Incidental Mutation 'R3963:Fpr-rs6'
ID 312212
Institutional Source Beutler Lab
Gene Symbol Fpr-rs6
Ensembl Gene ENSMUSG00000071275
Gene Name formyl peptide receptor, related sequence 6
Synonyms
MMRRC Submission 040932-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # R3963 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 20402340-20403359 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 20402479 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Leucine at position 294 (P294L)
Ref Sequence ENSEMBL: ENSMUSP00000093296 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095636]
AlphaFold Q3SXG2
Predicted Effect probably damaging
Transcript: ENSMUST00000095636
AA Change: P294L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000093296
Gene: ENSMUSG00000071275
AA Change: P294L

DomainStartEndE-ValueType
Pfam:7tm_1 43 297 5.7e-38 PFAM
Meta Mutation Damage Score 0.9282 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency 100% (61/61)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts18 T C 8: 114,504,443 (GRCm39) D59G probably benign Het
Ank2 A T 3: 126,728,245 (GRCm39) S783T probably benign Het
Arfgef3 T C 10: 18,468,025 (GRCm39) D1725G probably damaging Het
B3gnt5 A G 16: 19,587,798 (GRCm39) S6G probably benign Het
Btbd8 G A 5: 107,655,222 (GRCm39) C1007Y probably damaging Het
Ccdc82 C A 9: 13,252,011 (GRCm39) T101K possibly damaging Het
Ccdc85a A C 11: 28,526,396 (GRCm39) M376R probably benign Het
Cd200r1 T A 16: 44,613,158 (GRCm39) C255S probably benign Het
Cdc23 T C 18: 34,779,972 (GRCm39) M119V probably benign Het
Cers3 G T 7: 66,435,823 (GRCm39) A261S probably benign Het
Clptm1 C T 7: 19,372,121 (GRCm39) W238* probably null Het
Cr2 A G 1: 194,842,047 (GRCm39) V302A probably damaging Het
Cyp4a31 A G 4: 115,431,969 (GRCm39) probably benign Het
Dennd4a T A 9: 64,769,613 (GRCm39) I440N probably damaging Het
Dsc2 C T 18: 20,184,284 (GRCm39) V35I probably damaging Het
Dyrk1a T A 16: 94,464,605 (GRCm39) M71K probably benign Het
Exoc3l2 G A 7: 19,229,181 (GRCm39) G200S probably benign Het
Fhip2a T C 19: 57,361,442 (GRCm39) L122P possibly damaging Het
Fkbp15 A T 4: 62,258,914 (GRCm39) I114N probably damaging Het
Frmd6 A G 12: 70,940,638 (GRCm39) T428A probably benign Het
G6pd2 T A 5: 61,966,228 (GRCm39) M1K probably null Het
Gdf3 C T 6: 122,583,717 (GRCm39) V217I probably benign Het
Grm7 G T 6: 110,623,309 (GRCm39) V161F probably damaging Het
Gtf3c1 T C 7: 125,292,397 (GRCm39) probably null Het
Hrg G A 16: 22,774,825 (GRCm39) V152I possibly damaging Het
Itpkc T C 7: 26,926,934 (GRCm39) T327A probably damaging Het
Jade1 T C 3: 41,555,845 (GRCm39) V304A probably damaging Het
Leo1 C A 9: 75,357,762 (GRCm39) probably benign Het
Lrrc7 A T 3: 157,866,042 (GRCm39) L1233Q probably damaging Het
Ltbp3 G A 19: 5,804,050 (GRCm39) R854Q probably benign Het
Matn2 C A 15: 34,388,937 (GRCm39) Y342* probably null Het
Minar1 G A 9: 89,483,963 (GRCm39) T478I probably damaging Het
Mlh3 T C 12: 85,315,454 (GRCm39) H244R possibly damaging Het
Mmaa A T 8: 79,994,843 (GRCm39) V321E probably damaging Het
Ntng1 T A 3: 109,842,184 (GRCm39) L196F probably damaging Het
Oas1e A G 5: 120,932,205 (GRCm39) V146A probably damaging Het
