Mutagenetix > Incidental Mutation

Incidental Mutation 'R4606:Pla2g4f'

345995

Institutional Source

Beutler Lab

Gene Symbol

Pla2g4f

Ensembl Gene

ENSMUSG00000046971

Gene Name

phospholipase A2, group IVF

Synonyms

4732472I07Rik, Pla2zeta

MMRRC Submission

041817-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R4606 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

120130438-120144646 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 120144467 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glutamine at position 24 (R24Q)

Ref Sequence

ENSEMBL: ENSMUSP00000062607 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028752] [ENSMUST00000054651] [ENSMUST00000102501]

AlphaFold

Q50L41

Predicted Effect

probably benign
Transcript: ENSMUST00000028752

SMART Domains

Protein: ENSMUSP00000028752
Gene: ENSMUSG00000027291

Domain	Start	End	E-Value	Type
Pfam:CNH	19	280	8.3e-53	PFAM
Pfam:Clathrin	410	536	3.9e-9	PFAM
Pfam:Vps39_1	449	551	1.7e-35	PFAM
Pfam:Clathrin	570	740	2.3e-8	PFAM
Pfam:Vps39_2	761	869	5.1e-36	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000054651
AA Change: R24Q

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000062607
Gene: ENSMUSG00000046971
AA Change: R24Q

Domain	Start	End	E-Value	Type
C2	45	144	7.51e-11	SMART
PLAc	285	797	1.6e-13	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000102501

SMART Domains

Protein: ENSMUSP00000099559
Gene: ENSMUSG00000027291

Domain	Start	End	E-Value	Type
Pfam:CNH	20	291	1.3e-32	PFAM
Pfam:Clathrin	421	547	2e-9	PFAM
Pfam:Vps39_1	460	562	6.7e-36	PFAM
Pfam:Clathrin	582	751	2.3e-8	PFAM
Pfam:Vps39_2	772	880	6.6e-36	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129857

