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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:2377 | multiple sclerosis | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:0050742 | nicotine dependence | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:1681 | heart septal defect | HGNC:14630 | Homo sapiens (human) | 78987 | CRELD1 |
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| DOID:0111298 | familial febrile seizures 8 | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:0080105 | microcephaly and chorioretinopathy 1 | HGNC:18127 | Homo sapiens (human) | 85378 | TUBGCP6 |
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| DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:3393 | coronary artery disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3883 | Lynch syndrome | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
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| DOID:0111458 | galactose epimerase deficiency | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:0050741 | alcohol dependence | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:9775 | diastolic heart failure | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:0080911 | cerebrooculofacioskeletal syndrome 1 | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:409 | liver disease | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:2841 | asthma | HGNC:263 | Homo sapiens (human) | 135 | ADORA2A |
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| DOID:0060752 | familial temporal lobe epilepsy 5 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:2843 | long QT syndrome | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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| DOID:0050144 | Kartagener syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0070340 | classic citrullinemia | HGNC:758 | Homo sapiens (human) | 445 | ASS1 |
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| DOID:3526 | cerebral infarction | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:0111380 | solitary median maxillary central incisor | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:9206 | Barrett's esophagus | HGNC:18831 | Homo sapiens (human) | 115908 | CTHRC1 |
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| DOID:5844 | myocardial infarction | HGNC:6293 | Homo sapiens (human) | 3783 | KCNN4 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:1324 | lung cancer | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
|
