Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01067:Fpr3'

53005

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fpr3

Ensembl Gene

ENSMUSG00000079700

Gene Name

formyl peptide receptor 3

Synonyms

Fprl1, LXA4-R, Lxa4r, Fpr-rs1

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL01067

Quality Score

Status

Chromosome

Chromosomal Location

18190720-18191939 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 18190828 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 33 (V33D)

Ref Sequence

ENSEMBL: ENSMUSP00000111227 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054871] [ENSMUST00000115565]

AlphaFold

O08790

Predicted Effect

probably benign
Transcript: ENSMUST00000054871
AA Change: V33D

PolyPhen 2 Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000093316
Gene: ENSMUSG00000079700
AA Change: V33D

Domain	Start	End	E-Value	Type
Pfam:7tm_1	43	302	2.2e-43	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000115565
AA Change: V33D

PolyPhen 2 Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000111227
Gene: ENSMUSG00000079700
AA Change: V33D

Domain	Start	End	E-Value	Type
Pfam:7tm_1	43	302	1.5e-36	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110038F14Rik	G	A	15: 76,834,475 (GRCm39)	V124I	probably damaging	Het
A330008L17Rik	T	C	8: 100,148,586 (GRCm39)		noncoding transcript	Het
Acp4	C	T	7: 43,902,876 (GRCm39)	V331I	probably benign	Het
Aen	G	A	7: 78,557,050 (GRCm39)	M299I	probably damaging	Het
Alg6	T	C	4: 99,629,807 (GRCm39)	V128A	probably benign	Het
Ank3	A	G	10: 69,686,026 (GRCm39)	K280E	probably damaging	Het
Bfar	T	C	16: 13,503,105 (GRCm39)	C36R	probably damaging	Het
Car14	A	G	3: 95,806,128 (GRCm39)	I311T	probably damaging	Het
Cd300c	T	C	11: 114,851,253 (GRCm39)		probably benign	Het
Cfap100	T	A	6: 90,383,096 (GRCm39)	E513V	probably damaging	Het
Clip1	C	A	5: 123,768,867 (GRCm39)	K612N	probably damaging	Het
Depdc5	A	G	5: 33,056,411 (GRCm39)		probably null	Het
Dock3	A	T	9: 106,959,572 (GRCm39)		probably null	Het
Dph6	A	T	2: 114,478,290 (GRCm39)	M17K	probably damaging	Het
Enkur	T	C	2: 21,194,042 (GRCm39)	Q177R	probably benign	Het
Faap100	T	C	11: 120,262,958 (GRCm39)	H800R	probably damaging	Het
Fastkd2	T	G	1: 63,776,930 (GRCm39)		probably benign	Het
Fcgr2b	A	T	1: 170,795,622 (GRCm39)	N102K	possibly damaging	Het
Fezf1	C	T	6: 23,247,842 (GRCm39)	V78I	possibly damaging	Het
Fmn2	A	T	1: 174,330,885 (GRCm39)	D425V	unknown	Het
Fnta	G	A	8: 26,497,229 (GRCm39)	Q207*	probably null	Het
Fshr	C	T	17: 89,292,821 (GRCm39)	C619Y	possibly damaging	Het
Gbp3	T	C	3: 142,272,358 (GRCm39)		probably null	Het
Gjb2	A	G	14: 57,337,629 (GRCm39)	V193A	possibly damaging	Het
Il4ra	A	G	7: 125,174,333 (GRCm39)	T292A	probably benign	Het
Lama5	A	G	2: 179,818,336 (GRCm39)		probably benign	Het
Marveld3	G	T	8: 110,688,596 (GRCm39)	D48E	possibly damaging	Het
Meox1	A	T	11: 101,784,599 (GRCm39)	I78N	probably benign	Het
Ncor1	A	T	11: 62,283,354 (GRCm39)	H444Q	probably damaging	Het
Ndst3	T	C	3: 123,340,466 (GRCm39)	Q784R	probably damaging	Het
Or10ag2	A	G	2: 87,248,714 (GRCm39)	I107M	probably benign	Het
Or4k44	T	A	2: 111,368,359 (GRCm39)	I92F	probably damaging	Het
Pld5	A	T	1: 176,102,445 (GRCm39)		probably benign	Het
Plk1	G	A	7: 121,768,148 (GRCm39)	R456H	probably damaging	Het
Polr2a	T	A	11: 69,638,840 (GRCm39)	I65F	possibly damaging	Het
Ptprd	T	A	4: 75,977,922 (GRCm39)	I196F	probably damaging	Het
Qsox2	T	C	2: 26,118,408 (GRCm39)	N121S	probably damaging	Het
Reln	A	G	5: 22,184,664 (GRCm39)	L1617S	probably damaging	Het
Rragc	T	C	4: 123,823,761 (GRCm39)	F345L	probably benign	Het
Sass6	A	T	3: 116,407,605 (GRCm39)	E240D	possibly damaging	Het
Shcbp1l	A	C	1: 153,311,770 (GRCm39)	S308R	possibly damaging	Het
Slc1a5	T	A	7: 16,520,804 (GRCm39)	C224*	probably null	Het
Slc27a5	T	C	7: 12,722,999 (GRCm39)	E567G	probably damaging	Het
Synj2	T	A	17: 6,088,201 (GRCm39)	N1417K	possibly damaging	Het
Tbc1d9	A	G	8: 83,960,791 (GRCm39)	T214A	probably damaging	Het
Tjp3	C	A	10: 81,109,699 (GRCm39)	V835L	probably benign	Het
Trpc4	C	A	3: 54,129,983 (GRCm39)	Q250K	probably benign	Het
Ttn	A	T	2: 76,575,506 (GRCm39)	I25129N	probably damaging	Het
Ube4a	T	A	9: 44,856,163 (GRCm39)	Y523F	probably damaging	Het
Zfp971	G	A	2: 177,665,175 (GRCm39)		probably null	Het

