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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:0111094 | Fanconi anemia complementation group N | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:1793 | pancreatic cancer | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:0050671 | female breast cancer | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:0111641 | autosomal recessive nonsyndromic deafness 94 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:0111485 | combined oxidative phosphorylation deficiency 24 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:26223 | Homo sapiens (human) | 79736 | TEFM |
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| DOID:9675 | pulmonary emphysema | ZFIN:ZDB-GENE-031118-20 | Danio rerio (zebrafish) | 797512 | fut8a |
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| DOID:14735 | hereditary angioedema | ZFIN:ZDB-GENE-090312-176 | Danio rerio (zebrafish) | 797517 | si:dkey-121b10.7 |
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| DOID:1928 | Williams-Beuren syndrome | HGNC:4041 | Homo sapiens (human) | 7976 | FZD3 |
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| DOID:5419 | schizophrenia | HGNC:4041 | Homo sapiens (human) | 7976 | FZD3 |
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| DOID:0050778 | Meckel syndrome | HGNC:20652 | Homo sapiens (human) | 79770 | TXNDC15 |
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| DOID:9970 | obesity | HGNC:30939 | Homo sapiens (human) | 79776 | ZFHX4 |
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| DOID:0110573 | autosomal dominant nonsyndromic deafness 4A | HGNC:23212 | Homo sapiens (human) | 79784 | MYH14 |
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| DOID:10003 | sensorineural hearing loss | HGNC:23212 | Homo sapiens (human) | 79784 | MYH14 |
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| DOID:0081209 | autosomal recessive intellectual developmental disorder 45 | HGNC:16510 | Homo sapiens (human) | 79791 | FBXO31 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:8466 | retinal degeneration | HGNC:11761 | Homo sapiens (human) | 7980 | TFPI2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:11761 | Homo sapiens (human) | 7980 | TFPI2 |
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| DOID:0060227 | Adams-Oliver syndrome | ZFIN:ZDB-GENE-120813-8 | Danio rerio (zebrafish) | 798087 | eogt |
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| DOID:934 | viral infectious disease | HGNC:24650 | Homo sapiens (human) | 79813 | EHMT1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:24650 | Homo sapiens (human) | 79813 | EHMT1 |
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| DOID:0060352 | Kleefstra syndrome 1 | HGNC:24650 | Homo sapiens (human) | 79813 | EHMT1 |
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| DOID:0080597 | Kleefstra syndrome | HGNC:24650 | Homo sapiens (human) | 79813 | EHMT1 |
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