HARS2

GENERAL INFORMATION

? »

Gene name

HARS2

Gene description

Histidyl-tRNA synthetase 2, mitochondrial

Protein class

Disease related genes
Enzymes
Mitochondrial proteins
Potential drug targets
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

5
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most of the normal tissues displayed moderate cytoplasmic positivity. Strong staining was for example observed in squamous epithelium, duodenum, pancreas, renal tubuli and testicular Leydig cells. Bile duct cells and myocytes were weakly stained or negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA035941
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Heart muscle

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

HARS2 (HGNC Symbol)

Synonyms

HARSL, HARSR, HO3

Description

Histidyl-tRNA synthetase 2, mitochondrial (HGNC Symbol)

Entrez gene summary

Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

Chromosome

5

Cytoband

q31.3

Chromosome location (bp)

140691426 - 140699291

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000112855 (version 78.38)

Entrez gene

23438

UniProt

P49590 (UniProt - Evidence at protein level)

neXtProt

NX_P49590

Antibodypedia

HARS2 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000230771
 
ENST00000448069
 
ENST00000503873
 
ENST00000508522
 
ENST00000509299
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HARS2-001 ENSP00000230771
ENST00000230771
P49590
Show all »
Show » Show » 506 56.9 Yes 0
HARS2-003 ENSP00000423616
ENST00000508522
P49590
Show all »
Show » Show » 481 54.1 Yes 0
HARS2-004 ENSP00000407105
ENST00000448069
B4DQ67
Show all »
Show » Show » 334 37.2 Yes 0
HARS2-008 ENSP00000424516
ENST00000503873
D6RB22
Show all »
Show » Show » 116 12.9 Yes 0
HARS2-009 ENSP00000425695
ENST00000509299
D6RJE6
Show all »
Show » Show » 181 20.6 Yes 0