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Gene: AIMP2 (aminoacyl tRNA synthetase complex interacting multifunctional protein 2) Homo sapiens
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Symbol: AIMP2
Name: aminoacyl tRNA synthetase complex interacting multifunctional protein 2
Description: Predicted to have molecular adaptor activity. Predicted to be involved in tRNA aminoacylation for protein translation. Localizes to the aminoacyl-tRNA synthetase multienzyme complex and cytosol. Implicated in hypomyelinating leukodystrophy.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: aminoacyl tRNA synthase complex-interacting multifunctional protein 2; aminoacyl tRNA synthetase complex-interacting multifunctional protein 2; ARS-interacting multi-functional protein 2; HLD17; JTV-1; JTV1; multisynthase complex auxiliary component p38; multisynthetase complex auxiliary component p38; P38; PRO0992
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3876,009,245 - 6,023,834 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3776,048,882 - 6,063,465 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3676,015,408 - 6,029,991 (+)NCBINCBI36hg18NCBI36
Celera76,673,238 - 6,687,807 (-)NCBI
Cytogenetic Map7p22.1NCBI
HuRef75,920,617 - 5,935,248 (+)NCBIHuRef
CHM1_176,048,601 - 6,063,172 (+)NCBICHM1_1
CRA_TCAGchr7v276,095,227 - 6,109,810 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AIMP2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1603320
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-11-26
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.