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:8947 | diabetic retinopathy | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:332 | amyotrophic lateral sclerosis | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:2945 | severe acute respiratory syndrome | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:2055 | post-traumatic stress disorder | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:12930 | dilated cardiomyopathy | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:10763 | hypertension | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:1793 | pancreatic cancer | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:224 | transient cerebral ischemia | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:11650 | bronchopulmonary dysplasia | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:9256 | colorectal cancer | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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DOID:746 | adenomatoid tumor | HGNC:20456 | Homo sapiens (human) | 84231 | TRAF7 |
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DOID:684 | hepatocellular carcinoma | HGNC:20456 | Homo sapiens (human) | 84231 | TRAF7 |
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DOID:1788 | peritoneal mesothelioma | HGNC:20456 | Homo sapiens (human) | 84231 | TRAF7 |
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DOID:0111437 | optic atrophy 7 | HGNC:25382 | Homo sapiens (human) | 84233 | TMEM126A |
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DOID:0070139 | autosomal recessive cutis laxa type IC | HGNC:6717 | Homo sapiens (human) | 8425 | LTBP4 |
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DOID:3144 | cutis laxa | HGNC:6717 | Homo sapiens (human) | 8425 | LTBP4 |
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DOID:0081328 | familial hyperinsulinemic hypoglycemia 8 | HGNC:29681 | Homo sapiens (human) | 84275 | SLC25A33 |
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DOID:0060669 | cerebral cavernous malformation | HGNC:11403 | Homo sapiens (human) | 8428 | STK24 |
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DOID:6000 | congestive heart failure | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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DOID:0080199 | colorectal carcinoma | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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DOID:684 | hepatocellular carcinoma | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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DOID:9119 | acute myeloid leukemia | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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DOID:0050681 | Borjeson-Forssman-Lehmann syndrome | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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DOID:9955 | hypoplastic left heart syndrome | HGNC:28184 | Homo sapiens (human) | 84303 | CHCHD6 |
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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