Incidental Mutation 'R2092:Fpr-rs4'
ID 231879
Institutional Source Beutler Lab
Gene Symbol Fpr-rs4
Ensembl Gene ENSMUSG00000048062
Gene Name formyl peptide receptor, related sequence 4
Synonyms
MMRRC Submission 040097-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # R2092 (G1)
Quality Score 217
Status Not validated
Chromosome 17
Chromosomal Location 18241995-18242966 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) CAGGAA to CA at 18242596 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000093311 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095651]
AlphaFold A4FUQ5
Predicted Effect probably null
Transcript: ENSMUST00000095651
SMART Domains Protein: ENSMUSP00000093311
Gene: ENSMUSG00000048062

DomainStartEndE-ValueType
Pfam:7tm_1 43 297 4.9e-35 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m T A 6: 121,651,896 (GRCm39) C1321* probably null Het
Abca8b A G 11: 109,857,534 (GRCm39) F673L possibly damaging Het
Adam19 T G 11: 45,951,731 (GRCm39) probably null Het
AI987944 T C 7: 41,024,041 (GRCm39) T313A possibly damaging Het
Akap13 A T 7: 75,260,318 (GRCm39) I178F probably benign Het
Alb G GA 5: 90,611,842 (GRCm39) probably null Het
Bod1l A G 5: 41,988,860 (GRCm39) S416P probably damaging Het
Casr A T 16: 36,330,405 (GRCm39) Y310N possibly damaging Het
Cela3a T C 4: 137,131,737 (GRCm39) N152S probably benign Het
Chrdl2 T A 7: 99,670,184 (GRCm39) C102* probably null Het
Col4a4 G A 1: 82,476,667 (GRCm39) S554L unknown Het
Col6a4 T C 9: 105,937,530 (GRCm39) K1392R probably damaging Het
Dab1 T G 4: 104,535,974 (GRCm39) Y128D probably damaging Het
Dars1 A T 1: 128,301,755 (GRCm39) M293K probably damaging Het
Dlec1 T C 9: 118,950,912 (GRCm39) F493L possibly damaging Het
Dmbt1 G T 7: 130,651,748 (GRCm39) W330L probably damaging Het
Dnah11 A T 12: 117,976,451 (GRCm39) M831K possibly damaging Het
Dock7 T C 4: 98,897,545 (GRCm39) N715S possibly damaging Het
Edc4 T A 8: 106,614,160 (GRCm39) L12Q probably damaging Het
Edem2 T C 2: 155,550,969 (GRCm39) M333V probably benign Het
Fto C A 8: 92,136,315 (GRCm39) Y194* probably null Het
Gnptab T G 10: 88,276,167 (GRCm39) Y1151* probably null Het
Grm1 A G 10: 10,564,969 (GRCm39) L1113P probably benign Het
Hnrnpa0 T C 13: 58,275,614 (GRCm39) K172E probably damaging Het
Ifitm1 A G 7: 140,549,427 (GRCm39) D70G probably damaging Het
Irx4 C A 13: 73,413,605 (GRCm39) T25K probably damaging Het
Kif22 C T 7: 126,632,802 (GRCm39) D195N probably damaging Het
Lrp2 C T 2: 69,366,365 (GRCm39) D245N probably benign Het
Lyz1 C T 10: 117,124,504 (GRCm39) R144Q probably benign Het
Macf1 T A 4: 123,276,971 (GRCm39) T6055S probably damaging Het
Mrgpra2b C T 7: 47,113,908 (GRCm39) V249I probably benign Het
Myh9 G A 15: 77,648,550 (GRCm39) Q80* probably null Het
Myo6 G T 9: 80,152,964 (GRCm39) R199L probably damaging Het
Naglu G A 11: 100,967,546 (GRCm39) V499I possibly damaging Het
Nfkbie T C 17: 45,869,465 (GRCm39) F140S probably benign Het
Or4p8 A G 2: 88,727,611 (GRCm39) F110S probably damaging Het
Or52ab7 G A 7: 102,978,316 (GRCm39) V208M probably damaging Het
Or52z1 A T 7: 103,437,279 (GRCm39) F68L possibly damaging Het
Or5b102 T A 19: 13,041,166 (GRCm39) Y130* probably null Het
Or5p81 CAAATA CA 7: 108,266,869 (GRCm39) probably null Het
Or8g21 A T 9: 38,906,485 (GRCm39) L82Q probably damaging Het
Otop1 A T 5: 38,457,110 (GRCm39) I290F probably damaging Het
P2rx2 C T 5: 110,489,007 (GRCm39) D203N probably damaging Het
Pcdhb10 T A 18: 37,547,240 (GRCm39) I772N probably benign Het
Pnliprp1 A G 19: 58,729,616 (GRCm39) H423R probably benign Het
Ptk2 A T 15: 73,108,040 (GRCm39) Y56* probably null Het
Rapgef3 T C 15: 97,658,604 (GRCm39) D134G probably damaging Het
