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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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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:0111485 | combined oxidative phosphorylation deficiency 24 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:2228 | thrombocytosis | HGNC:11795 | Homo sapiens (human) | 7066 | THPO |
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| DOID:9974 | drug dependence | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:3310 | atopic dermatitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:0050741 | alcohol dependence | HGNC:6232 | Homo sapiens (human) | 9312 | KCNB2 |
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| DOID:12783 | migraine without aura | HGNC:6547 | Homo sapiens (human) | 3949 | LDLR |
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| DOID:0060882 | renal hypomagnesemia 4 | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:0081110 | keratosis palmoplantaris striata 3 | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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| DOID:2841 | asthma | HGNC:2766 | Homo sapiens (human) | 1672 | DEFB1 |
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| DOID:5419 | schizophrenia | HGNC:8031 | Homo sapiens (human) | 4914 | NTRK1 |
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| DOID:10754 | otitis media | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2219 | Homo sapiens (human) | 1299 | COL9A3 |
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| DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:23212 | Homo sapiens (human) | 79784 | MYH14 |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:15754 | Homo sapiens (human) | 10398 | MYL9 |
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| DOID:0111799 | syndromic microphthalmia 1 | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:684 | hepatocellular carcinoma | RGD:621871 | Rattus norvegicus (Norway rat) | 26195 | Mt-co1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:1040 | chronic lymphocytic leukemia | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:0111707 | Bothnian type palmoplantar keratoderma | HGNC:638 | Homo sapiens (human) | 362 | AQP5 |
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