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 | October 9, 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:2218 | blood platelet disease | HGNC:12013 | Homo sapiens (human) | 7171 | TPM4 |
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DOID:1289 | neurodegenerative disease | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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DOID:2978 | carbohydrate metabolic disorder | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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DOID:162 | cancer | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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DOID:0050884 | triosephosphate isomerase deficiency | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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DOID:9282 | ocular hypertension | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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DOID:1596 | depressive disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:10930 | borderline personality disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:1574 | alcohol use disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:9478 | postpartum depression | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:1094 | attention deficit hyperactivity disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:10652 | Alzheimer's disease | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:0060041 | autism spectrum disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:5419 | schizophrenia | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:0060249 | scoliosis | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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DOID:0060412 | chromosome 1q41-q42 deletion syndrome | HGNC:12000 | Homo sapiens (human) | 7159 | TP53BP2 |
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DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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DOID:6432 | pulmonary hypertension | HGNC:11999 | Homo sapiens (human) | 7158 | TP53BP1 |
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DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:3702 | cervical adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:0050834 | CHARGE syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:0050866 | oral squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:0112182 | mismatch repair cancer syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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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 v4.1.0
Last updated: December 9, 2024