID:0110501 | autosomal recessive nonsyndromic deafness 44 | HGNC:232 | Homo sapiens (human) | 107 | ADCY1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9642 | Homo sapiens (human) | 5770 | PTPN1 |
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| DOID:10325 | silicosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:6307 | Homo sapiens (human) | 3791 | KDR |
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| DOID:0060240 | UV-sensitive syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0111468 | combined oxidative phosphorylation deficiency 25 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0110757 | type 1 diabetes mellitus 20 | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:2559 | opiate dependence | HGNC:24154 | Homo sapiens (human) | 168667 | BMPER |
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| DOID:0111363 | Heinz body anemia | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:0060706 | X-linked lymphoproliferative syndrome 2 | HGNC:592 | Homo sapiens (human) | 331 | XIAP |
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| DOID:9849 | Meniere's disease | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:7147 | ankylosing spondylitis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:0110548 | autosomal dominant nonsyndromic deafness 17 | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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| DOID:4467 | clear cell renal cell carcinoma | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:3687 | MELAS syndrome | HGNC:7461 | Homo sapiens (human) | 4540 | ND5 |
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