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Gene: TRR-TCT3-1 (tRNA-Arg (anticodon TCT) 3-1) Homo sapiens
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Symbol: TRR-TCT3-1
Name: tRNA-Arg (anticodon TCT) 3-1
Description: ASSOCIATED WITH early infantile epileptic encephalopathy; primary coenzyme Q10 deficiency 7
Type: trna
RefSeq Status: MODEL
Also known as: transfer RNA-Arg (TCT) 3-1; TRNAR12; TRR-TCT3-2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389128,340,076 - 128,340,166 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh379131,102,355 - 131,102,445 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map9q34.11NCBI
HuRef9100,715,179 - 100,715,269 (-)NCBIHuRef
CHM1_19131,253,391 - 131,253,481 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on TRR-TCT3-1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 2300868
Created: 2008-09-19
Species: Homo sapiens
Last Modified: 2019-12-25
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.