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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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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 | July 29, 2024 |
| Disease ID ▲ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0060639 | permanent neonatal diabetes mellitus | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060639 | permanent neonatal diabetes mellitus | Xenbase:XB-GENE-864803 | Xenopus laevis (African clawed frog) | 378695 | ins.L |
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| DOID:0060639 | permanent neonatal diabetes mellitus | Xenbase:XB-GENE-6252363 | Xenopus laevis (African clawed frog) | 378696 | ins.S |
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| DOID:0060639 | permanent neonatal diabetes mellitus | ZFIN:ZDB-GENE-980526-110 | Danio rerio (zebrafish) | 30262 | ins |
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| DOID:0060639 | permanent neonatal diabetes mellitus | RGD:2915 | Rattus norvegicus (Norway rat) | 24505 | Ins1 |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060643 | primary sclerosing cholangitis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:0060643 | primary sclerosing cholangitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | SGD:S000003052 | Saccharomyces cerevisiae S288C | 852796 | GUP1 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | MGI:96545 | Mus musculus (house mouse) | 16177 | Il1r1 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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| DOID:0060669 | cerebral cavernous malformation | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0060673 | Peters anomaly | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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