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 |
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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 |
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DOID:76 | stomach disease | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:0080191 | PTEN hamartoma tumor syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:10584 | retinitis pigmentosa | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:3742 | bladder squamous cell carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:6457 | Cowden syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:8719 | in situ carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:3070 | high grade glioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:1612 | breast cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:2394 | ovarian cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:9256 | colorectal cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:2938 | Epstein-Barr virus infectious disease | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:303 | substance-related disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:10534 | stomach cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:13042 | persistent fetal circulation syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:264 | hemangiopericytoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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DOID:3211 | lysosomal storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:9455 | lipid storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:10587 | Krabbe disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:10581 | metachromatic leukodystrophy | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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DOID:987 | alopecia | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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DOID:8634 | prostate carcinoma in situ | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024