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:0111564 | hypoplastic or aplastic tibia with polydactyly | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:2377 | multiple sclerosis | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:0050784 | primary progressive multiple sclerosis | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:9253 | gastrointestinal stromal tumor | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:13608 | biliary atresia | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:9282 | ocular hypertension | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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DOID:9452 | steatotic liver disease | HGNC:10840 | Homo sapiens (human) | 6464 | SHC1 |
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DOID:0050851 | glomerulosclerosis | HGNC:10840 | Homo sapiens (human) | 6464 | SHC1 |
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DOID:1168 | familial hyperlipidemia | HGNC:10840 | Homo sapiens (human) | 6464 | SHC1 |
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DOID:684 | hepatocellular carcinoma | HGNC:10840 | Homo sapiens (human) | 6464 | SHC1 |
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DOID:1380 | endometrial cancer | HGNC:10839 | Homo sapiens (human) | 6462 | SHBG |
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DOID:9352 | type 2 diabetes mellitus | HGNC:10839 | Homo sapiens (human) | 6462 | SHBG |
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DOID:9351 | diabetes mellitus | HGNC:10839 | Homo sapiens (human) | 6462 | SHBG |
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DOID:3070 | high grade glioma | HGNC:10830 | Homo sapiens (human) | 6455 | SH3GL1 |
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DOID:9119 | acute myeloid leukemia | HGNC:10830 | Homo sapiens (human) | 6455 | SH3GL1 |
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DOID:1856 | cherubism | HGNC:10825 | Homo sapiens (human) | 6452 | SH3BP2 |
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DOID:0060705 | X-linked lymphoproliferative syndrome 1 | HGNC:10820 | Homo sapiens (human) | 4068 | SH2D1A |
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DOID:0111395 | mucopolysaccharidosis type IIIA | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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DOID:1184 | nephrotic syndrome | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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DOID:9970 | obesity | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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DOID:9884 | muscular dystrophy | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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DOID:0050700 | cardiomyopathy | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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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