Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Genes search result for Homo sapiens
(View Results for all Objects and Ontologies)

3 records found for search term Fars2
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print GViewer Analysis Tools

RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1342814FARS2phenylalanyl-tRNA synthetase 2, mitochondrialThis gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative spli652499345771583Human278symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
16565332FARS2-AS1FARS2 antisense RNA 1INTERACTS WITH okadaic acid654524685458075Human1symbol , old_gene_name , COSMIC , name , Human Proteome Mapgene, ncrna, VALIDATED [RefSeq]
16565414AL022097.1novel transcript, antisense to FARS2656649855695272Humannamegene, ncrna, VALIDATED [RefSeq]