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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
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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:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | RGD:1309526 | Rattus norvegicus (Norway rat) | 366478 | Pigv |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | MGI:2442480 | Mus musculus (house mouse) | 230801 | Pigv |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | RGD:727962 | Rattus norvegicus (Norway rat) | 378774 | Pigw |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | MGI:1917575 | Mus musculus (house mouse) | 70325 | Pigw |
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| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
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| DOID:0070425 | combined oxidative phosphorylation deficiency 52 | HGNC:15910 | Homo sapiens (human) | 9054 | NFS1 |
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| DOID:0070423 | early onset progressive encephalopathy with brain atrophy and thin corpus callosum | HGNC:11581 | Homo sapiens (human) | 6904 | TBCD |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | HGNC:4327 | Homo sapiens (human) | 2742 | GLRA2 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | MGI:95748 | Mus musculus (house mouse) | 237213 | Glra2 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | WB:WBGene00001591 | Caenorhabditis elegans | 180086 | glc-1 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | RGD:2705 | Rattus norvegicus (Norway rat) | 24397 | Glra2 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | WB:WBGene00001592 | Caenorhabditis elegans | 172103 | glc-2 |
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| DOID:0070420 | developmental delay, hypotonia, and impaired language | HGNC:16712 | Homo sapiens (human) | 55294 | FBXW7 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | RGD:3115 | Rattus norvegicus (Norway rat) | 29152 | Mstn |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | MGI:1338027 | Mus musculus (house mouse) | 14561 | Gdf11 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | WB:WBGene00000903 | Caenorhabditis elegans | 175237 | daf-7 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | ZFIN:ZDB-GENE-990415-165 | Danio rerio (zebrafish) | 798441 | mstnb |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | HGNC:4216 | Homo sapiens (human) | 10220 | GDF11 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | HGNC:4223 | Homo sapiens (human) | 2660 | MSTN |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | RGD:2673 | Rattus norvegicus (Norway rat) | 29454 | Gdf11 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | MGI:95691 | Mus musculus (house mouse) | 17700 | Mstn |
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| DOID:0070417 | neurodevelopmental disorder with speech impairment and dysmorphic facies | HGNC:29010 | Homo sapiens (human) | 9739 | SETD1A |
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| DOID:0070417 | neurodevelopmental disorder with speech impairment and dysmorphic facies | MGI:2652820 | Mus musculus (house mouse) | 208043 | Setd1b |
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