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:1682 | congenital heart disease | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:10534 | stomach cancer | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:0050866 | oral squamous cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:1520 | colon carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:10941 | intracranial aneurysm | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:0080598 | Kleefstra syndrome 2 | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:10283 | prostate cancer | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:3969 | thyroid gland papillary carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:0060473 | Kabuki syndrome | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:3907 | lung squamous cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:5409 | lung small cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:1612 | breast cancer | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:3908 | lung non-small cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:3459 | breast carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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DOID:0050696 | fetal alcohol spectrum disorder | HGNC:30412 | Homo sapiens (human) | 80854 | SETD7 |
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DOID:13619 | extrahepatic cholestasis | HGNC:30412 | Homo sapiens (human) | 80854 | SETD7 |
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DOID:0050602 | triple-A syndrome | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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DOID:9164 | achalasia | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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DOID:0060041 | autism spectrum disorder | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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DOID:0081343 | congenital myopathy 9A | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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DOID:0081344 | congenital myopathy 9B | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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DOID:14261 | fragile X syndrome | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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DOID:7474 | malignant pleural mesothelioma | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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DOID:0081151 | common variable immunodeficiency 8 | MGI:1933162 | Mus musculus (house mouse) | 80877 | Lrba |
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DOID:0060041 | autism spectrum disorder | MGI:1933162 | Mus musculus (house mouse) | 80877 | Lrba |
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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