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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:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:4621 | holoprosencephaly | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
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| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | HGNC:8960 | Homo sapiens (human) | 5279 | PIGC |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:10112 | sleeping sickness | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000004263 | Saccharomyces cerevisiae S288C | 850979 | PIG1 |
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| DOID:1574 | alcohol use disorder | SGD:S000004263 | Saccharomyces cerevisiae S288C | 850979 | PIG1 |
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| DOID:162 | cancer | FB:FBgn0266438 | Drosophila melanogaster (fruit fly) | 19835548 | PIG-Z |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | FB:FBgn0265174 | Drosophila melanogaster (fruit fly) | 19835383 | PIG-V |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | FB:FBgn0035464 | Drosophila melanogaster (fruit fly) | 38446 | PIG-B |
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| DOID:10112 | sleeping sickness | FB:FBgn0035464 | Drosophila melanogaster (fruit fly) | 38446 | PIG-B |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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