Or52z1 G T 7: 103,437,241 (GRCm39) T81K probably benign Het
Plcxd2 T C 16: 45,800,864 (GRCm39) K120R probably damaging Het
Prex2 G T 1: 11,180,581 (GRCm39) C382F possibly damaging Het
Psg29 T A 7: 16,942,510 (GRCm39) H170Q probably benign Het
Ptprk A G 10: 28,427,661 (GRCm39) T747A probably damaging Het
Qki G A 17: 10,435,394 (GRCm39) probably benign Het
Rpusd2 A G 2: 118,869,085 (GRCm39) T503A probably benign Het
Rtn3 T C 19: 7,435,510 (GRCm39) S142G probably damaging Het
Slco1a5 C T 6: 142,194,370 (GRCm39) probably null Het
Snap91 A T 9: 86,657,665 (GRCm39) W509R probably damaging Het
Srsf3 C T 17: 29,255,430 (GRCm39) probably benign Het
Tmem267 A T 13: 119,629,175 (GRCm39) probably null Het
Tmem63a G A 1: 180,790,679 (GRCm39) D446N possibly damaging Het
Tnfaip8 C A 18: 50,223,653 (GRCm39) H154N possibly damaging Het
Trim35 T C 14: 66,541,503 (GRCm39) L209P probably damaging Het
Ttf1 A G 2: 28,954,816 (GRCm39) E60G possibly damaging Het
Ttf2 T C 3: 100,849,136 (GRCm39) probably benign Het
Tubg2 T C 11: 101,051,224 (GRCm39) probably null Het
Ubap1l C T 9: 65,276,477 (GRCm39) probably benign Het
Usp48 A T 4: 137,360,750 (GRCm39) R26* probably null Het
Vmn1r222 A G 13: 23,417,102 (GRCm39) V37A probably benign Het
Vmn2r4 T A 3: 64,322,572 (GRCm39) N49I probably damaging Het
Zfp979 A T 4: 147,697,588 (GRCm39) C374S probably benign Het
Other mutations in Fpr-rs6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02836:Fpr-rs6 APN 17 20,403,307 (GRCm39) missense probably benign 0.30
IGL03380:Fpr-rs6 APN 17 20,403,245 (GRCm39) missense possibly damaging 0.66
R0149:Fpr-rs6 UTSW 17 20,402,475 (GRCm39) missense probably benign 0.29
R0190:Fpr-rs6 UTSW 17 20,402,741 (GRCm39) missense probably benign 0.07
R1347:Fpr-rs6 UTSW 17 20,403,011 (GRCm39) missense probably benign 0.23
R1347:Fpr-rs6 UTSW 17 20,403,011 (GRCm39) missense probably benign 0.23
R1934:Fpr-rs6 UTSW 17 20,403,152 (GRCm39) missense probably benign 0.36
R1965:Fpr-rs6 UTSW 17 20,402,918 (GRCm39) missense probably damaging 0.98
R3690:Fpr-rs6 UTSW 17 20,403,137 (GRCm39) missense probably benign 0.02
R4564:Fpr-rs6 UTSW 17 20,403,168 (GRCm39) nonsense probably null
R4574:Fpr-rs6 UTSW 17 20,403,359 (GRCm39) start codon destroyed probably damaging 1.00
R5015:Fpr-rs6 UTSW 17 20,402,608 (GRCm39) missense probably damaging 1.00
R5599:Fpr-rs6 UTSW 17 20,402,375 (GRCm39) missense probably benign 0.05
R6737:Fpr-rs6 UTSW 17 20,403,339 (GRCm39) missense probably benign 0.08
R6786:Fpr-rs6 UTSW 17 20,403,100 (GRCm39) missense possibly damaging 0.95
R6908:Fpr-rs6 UTSW 17 20,402,701 (GRCm39) missense probably damaging 1.00
R7040:Fpr-rs6 UTSW 17 20,403,196 (GRCm39) missense probably damaging 1.00
R7462:Fpr-rs6 UTSW 17 20,402,485 (GRCm39) missense probably damaging 1.00
R7673:Fpr-rs6 UTSW 17 20,402,999 (GRCm39) missense probably benign 0.03
R7958:Fpr-rs6 UTSW 17 20,402,705 (GRCm39) missense probably damaging 0.98
R8103:Fpr-rs6 UTSW 17 20,402,839 (GRCm39) missense possibly damaging 0.69
R8772:Fpr-rs6 UTSW 17 20,402,495 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCCATCATGAGTGTCACATC -3'
(R):5'- GGCTTCAGCATACCAATGATCTTC -3'

Sequencing Primer
(F):5'- AGTGTCACATCCTATGGCTCAGAG -3'
(R):5'- TATGGACTCATGGCTGCCAAG -3'
Posted On 2015-04-29