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133260

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142183

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.0%

Validation Efficiency

96% (69/72)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700011L22Rik	A	T	8: 79,937,374 (GRCm39)	W178R	probably benign	Het
Abcb5	T	C	12: 118,896,345 (GRCm39)		probably null	Het
Akr1b1	C	A	6: 34,283,599 (GRCm39)		probably benign	Het
Arid1a	A	G	4: 133,414,634 (GRCm39)	F1199S	unknown	Het
Atp4b	A	G	8: 13,439,998 (GRCm39)	F116S	probably damaging	Het
Atp6v1b1	T	C	6: 83,729,443 (GRCm39)	S127P	probably damaging	Het
Blk	C	T	14: 63,611,652 (GRCm39)	V428I	probably benign	Het
Ccser1	T	C	6: 61,288,568 (GRCm39)	S244P	probably damaging	Het
Ceacam1	T	A	7: 25,173,951 (GRCm39)	I235F	probably damaging	Het
Cyp2g1	T	A	7: 26,513,579 (GRCm39)	Y173N	possibly damaging	Het
Ddr2	T	A	1: 169,829,421 (GRCm39)	I278F	probably benign	Het
Degs1	T	C	1: 182,104,388 (GRCm39)	D299G	probably damaging	Het
Dip2b	G	A	15: 100,113,210 (GRCm39)	V1542I	possibly damaging	Het
Dmxl1	T	A	18: 50,095,248 (GRCm39)	S2942R	probably damaging	Het
Dpf1	T	A	7: 29,016,015 (GRCm39)		probably benign	Het
Ephb6	A	G	6: 41,593,508 (GRCm39)	Y518C	probably benign	Het
Eps15l1	A	T	8: 73,127,760 (GRCm39)	F606I	possibly damaging	Het
Extl1	A	G	4: 134,098,690 (GRCm39)	S114P	probably damaging	Het
Extl1	A	C	4: 134,098,691 (GRCm39)	D113E	probably benign	Het
Fat1	T	C	8: 45,403,720 (GRCm39)	V157A	possibly damaging	Het
Fcho1	A	T	8: 72,165,124 (GRCm39)	D444E	probably benign	Het
Fgd3	T	A	13: 49,450,036 (GRCm39)	D71V	probably damaging	Het
Fgd5	T	A	6: 91,965,190 (GRCm39)	D316E	possibly damaging	Het
Gys2	A	T	6: 142,400,210 (GRCm39)	F334I	possibly damaging	Het
Ik	G	T	18: 36,886,608 (GRCm39)	R360L	possibly damaging	Het
Kazn	A	C	4: 141,845,599 (GRCm39)		probably null	Het
Kmt2d	A	T	15: 98,737,597 (GRCm39)		probably benign	Het
Krr1	T	C	10: 111,811,582 (GRCm39)		probably benign	Het
Krt87	C	T	15: 101,384,930 (GRCm39)	E389K	probably benign	Het
Lrrc4c	T	C	2: 97,460,658 (GRCm39)	V428A	probably benign	Het
Lvrn	C	A	18: 46,997,832 (GRCm39)	T260K	possibly damaging	Het
Mcc	C	T	18: 44,601,488 (GRCm39)	E614K	probably damaging	Het
Msrb3	A	T	10: 120,685,902 (GRCm39)	V81D	probably damaging	Het
Muc19	C	T	15: 91,832,268 (GRCm39)		noncoding transcript	Het
Myadm	T	A	7: 3,345,916 (GRCm39)	L226*	probably null	Het
Myof	C	T	19: 37,955,547 (GRCm39)	V526M	probably damaging	Het
Nckap5l	A	G	15: 99,327,204 (GRCm39)		probably benign	Het
Or1r1	A	G	11: 73,874,718 (GRCm39)	S239P	probably damaging	Het
Or4b1	G	T	2: 89,979,160 (GRCm39)		probably benign	Het
Or4c35	C	A	2: 89,808,350 (GRCm39)	A76D	possibly damaging	Het
Or9g10	T	A	2: 85,584,284 (GRCm39)		probably benign	Het
Pars2	T	C	4: 106,511,247 (GRCm39)	V307A	probably benign	Het
Pcdhb1	T	G	18: 37,398,581 (GRCm39)	Y177*	probably null	Het
Pcdhb4	T	A	18: 37,441,705 (GRCm39)	D338E	probably damaging	Het
Pik3r2	G	A	8: 71,224,780 (GRCm39)	R199*	probably null	Het
Pnma2	T	C	14: 67,153,681 (GRCm39)	I35T	probably benign	Het
Podn	C	A	4: 107,875,064 (GRCm39)	A568S	probably benign	Het
Pou3f1	A	T	4: 124,552,629 (GRCm39)	E377V	probably damaging	Het
Ppfia1	T	C	7: 144,038,929 (GRCm39)	D494G	probably damaging	Het
Pramel34	A	T	5: 93,784,461 (GRCm39)	D137E	probably damaging	Het
Ptpn9	A	T	9: 56,929,495 (GRCm39)	T71S	possibly damaging	Het
Ptprz1	C	T	6: 23,001,486 (GRCm39)	P1192L	possibly damaging	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rnf217	T	A	10: 31,393,472 (GRCm39)	K370*	probably null	Het
Rpap2	G	A	5: 107,749,661 (GRCm39)	V62I	possibly damaging	Het
Scaper	A	T	9: 55,563,187 (GRCm39)		probably null	Het
Sos2	T	C	12: 69,661,380 (GRCm39)		probably benign	Het
Sptbn5	C	T	2: 119,897,927 (GRCm39)		probably null	Het
Sumo1	A	G	1: 59,683,668 (GRCm39)		probably benign	Het
Syne2	C	A	12: 76,036,027 (GRCm39)	N3771K	probably damaging	Het
Tbx18	T	C	9: 87,612,822 (GRCm39)	I26V	possibly damaging	Het
Trpm3	T	A	19: 22,955,988 (GRCm39)	M1140K	probably benign	Het
Usp29	G	A	7: 6,966,356 (GRCm39)		probably null	Het
Wdr7	C	T	18: 63,913,016 (GRCm39)	Q946*	probably null	Het
Ythdf1	T	C	2: 180,553,975 (GRCm39)	D46G	probably damaging	Het
Zfp217	T	C	2: 169,961,670 (GRCm39)	N219S	possibly damaging	Het
Zkscan3	A	G	13: 21,577,953 (GRCm39)	I256T	probably benign	Het

