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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:0050454 | periventricular nodular heterotopia | HGNC:6836 | Homo sapiens (human) | 4131 | MAP1B |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:22474 | Homo sapiens (human) | 9969 | MED13 |
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| DOID:0110976 | brachydactyly type E2 | HGNC:9607 | Homo sapiens (human) | 5744 | PTHLH |
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| DOID:0080990 | King Denborough syndrome | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
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| DOID:3526 | cerebral infarction | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:9970 | obesity | HGNC:10660 | Homo sapiens (human) | 9672 | SDC3 |
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| DOID:0080499 | ovarian dysgenesis 7 | HGNC:14508 | Homo sapiens (human) | 56945 | MRPS22 |
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| DOID:0070521 | peeling skin syndrome 2 | HGNC:11781 | Homo sapiens (human) | 9333 | TGM5 |
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| DOID:0060790 | hypomyelinating leukodystrophy 3 | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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| DOID:8567 | Hodgkin's lymphoma | HGNC:28557 | Homo sapiens (human) | 200942 | KLHDC8B |
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| DOID:0110222 | Brugada syndrome 5 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6637 | Homo sapiens (human) | 4001 | LMNB1 |
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| DOID:9256 | colorectal cancer | HGNC:9645 | Homo sapiens (human) | 5782 | PTPN12 |
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| DOID:0111726 | geleophysic dysplasia 2 | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:0112167 | autosomal dominant nonsyndromic deafness 76 | HGNC:9090 | Homo sapiens (human) | 5357 | PLS1 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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| DOID:0080722 | Kenny-Caffey syndrome type 1 | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:0081231 | autosomal recessive intellectual developmental disorder 70 | HGNC:24152 | Homo sapiens (human) | 51319 | RSRC1 |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:6055 | Homo sapiens (human) | 3617 | IMPG1 |
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| DOID:0111278 | histiocytosis-lymphadenopathy plus syndrome | HGNC:23096 | Homo sapiens (human) | 55315 | SLC29A3 |
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| DOID:0111643 | autosomal recessive nonsyndromic deafness 115 | HGNC:26992 | Homo sapiens (human) | 124976 | SPNS2 |
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| DOID:0081218 | autosomal recessive intellectual developmental disorder 74 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0112297 | spondylometaphyseal dysplasia corner fracture type | HGNC:3778 | Homo sapiens (human) | 2335 | FN1 |
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