Incidental Mutation 'IGL02166:Fpr3'
ID282730
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fpr3
Ensembl Gene ENSMUSG00000079700
Gene Nameformyl peptide receptor 3
SynonymsLXA4-R, Fpr-rs1, Lxa4r, Fprl1
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL02166
Quality Score
Status
Chromosome17
Chromosomal Location17887852-17971677 bp(+) (GRCm38)
Type of Mutationutr 5 prime
DNA Base Change (assembly) T to C at 17970464 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000111227 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054871] [ENSMUST00000115565]
Predicted Effect probably benign
Transcript: ENSMUST00000054871
SMART Domains Protein: ENSMUSP00000093316
Gene: ENSMUSG00000079700

DomainStartEndE-ValueType
Pfam:7tm_1 43 302 2.2e-43 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115565
SMART Domains Protein: ENSMUSP00000111227
Gene: ENSMUSG00000079700

DomainStartEndE-ValueType
Pfam:7tm_1 43 302 1.5e-36 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010111I01Rik A G 13: 63,015,453 H96R probably benign Het
Brd8 C T 18: 34,602,727 S899N probably damaging Het
Cdh8 T C 8: 99,190,451 D344G probably damaging Het
Cltc T C 11: 86,704,088 I1399V probably benign Het
Col4a1 A T 8: 11,244,509 probably benign Het
Crtc3 C T 7: 80,677,399 G60R probably damaging Het
Dscaml1 G A 9: 45,683,701 V701M probably damaging Het
Eif3b T A 5: 140,439,950 C632S possibly damaging Het
Ephb3 G A 16: 21,220,749 R417Q probably damaging Het
Hpdl A G 4: 116,820,952 V104A probably damaging Het
Ighv1-55 T C 12: 115,208,220 S76G probably benign Het
Ikbip T C 10: 91,095,790 S99P probably damaging Het
Lnpk T C 2: 74,529,717 E318G probably damaging Het
Lrrc66 G A 5: 73,607,291 T803M probably damaging Het
Narfl A G 17: 25,780,320 D236G possibly damaging Het
Nxf2 C A X: 134,957,129 W89L possibly damaging Het
Olfr1176 A T 2: 88,339,678 I38F probably damaging Het
Olfr1381 A G 11: 49,551,930 Y61C probably damaging Het
Olfr803 T A 10: 129,691,913 I43F probably benign Het
Osbp2 A T 11: 3,717,983 C5S probably damaging Het
Ovol2 T C 2: 144,305,730 N200S possibly damaging Het
Ppp4r1 A G 17: 65,813,492 D207G probably benign Het
Prdm11 C T 2: 93,012,863 V84M probably damaging Het
Rspo3 T A 10: 29,535,279 E17V possibly damaging Het
Scarf2 A G 16: 17,803,756 N357D probably damaging Het
Scn9a A T 2: 66,493,103 D1447E possibly damaging Het
Sdad1 G A 5: 92,291,762 T433I probably benign Het
Seh1l A G 18: 67,785,023 N149S probably damaging Het
Sigirr T C 7: 141,092,227 I268M probably benign Het
Slc35d2 A G 13: 64,098,348 F282S probably damaging Het
Slc4a1 A T 11: 102,354,333 M596K probably damaging Het
Spta1 G A 1: 174,190,231 E494K probably damaging Het
Stk32b C A 5: 37,499,030 probably benign Het
Tex13b T C X: 140,812,726 E122G probably damaging Het
Tmem35a A G X: 134,304,608 N91S probably damaging Het
Tmem67 A G 4: 12,047,313 V841A possibly damaging Het
Trdv2-1 A G 14: 53,946,611 D100G probably benign Het
Tshz3 T C 7: 36,768,921 S112P probably benign Het
Tssc4 T C 7: 143,070,201 M82T probably benign Het
Ttn A G 2: 76,732,379 S28744P probably damaging Het
Unc45b C T 11: 82,940,181 probably benign Het
Vim T C 2: 13,574,594 S55P probably damaging Het
Zmat5 T A 11: 4,737,363 Y139N possibly damaging Het
Zswim2 G A 2: 83,915,406 Q563* probably null Het
Other mutations in Fpr3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01067:Fpr3 APN 17 17970566 missense probably benign 0.17
IGL01520:Fpr3 APN 17 17971063 missense possibly damaging 0.69
IGL02380:Fpr3 APN 17 17970992 missense probably benign 0.00
IGL02587:Fpr3 APN 17 17970691 missense probably benign 0.12
R1521:Fpr3 UTSW 17 17971015 missense probably damaging 1.00
R1533:Fpr3 UTSW 17 17970660 nonsense probably null
R1913:Fpr3 UTSW 17 17971408 missense probably damaging 0.96
R2099:Fpr3 UTSW 17 17971181 missense probably damaging 1.00
R2140:Fpr3 UTSW 17 17970617 missense probably damaging 1.00
R2206:Fpr3 UTSW 17 17970646 missense probably damaging 1.00
R2219:Fpr3 UTSW 17 17971382 missense possibly damaging 0.93
R2224:Fpr3 UTSW 17 17971193 missense probably damaging 1.00
R2244:Fpr3 UTSW 17 17971187 missense probably benign 0.03
R2994:Fpr3 UTSW 17 17970868 nonsense probably null
R5364:Fpr3 UTSW 17 17970544 missense probably benign 0.00
R6179:Fpr3 UTSW 17 17970657 nonsense probably null
R6781:Fpr3 UTSW 17 17970716 missense probably benign 0.09
R6909:Fpr3 UTSW 17 17971167 missense probably benign 0.00
R7565:Fpr3 UTSW 17 17970965 missense probably damaging 1.00
R8008:Fpr3 UTSW 17 17971453 missense probably benign 0.03
X0021:Fpr3 UTSW 17 17971238 missense probably benign 0.06
Z1176:Fpr3 UTSW 17 17970993 missense possibly damaging 0.55
Posted On2015-04-16