SARS2

GENERAL INFORMATION

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Gene name

SARS2

Gene description

Seryl-tRNA synthetase 2, mitochondrial

Protein class

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

Predicted localization

Intracellular

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Not detected

Protein evidence

Evidence at protein level

Protein localization

General granular cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation. Caution, targets protein from more than one gene.

Data reliability

Supportive based on 2 antibodies.
HPA052730 , HPA056957
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Not detected

Organ

Expression



GENE INFORMATION

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Gene name

SARS2 (HGNC Symbol)

Synonyms

FLJ20450, mtSerRS, SARS, SARSM, SerRSmt, SERS, SYS

Description

Seryl-tRNA synthetase 2, mitochondrial (HGNC Symbol)

Entrez gene summary

This gene encodes the mitochondrial seryl-tRNA synthethase precursor, a member of the class II tRNA synthetase family. The mature enzyme catalyzes the ligation of Serine to tRNA(Ser) and participates in the biosynthesis of selenocysteinyl-tRNA(sec) in mitochondria. The enzyme contains an N-terminal tRNA binding domain and a core catalytic domain. It functions in a homodimeric form, which is stabilized by tRNA binding. This gene is regulated by a bidirectional promoter that also controls the expression of mitochondrial ribosomal protein S12. Both genes are within the critical interval for the autosomal dominant deafness locus DFNA4 and might be linked to this disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Mar 2009]

Chromosome

19

Cytoband

q13.2

Chromosome location (bp)

38915266 - 38930896

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000104835 (version 78.38)

Entrez gene

54938

UniProt

Q9NP81 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NP81

Antibodypedia

SARS2 antibodies


PROTEIN BROWSER

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ENST00000221431
 
ENST00000430193
 
ENST00000594171
 
ENST00000598831
 
ENST00000600042
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SARS2-001 ENSP00000221431
ENST00000221431
Q9NP81
Show all »
Show » Show » 518 58.3 No 0
SARS2-003 ENSP00000472847
ENST00000600042
Q9NP81
Show all »
Show » Show » 520 58 No 0
SARS2-005 ENSP00000406754
ENST00000430193
M0QWZ7
Show all »
Show » Show » 518 58.2 No 0
SARS2-006 ENSP00000472339
ENST00000594171
M0R259
Show all »
Show » Show » 328 36.4 No 0
SARS2-014 ENSP00000468865
ENST00000598831
M0QX29
Show all »
Show » Show » 187 20.5 No 0