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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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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:0070400 | hypomyelinating leukodystrophy 19 | HGNC:29118 | Homo sapiens (human) | 9725 | TMEM63A |
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| DOID:2256 | osteochondrodysplasia | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0050671 | female breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:0070050 | neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language | HGNC:6996 | Homo sapiens (human) | 4208 | MEF2C |
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| DOID:9256 | colorectal cancer | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0081150 | common variable immunodeficiency 7 | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:1574 | alcohol use disorder | HGNC:5298 | Homo sapiens (human) | 9177 | HTR3B |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0070035 | autosomal dominant intellectual developmental disorder 5 | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:1470 | major depressive disorder | HGNC:5234 | Homo sapiens (human) | 3305 | HSPA1L |
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| DOID:0070411 | autosomal recessive spinocerebellar ataxia 30 | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:1612 | breast cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:1227 | neutropenia | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:783 | end stage renal disease | HGNC:6027 | Homo sapiens (human) | 3579 | CXCR2 |
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| DOID:0110241 | cataract 41 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0110751 | type 1 diabetes mellitus 12 | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0111296 | generalized epilepsy with febrile seizures plus 10 | HGNC:4845 | Homo sapiens (human) | 348980 | HCN1 |
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| DOID:0081113 | Baraitser-Winter syndrome 2 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:12119 | hemosiderosis | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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