Incidental Mutation 'R7504:Nars'
ID581694
Institutional Source Beutler Lab
Gene Symbol Nars
Ensembl Gene ENSMUSG00000024587
Gene Nameasparaginyl-tRNA synthetase
SynonymsASNRS
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.964) question?
Stock #R7504 (G1)
Quality Score225.009
Status Validated
Chromosome18
Chromosomal Location64499665-64516557 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 64512022 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Valine at position 52 (F52V)
Ref Sequence ENSEMBL: ENSMUSP00000025483 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025483]
Predicted Effect probably benign
Transcript: ENSMUST00000025483
AA Change: F52V

PolyPhen 2 Score 0.220 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000025483
Gene: ENSMUSG00000024587
AA Change: F52V

DomainStartEndE-ValueType
coiled coil region 80 112 N/A INTRINSIC
Pfam:tRNA_anti-codon 139 219 1.2e-12 PFAM
Pfam:tRNA-synt_2 236 554 1.8e-108 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (43/43)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. Asparaginyl-tRNA synthetase is localized to the cytoplasm and belongs to the class II family of tRNA synthetases. The N-terminal domain represents the signature sequence for the eukaryotic asparaginyl-tRNA synthetases. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600012H06Rik C G 17: 14,943,653 A14G probably damaging Het
6430573F11Rik A C 8: 36,512,155 N304T probably benign Het
Btn1a1 A T 13: 23,461,716 M161K probably benign Het
Camkk2 G A 5: 122,746,308 T350I probably damaging Het
Cdc42bpg C A 19: 6,306,784 D23E possibly damaging Het
Cdkn1a T C 17: 29,098,514 L36P probably damaging Het
Dek A G 13: 47,088,035 I351T probably damaging Het
Dst T C 1: 34,201,017 Y1816H probably damaging Het
Efl1 T A 7: 82,683,049 N300K probably damaging Het
Ephx2 A G 14: 66,101,617 Y294H probably damaging Het
Fancd2 T A 6: 113,545,038 I198N probably damaging Het
Gm6502 G T 5: 94,317,047 V431L probably benign Het
Grid1 G T 14: 35,562,513 A738S probably damaging Het
Gsx2 G A 5: 75,076,399 probably null Het
Hc G A 2: 35,061,319 T22I not run Het
Hps1 T C 19: 42,766,720 D261G probably benign Het
Ift80 T C 3: 68,918,005 Y539C probably damaging Het
Insc G T 7: 114,791,298 probably null Het
Isg15 T C 4: 156,200,045 M9V probably damaging Het
Kalrn A G 16: 34,256,233 L695P unknown Het
Nmt1 T G 11: 103,056,459 F225V probably damaging Het
Olfr1352 A G 10: 78,984,660 Y290C possibly damaging Het
Olfr143 A T 9: 38,254,243 K272N possibly damaging Het
Olfr1495 T A 19: 13,768,732 I130N probably damaging Het
Pbx3 T C 2: 34,175,924 T385A probably damaging Het
Pcdhb11 A T 18: 37,421,799 T61S probably benign Het
Rab11fip1 T C 8: 27,152,953 E606G possibly damaging Het
Rnf216 A G 5: 143,075,759 Y589H probably benign Het
Scara3 A G 14: 65,931,331 I279T possibly damaging Het
Sdk2 T A 11: 113,867,967 Y477F possibly damaging Het
Secisbp2l T C 2: 125,758,171 K415E probably benign Het
Stag1 C T 9: 100,888,328 T639I probably benign Het
Sv2b A T 7: 75,136,383 F430I probably benign Het
Tenm2 C T 11: 36,139,743 C743Y probably damaging Het
Tet2 C A 3: 133,487,339 V445L probably benign Het
Tmem132c T C 5: 127,554,632 S652P probably damaging Het
Togaram1 A G 12: 64,992,617 D1155G possibly damaging Het
Traip T C 9: 107,961,544 I169T probably benign Het
Usp45 T G 4: 21,816,892 M374R possibly damaging Het
Vmn2r81 A T 10: 79,268,332 H263L probably benign Het
Wdr95 T C 5: 149,581,846 V364A probably damaging Het
Zfp128 G A 7: 12,890,478 D258N probably damaging Het
Zfp335 G A 2: 164,909,418 T76I probably benign Het
Zfp688 C A 7: 127,419,311 C214F probably damaging Het
Zfp760 T C 17: 21,722,674 S277P probably damaging Het
Other mutations in Nars
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01012:Nars APN 18 64504968 missense probably damaging 1.00
IGL01962:Nars APN 18 64510483 missense probably benign 0.00
IGL01968:Nars APN 18 64507858 missense probably damaging 1.00
IGL02288:Nars APN 18 64510535 splice site probably benign
IGL02366:Nars APN 18 64503528 missense possibly damaging 0.70
IGL02948:Nars APN 18 64505195 missense possibly damaging 0.66
FR4976:Nars UTSW 18 64510445 critical splice donor site probably benign
R0591:Nars UTSW 18 64500567 missense probably damaging 1.00
R1654:Nars UTSW 18 64512049 missense probably damaging 1.00
R1691:Nars UTSW 18 64516414 critical splice donor site probably null
R1954:Nars UTSW 18 64500564 missense probably damaging 1.00
R2006:Nars UTSW 18 64505028 missense probably damaging 1.00
R2516:Nars UTSW 18 64505016 missense probably damaging 1.00
R3433:Nars UTSW 18 64509303 missense probably damaging 1.00
R4378:Nars UTSW 18 64501353 missense probably damaging 1.00
R4667:Nars UTSW 18 64505231 missense possibly damaging 0.93
R4737:Nars UTSW 18 64516427 missense probably benign
R4877:Nars UTSW 18 64500572 nonsense probably null
R5950:Nars UTSW 18 64510485 missense possibly damaging 0.91
R6434:Nars UTSW 18 64507801 missense probably benign 0.01
R6920:Nars UTSW 18 64501400 missense probably damaging 0.99
R7082:Nars UTSW 18 64504354 missense possibly damaging 0.68
R7132:Nars UTSW 18 64507770 critical splice donor site probably null
R8120:Nars UTSW 18 64504351 missense probably benign 0.19
R8343:Nars UTSW 18 64504387 missense probably benign 0.01
R8429:Nars UTSW 18 64501320 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGCAAATTCATCAGTCACCTC -3'
(R):5'- CTGCTGACATGGTCTTTGCC -3'

Sequencing Primer
(F):5'- AGAGTCGTTCTTCATCTGTTCTCTG -3'
(R):5'- GACATGGTCTTTGCCTCTCGG -3'
Posted On2019-10-17