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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:11054 | urinary bladder cancer | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:3459 | breast carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:8634 | prostate carcinoma in situ | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:4450 | renal cell carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0111626 | D-glyceric aciduria | MGI:2444085 | Mus musculus (house mouse) | 235582 | Glyctk |
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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:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:14219 | renal tubular acidosis | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:557 | kidney disease | MGI:2183549 | Mus musculus (house mouse) | 235435 | Lctl |
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| DOID:3650 | lactic acidosis | MGI:2385311 | Mus musculus (house mouse) | 235339 | Dlat |
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| DOID:3649 | pyruvate decarboxylase deficiency | MGI:2385311 | Mus musculus (house mouse) | 235339 | Dlat |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:0081122 | Catel Manzke syndrome | HGNC:20324 | Homo sapiens (human) | 23483 | TGDS |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:12858 | Huntington's disease | HGNC:9755 | Homo sapiens (human) | 23475 | QPRT |
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| DOID:0112315 | brain small vessel disease 3 | MGI:1924348 | Mus musculus (house mouse) | 234407 | Colgalt1 |
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| DOID:684 | hepatocellular carcinoma | MGI:2384588 | Mus musculus (house mouse) | 234258 | Neil3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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