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:5426 | primary ovarian insufficiency | HGNC:17675 | Homo sapiens (human) | 57510 | XPO5 |
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DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:9669 | senile cataract | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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DOID:9993 | hypoglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6637 | Homo sapiens (human) | 4001 | LMNB1 |
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DOID:9256 | colorectal cancer | HGNC:9645 | Homo sapiens (human) | 5782 | PTPN12 |
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DOID:4450 | renal cell carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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DOID:0111726 | geleophysic dysplasia 2 | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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DOID:10763 | hypertension | HGNC:7200 | Homo sapiens (human) | 4343 | MOV10 |
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DOID:5295 | intestinal disease | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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DOID:12236 | primary biliary cholangitis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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DOID:9164 | achalasia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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DOID:0112167 | autosomal dominant nonsyndromic deafness 76 | HGNC:9090 | Homo sapiens (human) | 5357 | PLS1 |
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DOID:13025 | retinopathy of prematurity | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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DOID:12849 | autistic disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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DOID:3393 | coronary artery disease | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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DOID:5082 | liver cirrhosis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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DOID:0080533 | Carney-Stratakis syndrome | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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DOID:1070 | primary open angle glaucoma | HGNC:11785 | Homo sapiens (human) | 7057 | THBS1 |
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DOID:1793 | pancreatic cancer | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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DOID:0080722 | Kenny-Caffey syndrome type 1 | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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DOID:1059 | intellectual disability | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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DOID:10763 | hypertension | RGD:61925 | Rattus norvegicus (Norway rat) | 29340 | Prkce |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024