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:4450 | renal cell carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:8991 | cervix uteri carcinoma in situ | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:0080764 | hereditary diffuse gastric cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:0080345 | blepharocheilodontic syndrome 1 | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:1612 | breast cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:1380 | endometrial cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:687 | hepatoblastoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:2394 | ovarian cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:3770 | pulmonary fibrosis | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:4531 | mucoepidermoid carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:0050866 | oral squamous cell carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:3910 | lung adenocarcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:9296 | cleft lip | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:9351 | diabetes mellitus | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:3969 | thyroid gland papillary carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:9119 | acute myeloid leukemia | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:684 | hepatocellular carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:3457 | invasive lobular carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:11054 | urinary bladder cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:0090003 | agenesis of the corpus callosum with peripheral neuropathy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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DOID:1826 | epilepsy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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DOID:2477 | motor peripheral neuropathy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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DOID:2843 | long QT syndrome | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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DOID:0050650 | familial atrial fibrillation | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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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