Scaf11 A C 15: 96,313,708 (GRCm39) S1358A probably damaging Het
Scn9a T C 2: 66,363,720 (GRCm39) M844V probably damaging Het
Sh3tc1 T C 5: 35,858,002 (GRCm39) E1121G probably damaging Het
Slc25a15 T C 8: 22,870,950 (GRCm39) T176A probably damaging Het
Slc29a4 T A 5: 142,704,610 (GRCm39) I384N probably damaging Het
Slc40a1 A T 1: 45,948,614 (GRCm39) D555E probably benign Het
Smc5 T C 19: 23,216,263 (GRCm39) I446V probably benign Het
St6gal2 T C 17: 55,817,267 (GRCm39) Y477H probably damaging Het
Syngr1 A T 15: 80,000,141 (GRCm39) Q84L possibly damaging Het
Tedc1 T C 12: 113,121,340 (GRCm39) L187P probably damaging Het
Tg A G 15: 66,721,456 (GRCm39) I322V probably null Het
Thap12 T C 7: 98,365,656 (GRCm39) V608A possibly damaging Het
Tmbim6 T C 15: 99,299,949 (GRCm39) S22P probably damaging Het
Ttc3 C T 16: 94,243,691 (GRCm39) P1232S probably benign Het
Upk3a A G 15: 84,902,286 (GRCm39) T38A probably damaging Het
Utrn A T 10: 12,554,442 (GRCm39) M1549K probably benign Het
Vmn1r176 C T 7: 23,534,578 (GRCm39) D192N probably damaging Het
Vmn1r198 A G 13: 22,538,885 (GRCm39) T35A possibly damaging Het
Xkr7 C T 2: 152,895,983 (GRCm39) S279L probably damaging Het
Zer1 G A 2: 29,998,286 (GRCm39) L342F probably damaging Het
Zfp641 G T 15: 98,191,593 (GRCm39) T31N probably benign Het
Zfp74 G A 7: 29,653,349 (GRCm39) probably benign Het
Other mutations in Fpr-rs4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00539:Fpr-rs4 APN 17 18,242,188 (GRCm39) missense probably damaging 1.00
IGL01064:Fpr-rs4 APN 17 18,242,779 (GRCm39) missense probably damaging 1.00
IGL01626:Fpr-rs4 APN 17 18,242,493 (GRCm39) missense probably damaging 0.97
IGL02544:Fpr-rs4 APN 17 18,242,473 (GRCm39) missense probably benign
IGL02837:Fpr-rs4 UTSW 17 18,242,513 (GRCm39) missense probably benign 0.00
R0179:Fpr-rs4 UTSW 17 18,242,289 (GRCm39) nonsense probably null
R0383:Fpr-rs4 UTSW 17 18,242,359 (GRCm39) missense probably damaging 1.00
R0686:Fpr-rs4 UTSW 17 18,242,613 (GRCm39) missense probably benign 0.05
R1551:Fpr-rs4 UTSW 17 18,242,589 (GRCm39) missense possibly damaging 0.89
R1956:Fpr-rs4 UTSW 17 18,242,518 (GRCm39) missense probably damaging 0.97
R2040:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2041:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2043:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2045:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2048:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2093:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R2136:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R3624:Fpr-rs4 UTSW 17 18,242,596 (GRCm39) frame shift probably null
R4684:Fpr-rs4 UTSW 17 18,242,446 (GRCm39) missense probably damaging 1.00
R6076:Fpr-rs4 UTSW 17 18,242,317 (GRCm39) missense probably damaging 1.00
R6247:Fpr-rs4 UTSW 17 18,242,748 (GRCm39) missense probably benign 0.00
R6639:Fpr-rs4 UTSW 17 18,242,394 (GRCm39) nonsense probably null
R6757:Fpr-rs4 UTSW 17 18,242,394 (GRCm39) nonsense probably null
R8703:Fpr-rs4 UTSW 17 18,242,332 (GRCm39) missense probably damaging 0.99
R9007:Fpr-rs4 UTSW 17 18,242,416 (GRCm39) missense probably damaging 1.00
R9318:Fpr-rs4 UTSW 17 18,242,217 (GRCm39) missense probably benign
R9357:Fpr-rs4 UTSW 17 18,242,211 (GRCm39) missense probably damaging 0.97
R9435:Fpr-rs4 UTSW 17 18,242,391 (GRCm39) missense probably benign 0.00
Z1088:Fpr-rs4 UTSW 17 18,242,956 (GRCm39) missense probably benign 0.16
Z1088:Fpr-rs4 UTSW 17 18,242,181 (GRCm39) missense possibly damaging 0.85
Predicted Primers PCR Primer
(F):5'- CAGAAAAGTGGTTCTTGGAGC -3'
(R):5'- AAGCCAAGGTATTTGCTGGG -3'

Sequencing Primer
(F):5'- AGCTTGGATATTTGCTCTGCTGC -3'
(R):5'- CCAAGGTATTTGCTGGGTTAACCAAC -3'
Posted On 2014-09-18