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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:0081354 | congenital myopathy 22A | MGI:98250 | Mus musculus (house mouse) | 110880 | Scn4a |
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| DOID:0081354 | congenital myopathy 22A | ZFIN:ZDB-GENE-051201-2 | Danio rerio (zebrafish) | 572442 | scn4aa |
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| DOID:0081354 | congenital myopathy 22A | FB:FBgn0285944 | Drosophila melanogaster (fruit fly) | 32619 | para |
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| DOID:0081354 | congenital myopathy 22A | ZFIN:ZDB-GENE-051201-1 | Danio rerio (zebrafish) | 564977 | scn4ab |
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| DOID:0081355 | congenital myopathy 22B | ZFIN:ZDB-GENE-051201-1 | Danio rerio (zebrafish) | 564977 | scn4ab |
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| DOID:0081355 | congenital myopathy 22B | ZFIN:ZDB-GENE-051201-2 | Danio rerio (zebrafish) | 572442 | scn4aa |
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| DOID:0081355 | congenital myopathy 22B | MGI:98250 | Mus musculus (house mouse) | 110880 | Scn4a |
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| DOID:0081355 | congenital myopathy 22B | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0081355 | congenital myopathy 22B | FB:FBgn0285944 | Drosophila melanogaster (fruit fly) | 32619 | para |
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| DOID:0081355 | congenital myopathy 22B | RGD:3636 | Rattus norvegicus (Norway rat) | 25722 | Scn4a |
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| DOID:0081356 | spinal muscular atrophy, Jokela type | MGI:1261428 | Mus musculus (house mouse) | 14004 | Chchd2 |
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| DOID:0081358 | epidermolytic hyperkeratosis 1 | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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| DOID:0081358 | epidermolytic hyperkeratosis 1 | MGI:96698 | Mus musculus (house mouse) | 16678 | Krt1 |
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| DOID:0081359 | epidermolytic hyperkeratosis 2 | HGNC:6413 | Homo sapiens (human) | 3858 | KRT10 |
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| DOID:0081360 | spastic quadriplegic cerebral palsy 2 | HGNC:19309 | Homo sapiens (human) | 23189 | KANK1 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | RGD:2041 | Rattus norvegicus (Norway rat) | 24170 | Add1 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:245 | Homo sapiens (human) | 120 | ADD3 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | MGI:87918 | Mus musculus (house mouse) | 11518 | Add1 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:244 | Homo sapiens (human) | 119 | ADD2 |
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| DOID:0081363 | distal myopathy with rimmed vacuoles | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0081363 | distal myopathy with rimmed vacuoles | MGI:107931 | Mus musculus (house mouse) | 18412 | Sqstm1 |
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| DOID:0081364 | neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0081364 | neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | MGI:107931 | Mus musculus (house mouse) | 18412 | Sqstm1 |
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| DOID:0081365 | Paget's disease of bone 2 | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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