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:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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DOID:3910 | lung adenocarcinoma | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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DOID:1612 | breast cancer | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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DOID:3910 | lung adenocarcinoma | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:9256 | colorectal cancer | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:9952 | acute lymphoblastic leukemia | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:684 | hepatocellular carcinoma | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:0081155 | common variable immunodeficiency 13 | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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DOID:0060041 | autism spectrum disorder | HGNC:6494 | Homo sapiens (human) | 10319 | LAMC3 |
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DOID:1793 | pancreatic cancer | HGNC:920 | Homo sapiens (human) | 10317 | B3GALT5 |
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DOID:9970 | obesity | HGNC:4518 | Homo sapiens (human) | 10316 | NMUR1 |
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DOID:0110765 | hereditary spastic paraplegia 12 | HGNC:10469 | Homo sapiens (human) | 10313 | RTN3 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:10469 | Homo sapiens (human) | 10313 | RTN3 |
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DOID:0112236 | lissencephaly 6 | HGNC:6217 | Homo sapiens (human) | 10300 | KATNB1 |
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DOID:10907 | microcephaly | HGNC:6217 | Homo sapiens (human) | 10300 | KATNB1 |
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DOID:0060250 | idiopathic scoliosis | HGNC:6217 | Homo sapiens (human) | 10300 | KATNB1 |
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DOID:0060257 | dyschromatosis symmetrica hereditaria | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:5082 | liver cirrhosis | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:11166 | Human papillomavirus infectious disease | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:0050629 | Aicardi-Goutieres syndrome | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:10534 | stomach cancer | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:3744 | cervical squamous cell carcinoma | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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DOID:14330 | Parkinson's disease | HGNC:16059 | Homo sapiens (human) | 10298 | PAK4 |
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DOID:4467 | clear cell renal cell carcinoma | HGNC:16059 | Homo sapiens (human) | 10298 | PAK4 |
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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