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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:0111635 | autosomal recessive nonsyndromic deafness 57 | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:0070473 | Zaki syndrome | HGNC:30238 | Homo sapiens (human) | 79971 | WLS |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:2799 | Homo sapiens (human) | 79977 | GRHL2 |
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| DOID:0110557 | autosomal dominant nonsyndromic deafness 28 | HGNC:2799 | Homo sapiens (human) | 79977 | GRHL2 |
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| DOID:0080669 | posterior polymorphous corneal dystrophy 4 | HGNC:2799 | Homo sapiens (human) | 79977 | GRHL2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:16165 | Homo sapiens (human) | 79980 | DSN1 |
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| DOID:9256 | colorectal cancer | HGNC:16165 | Homo sapiens (human) | 79980 | DSN1 |
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| DOID:2018 | hyperinsulinism | ZFIN:ZDB-GENE-060503-530 | Danio rerio (zebrafish) | 799867 | ptprfb |
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| DOID:9970 | obesity | ZFIN:ZDB-GENE-060503-530 | Danio rerio (zebrafish) | 799867 | ptprfb |
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| DOID:14227 | azoospermia | ZFIN:ZDB-GENE-060503-530 | Danio rerio (zebrafish) | 799867 | ptprfb |
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| DOID:0050589 | inflammatory bowel disease | ZFIN:ZDB-GENE-041014-161 | Danio rerio (zebrafish) | 799868 | st6galnac1.2 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:26292 | Homo sapiens (human) | 79993 | ELOVL7 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:1441 | Homo sapiens (human) | 800 | CALD1 |
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| DOID:14766 | renal agenesis | HGNC:31042 | Homo sapiens (human) | 80000 | GREB1L |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:31042 | Homo sapiens (human) | 80000 | GREB1L |
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| DOID:162 | cancer | HGNC:15682 | Homo sapiens (human) | 80012 | PHC3 |
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| DOID:3981 | pantothenate kinase-associated neurodegeneration | HGNC:15894 | Homo sapiens (human) | 80025 | PANK2 |
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| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
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| DOID:83 | cataract | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
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| DOID:10629 | microphthalmia | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
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| DOID:0060246 | MASA syndrome | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
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| DOID:4621 | holoprosencephaly | HGNC:25712 | Homo sapiens (human) | 80055 | PGAP1 |
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| DOID:1059 | intellectual disability | HGNC:20397 | Homo sapiens (human) | 80063 | ATF7IP2 |
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