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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:0060807 | syndromic X-linked intellectual disability Najm type | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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| DOID:0060807 | syndromic X-linked intellectual disability Najm type | MGI:1355272 | Mus musculus (house mouse) | 104318 | Csnk1d |
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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:0060826 | syndromic X-linked intellectual disability Shashi type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:0060826 | syndromic X-linked intellectual disability Shashi type | MGI:1343044 | Mus musculus (house mouse) | 19655 | Rbmx |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | HGNC:20672 | Homo sapiens (human) | 23133 | PHF8 |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | MGI:2444341 | Mus musculus (house mouse) | 320595 | Phf8 |
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| DOID:0060802 | syndromic X-linked intellectual disability Snyder type | MGI:109490 | Mus musculus (house mouse) | 20603 | Sms |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | MGI:1926884 | Mus musculus (house mouse) | 59026 | Huwe1 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | RGD:69231 | Rattus norvegicus (Norway rat) | 63864 | Hsd17b10 |
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| DOID:0080985 | syndromic X-linked intellectual disorder Lujan-Fryns-type | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:0080985 | syndromic X-linked intellectual disorder Lujan-Fryns-type | SGD:S000000677 | Saccharomyces cerevisiae S288C | 850442 | SRB8 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | MGI:2661175 | Mus musculus (house mouse) | 245684 | Cnksr2 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | HGNC:19701 | Homo sapiens (human) | 22866 | CNKSR2 |
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| DOID:0050888 | syndromic intellectual disability | FB:FBgn0260938 | Drosophila melanogaster (fruit fly) | 32547 | tay |
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| DOID:0050888 | syndromic intellectual disability | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:0050888 | syndromic intellectual disability | MGI:106247 | Mus musculus (house mouse) | 28000 | Prpf19 |
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| DOID:0050888 | syndromic intellectual disability | HGNC:8148 | Homo sapiens (human) | 4983 | OPHN1 |
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| DOID:0050888 | syndromic intellectual disability | HGNC:19966 | Homo sapiens (human) | 57578 | UNC79 |
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