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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:0110436 | dilated cardiomyopathy 1L | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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| DOID:11724 | limb-girdle muscular dystrophy | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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| DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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| DOID:0090034 | myoclonic dystonia 11 | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
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| DOID:10534 | stomach cancer | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
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| DOID:0110436 | dilated cardiomyopathy 1L | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:9884 | muscular dystrophy | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0050700 | cardiomyopathy | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:9884 | muscular dystrophy | HGNC:10806 | Homo sapiens (human) | 6443 | SGCB |
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| DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | HGNC:10806 | Homo sapiens (human) | 6443 | SGCB |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | HGNC:10805 | Homo sapiens (human) | 6442 | SGCA |
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| DOID:767 | muscular atrophy | HGNC:10805 | Homo sapiens (human) | 6442 | SGCA |
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| DOID:9884 | muscular dystrophy | HGNC:10805 | Homo sapiens (human) | 6442 | SGCA |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:2799 | bronchiolitis obliterans | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:3082 | interstitial lung disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:0060071 | pre-malignant neoplasm | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:11335 | sarcoidosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:0050127 | sinusitis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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