Incidental Mutation 'R7824:Farsb'
ID 602049
Institutional Source Beutler Lab
Gene Symbol Farsb
Ensembl Gene ENSMUSG00000026245
Gene Name phenylalanyl-tRNA synthetase, beta subunit
Synonyms Farslb, Farsl, Frsb, PheRS alpha
MMRRC Submission 045878-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.971) question?
Stock # R7824 (G1)
Quality Score 225.009
Status Validated
Chromosome 1
Chromosomal Location 78394612-78465534 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 78445936 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 148 (N148D)
Ref Sequence ENSEMBL: ENSMUSP00000139933 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068333] [ENSMUST00000170217] [ENSMUST00000188247] [ENSMUST00000189529] [ENSMUST00000190441]
AlphaFold Q9WUA2
Predicted Effect probably benign
Transcript: ENSMUST00000068333
AA Change: N247D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000069508
Gene: ENSMUSG00000026245
AA Change: N247D

DomainStartEndE-ValueType
Blast:B3_4 56 95 6e-14 BLAST
B3_4 117 279 3.29e-29 SMART
B5 304 374 6.31e-17 SMART
SCOP:d1jjcb5 377 586 1e-36 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000170217
AA Change: N247D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000129828
Gene: ENSMUSG00000026245
AA Change: N247D

DomainStartEndE-ValueType
Blast:B3_4 56 95 6e-14 BLAST
B3_4 117 279 3.29e-29 SMART
B5 304 374 6.31e-17 SMART
SCOP:d1jjcb5 377 586 1e-36 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000188247
AA Change: N148D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000139933
Gene: ENSMUSG00000026245
AA Change: N148D

DomainStartEndE-ValueType
B3_4 18 180 2.5e-33 SMART
SCOP:d1jjcb2 204 237 3e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000189529
SMART Domains Protein: ENSMUSP00000140001
Gene: ENSMUSG00000026245

DomainStartEndE-ValueType
PDB:3L4G|P 1 38 3e-20 PDB
Predicted Effect probably benign
Transcript: ENSMUST00000190441
SMART Domains Protein: ENSMUSP00000140934
Gene: ENSMUSG00000026245

DomainStartEndE-ValueType
Blast:B3_4 89 128 3e-15 BLAST
Pfam:B3_4 150 206 1e-5 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.5%
Validation Efficiency 100% (65/65)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a highly conserved enzyme that belongs to the aminoacyl-tRNA synthetase class IIc subfamily. This enzyme comprises the regulatory beta subunits that form a tetramer with two catalytic alpha subunits. In the presence of ATP, this tetramer is responsible for attaching L-phenylalanine to the terminal adenosine of the appropriate tRNA. A pseudogene located on chromosome 10 has been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]
Allele List at MGI

All alleles(15) : Targeted(2) Gene trapped(13)

Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Apol7a T C 15: 77,273,275 (GRCm39) R396G probably damaging Het
Arhgap40 A T 2: 158,376,666 (GRCm39) R267S probably damaging Het
Asb5 A C 8: 55,037,827 (GRCm39) H173P Het
Atp6v0a2 A G 5: 124,779,443 (GRCm39) E186G probably damaging Het
Bbs2 A T 8: 94,816,388 (GRCm39) probably null Het
Bub1b T G 2: 118,457,448 (GRCm39) probably null Het
Capn7 A G 14: 31,074,367 (GRCm39) T257A probably benign Het
Chrna6 T C 8: 27,897,392 (GRCm39) I162V probably damaging Het
Cldn6 T A 17: 23,900,581 (GRCm39) C182S probably damaging Het
Cyp2f2 G A 7: 26,828,678 (GRCm39) V183I probably benign Het
Cysltr2 A G 14: 73,267,203 (GRCm39) I169T probably benign Het
Ddx11 T C 17: 66,437,543 (GRCm39) probably null Het
Efhc1 A T 1: 21,049,685 (GRCm39) Y515F probably damaging Het
Fmnl2 C T 2: 52,963,692 (GRCm39) L275F unknown Het
Gfpt2 T G 11: 49,715,268 (GRCm39) I421R probably damaging Het
Gm8297 A G 14: 16,167,939 (GRCm39) N193S possibly damaging Het
Hic1 C T 11: 75,057,042 (GRCm39) V616M possibly damaging Het
Ica1l T G 1: 60,047,029 (GRCm39) M241L probably benign Het
Ighg3 A T 12: 113,323,426 (GRCm39) D283E Het
Ing1 A G 8: 11,611,814 (GRCm39) E178G probably benign Het
Ism2 A C 12: 87,326,634 (GRCm39) V435G probably damaging Het
Klhdc2 A G 12: 69,354,002 (GRCm39) H271R probably damaging Het
Lama1 T A 17: 68,111,468 (GRCm39) S2240T Het
Lrp2 T A 2: 69,331,883 (GRCm39) E1624V possibly damaging Het
Map3k21 C G 8: 126,637,702 (GRCm39) P96R probably benign Het
Mfge8 G T 7: 78,795,135 (GRCm39) probably null Het
Mical2 T A 7: 112,006,844 (GRCm39) Y588N probably damaging Het
Mrps15 A T 4: 125,945,170 (GRCm39) N119I probably damaging Het
Mybpc2 G A 7: 44,154,284 (GRCm39) probably null Het
Myo9a T A 9: 59,767,392 (GRCm39) H865Q probably damaging Het
Odf4 A T 11: 68,812,898 (GRCm39) S253R probably benign Het
Or6c5c A G 10: 129,298,665 (GRCm39) N40S probably damaging Het
Ovch2 A G 7: 107,388,295 (GRCm39) probably null Het
Pax8 A G 2: 24,325,913 (GRCm39) S324P possibly damaging Het
Plau A G 14: 20,892,393 (GRCm39) S393G probably benign Het
Primpol G T 8: 47,039,459 (GRCm39) P387Q probably damaging Het
Prph2 T C 17: 47,221,732 (GRCm39) L37S possibly damaging Het
Rapgefl1 A G 11: 98,741,980 (GRCm39) N648S probably damaging Het
Rin2 T A 2: 145,703,037 (GRCm39) S533T probably benign Het
Rsf1 CG CGACGGCGGGG 7: 97,229,115 (GRCm39) probably benign Het
Setd6 A T 8: 96,442,866 (GRCm39) H101L probably benign Het
Sez6 T C 11: 77,865,375 (GRCm39) S671P probably damaging Het
Slc22a3 G T 17: 12,683,350 (GRCm39) A171E probably damaging Het
Son T C 16: 91,453,416 (GRCm39) L721S probably damaging Het
Spata31d1b A T 13: 59,865,047 (GRCm39) R732W possibly damaging Het
Speg T A 1: 75,360,661 (GRCm39) probably null Het
Srd5a3 T A 5: 76,302,618 (GRCm39) F328I probably damaging Het
Tbc1d2 C T 4: 46,637,746 (GRCm39) probably null Het
Tfap2b G A 1: 19,304,531 (GRCm39) G447D probably damaging Het
Thoc3 A C 13: 54,611,591 (GRCm39) F232C probably damaging Het
Togaram2 T A 17: 72,011,746 (GRCm39) M476K probably benign Het
Tpgs2 G T 18: 25,262,922 (GRCm39) F232L probably benign Het
Ttll3 CAAAGTAA CAAAGTAAAGTAA 6: 113,376,118 (GRCm39) probably null Het
Tube1 A G 10: 39,018,294 (GRCm39) I124V probably benign Het
Ubr5 A T 15: 37,991,566 (GRCm39) H1992Q probably damaging Het
Utrn G A 10: 12,362,354 (GRCm39) R2660C probably damaging Het
Vcan T C 13: 89,836,773 (GRCm39) T2924A probably damaging Het
Vmn2r120 T C 17: 57,832,942 (GRCm39) Y79C probably damaging Het
Vwa8 T C 14: 79,275,587 (GRCm39) V790A probably benign Het
Vwf A G 6: 125,635,778 (GRCm39) K270E Het
Zfp874b A G 13: 67,622,093 (GRCm39) F402L probably benign Het
Other mutations in Farsb
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00092:Farsb APN 1 78,439,630 (GRCm39) missense probably benign 0.08
IGL01328:Farsb APN 1 78,447,729 (GRCm39) missense probably benign 0.02
IGL01801:Farsb APN 1 78,435,216 (GRCm39) missense probably benign 0.38
R0054:Farsb UTSW 1 78,439,011 (GRCm39) nonsense probably null
R0054:Farsb UTSW 1 78,439,011 (GRCm39) nonsense probably null
R1051:Farsb UTSW 1 78,420,287 (GRCm39) missense possibly damaging 0.49
R1769:Farsb UTSW 1 78,443,620 (GRCm39) missense probably benign 0.06
R4332:Farsb UTSW 1 78,445,903 (GRCm39) missense possibly damaging 0.61
R4664:Farsb UTSW 1 78,420,402 (GRCm39) missense possibly damaging 0.90
R4796:Farsb UTSW 1 78,401,833 (GRCm39) makesense probably null
R4859:Farsb UTSW 1 78,444,609 (GRCm39) missense probably benign 0.01
R5484:Farsb UTSW 1 78,452,833 (GRCm39) missense probably damaging 1.00
R5500:Farsb UTSW 1 78,447,761 (GRCm39) missense probably damaging 1.00
R5557:Farsb UTSW 1 78,445,888 (GRCm39) critical splice donor site probably null
R6109:Farsb UTSW 1 78,439,907 (GRCm39) critical splice donor site probably null
R6368:Farsb UTSW 1 78,443,602 (GRCm39) critical splice donor site probably null
R6720:Farsb UTSW 1 78,449,134 (GRCm39) missense probably damaging 1.00
R7166:Farsb UTSW 1 78,447,821 (GRCm39) missense probably benign
R7184:Farsb UTSW 1 78,458,994 (GRCm39) missense possibly damaging 0.86
R7233:Farsb UTSW 1 78,447,718 (GRCm39) critical splice donor site probably null
R7536:Farsb UTSW 1 78,420,391 (GRCm39) missense possibly damaging 0.89
R7753:Farsb UTSW 1 78,456,740 (GRCm39) missense probably benign 0.25
R7916:Farsb UTSW 1 78,435,200 (GRCm39) critical splice donor site probably null
R8120:Farsb UTSW 1 78,439,475 (GRCm39) missense probably benign 0.00
R8517:Farsb UTSW 1 78,439,933 (GRCm39) nonsense probably null
R8794:Farsb UTSW 1 78,401,678 (GRCm39) unclassified probably benign
R9131:Farsb UTSW 1 78,459,951 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- CTACATTTGTAGTAGCTGAAAGCAG -3'
(R):5'- GGAAATGATACATGCCCTATATCG -3'

Sequencing Primer
(F):5'- CCTGTATGAAGATCAATCAAGCTGC -3'
(R):5'- CATGCCCTATATCGAGGCATAGTTG -3'
Posted On 2019-12-03