Other mutations in Pla2g4f

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00539:Pla2g4f	APN	2	120,133,219 (GRCm39)	missense	possibly damaging	0.53
IGL01652:Pla2g4f	APN	2	120,132,716 (GRCm39)	missense	possibly damaging	0.86
IGL02792:Pla2g4f	APN	2	120,133,850 (GRCm39)	missense	probably damaging	1.00
R0625:Pla2g4f	UTSW	2	120,135,522 (GRCm39)	missense	probably damaging	1.00
R1760:Pla2g4f	UTSW	2	120,144,547 (GRCm39)	unclassified	probably benign
R1799:Pla2g4f	UTSW	2	120,141,549 (GRCm39)	missense	possibly damaging	0.49
R2212:Pla2g4f	UTSW	2	120,133,587 (GRCm39)	missense	probably benign
R2351:Pla2g4f	UTSW	2	120,130,923 (GRCm39)	missense	probably benign	0.01
R3412:Pla2g4f	UTSW	2	120,133,587 (GRCm39)	missense	probably benign
R3414:Pla2g4f	UTSW	2	120,133,587 (GRCm39)	missense	probably benign
R3906:Pla2g4f	UTSW	2	120,130,980 (GRCm39)	missense	probably benign	0.28
R4084:Pla2g4f	UTSW	2	120,142,806 (GRCm39)	missense	probably benign	0.36
R4477:Pla2g4f	UTSW	2	120,134,153 (GRCm39)	missense	probably damaging	1.00
R4529:Pla2g4f	UTSW	2	120,131,100 (GRCm39)	missense	probably damaging	0.99
R4685:Pla2g4f	UTSW	2	120,135,496 (GRCm39)	missense	probably damaging	1.00
R4728:Pla2g4f	UTSW	2	120,131,402 (GRCm39)	missense	probably benign	0.19
R4782:Pla2g4f	UTSW	2	120,133,757 (GRCm39)	missense	probably damaging	1.00
R4957:Pla2g4f	UTSW	2	120,130,980 (GRCm39)	missense	probably benign	0.28
R5781:Pla2g4f	UTSW	2	120,135,504 (GRCm39)	missense	probably damaging	0.97
R6158:Pla2g4f	UTSW	2	120,131,552 (GRCm39)	missense	probably benign	0.21
R6232:Pla2g4f	UTSW	2	120,132,702 (GRCm39)	missense	possibly damaging	0.63
R6629:Pla2g4f	UTSW	2	120,138,723 (GRCm39)	missense	probably damaging	1.00
R6894:Pla2g4f	UTSW	2	120,134,077 (GRCm39)	missense	probably benign	0.44
R6939:Pla2g4f	UTSW	2	120,137,782 (GRCm39)	missense	probably damaging	1.00
R7131:Pla2g4f	UTSW	2	120,135,035 (GRCm39)	missense	probably null	0.01
R7221:Pla2g4f	UTSW	2	120,131,476 (GRCm39)	missense	probably benign	0.06
R7421:Pla2g4f	UTSW	2	120,137,737 (GRCm39)	missense	probably benign	0.07
R7767:Pla2g4f	UTSW	2	120,135,490 (GRCm39)	missense	possibly damaging	0.87
R8466:Pla2g4f	UTSW	2	120,130,963 (GRCm39)	missense	probably damaging	1.00
R9389:Pla2g4f	UTSW	2	120,132,781 (GRCm39)	missense	probably damaging	1.00
R9425:Pla2g4f	UTSW	2	120,133,264 (GRCm39)	missense	possibly damaging	0.75
R9500:Pla2g4f	UTSW	2	120,142,713 (GRCm39)	critical splice acceptor site	probably null
R9657:Pla2g4f	UTSW	2	120,135,138 (GRCm39)	missense	probably benign
R9714:Pla2g4f	UTSW	2	120,142,900 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CTAGTGCATTCCTGGCAAACC -3'
(R):5'- TTGTCAGACCTGAGCGACAG -3'

Sequencing Primer
(F):5'- ACAGGCAATGGTCTCAGGC -3'
(R):5'- CCTGAGCGACAGTGAATATAGCC -3'

Posted On

2015-09-25