Other mutations in Fpr3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01520:Fpr3	APN	17	18,191,325 (GRCm39)	missense	possibly damaging	0.69
IGL02166:Fpr3	APN	17	18,190,726 (GRCm39)	utr 5 prime	probably benign
IGL02380:Fpr3	APN	17	18,191,254 (GRCm39)	missense	probably benign	0.00
IGL02587:Fpr3	APN	17	18,190,953 (GRCm39)	missense	probably benign	0.12
R1521:Fpr3	UTSW	17	18,191,277 (GRCm39)	missense	probably damaging	1.00
R1533:Fpr3	UTSW	17	18,190,922 (GRCm39)	nonsense	probably null
R1913:Fpr3	UTSW	17	18,191,670 (GRCm39)	missense	probably damaging	0.96
R2099:Fpr3	UTSW	17	18,191,443 (GRCm39)	missense	probably damaging	1.00
R2140:Fpr3	UTSW	17	18,190,879 (GRCm39)	missense	probably damaging	1.00
R2206:Fpr3	UTSW	17	18,190,908 (GRCm39)	missense	probably damaging	1.00
R2219:Fpr3	UTSW	17	18,191,644 (GRCm39)	missense	possibly damaging	0.93
R2224:Fpr3	UTSW	17	18,191,455 (GRCm39)	missense	probably damaging	1.00
R2244:Fpr3	UTSW	17	18,191,449 (GRCm39)	missense	probably benign	0.03
R2994:Fpr3	UTSW	17	18,191,130 (GRCm39)	nonsense	probably null
R5364:Fpr3	UTSW	17	18,190,806 (GRCm39)	missense	probably benign	0.00
R6179:Fpr3	UTSW	17	18,190,919 (GRCm39)	nonsense	probably null
R6781:Fpr3	UTSW	17	18,190,978 (GRCm39)	missense	probably benign	0.09
R6909:Fpr3	UTSW	17	18,191,429 (GRCm39)	missense	probably benign	0.00
R7565:Fpr3	UTSW	17	18,191,227 (GRCm39)	missense	probably damaging	1.00
R8008:Fpr3	UTSW	17	18,191,715 (GRCm39)	missense	probably benign	0.03
R8097:Fpr3	UTSW	17	18,191,054 (GRCm39)	missense	probably damaging	1.00
R8351:Fpr3	UTSW	17	18,191,436 (GRCm39)	missense	probably benign	0.27
R8732:Fpr3	UTSW	17	18,191,223 (GRCm39)	missense	possibly damaging	0.94
R8994:Fpr3	UTSW	17	18,191,341 (GRCm39)	missense	possibly damaging	0.92
R9076:Fpr3	UTSW	17	18,191,725 (GRCm39)	missense	probably benign
R9206:Fpr3	UTSW	17	18,191,131 (GRCm39)	missense	probably damaging	1.00
R9208:Fpr3	UTSW	17	18,191,131 (GRCm39)	missense	probably damaging	1.00
R9327:Fpr3	UTSW	17	18,191,713 (GRCm39)	missense	probably damaging	1.00
R9553:Fpr3	UTSW	17	18,191,612 (GRCm39)	missense	probably damaging	1.00
X0021:Fpr3	UTSW	17	18,191,500 (GRCm39)	missense	probably benign	0.06
Z1176:Fpr3	UTSW	17	18,191,255 (GRCm39)	missense	possibly damaging	0.55

Posted On

2013-06-21