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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:3132 | porphyria cutanea tarda | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:1742 | drug psychosis | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:1240 | leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:0080611 | anterior segment dysgenesis 6 | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0090122 | aromatase excess syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0080491 | cerebral cavernous malformation 1 | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0080489 | GM1 gangliosidosis type 3 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:1324 | lung cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:9256 | colorectal cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:583 | hemolytic anemia | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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