Mutagenetix > Incidental Mutation

Incidental Mutation 'R7607:Plce1'

588408

Institutional Source

Beutler Lab

Gene Symbol

Plce1

Ensembl Gene

ENSMUSG00000024998

Gene Name

phospholipase C, epsilon 1

Synonyms

4933403A21Rik, PLCepsilon

MMRRC Submission

045677-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.463) question?

Stock #

R7607 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

38481109-38785030 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 38524752 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Glutamic Acid at position 165 (A165E)

Ref Sequence

ENSEMBL: ENSMUSP00000138330 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000169713] [ENSMUST00000182267] [ENSMUST00000182481]

AlphaFold

Q8K4S1

Predicted Effect

probably benign
Transcript: ENSMUST00000169713
AA Change: A165E

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

SMART Domains

Protein: ENSMUSP00000130604
Gene: ENSMUSG00000024998
AA Change: A165E

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	7.6e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1561	1575	N/A	INTRINSIC
SCOP:d1qasa3	1634	1662	1e-3	SMART
low complexity region	1666	1680	N/A	INTRINSIC
PLCYc	1710	1826	4.28e-46	SMART
C2	1850	1948	3.7e-10	SMART
PDB:2BYE\|A	1986	2094	6e-47	PDB
RA	2115	2218	1.12e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182267
AA Change: A165E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000138330
Gene: ENSMUSG00000024998
AA Change: A165E

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	5.9e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1552	1581	N/A	INTRINSIC
SCOP:d1qasa3	1648	1676	1e-3	SMART
low complexity region	1680	1694	N/A	INTRINSIC
PLCYc	1724	1840	4.28e-46	SMART
C2	1864	1962	3.7e-10	SMART
PDB:2BYE\|A	2000	2108	6e-47	PDB
RA	2129	2232	1.12e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182481
AA Change: A165E

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

SMART Domains

Protein: ENSMUSP00000138360
Gene: ENSMUSG00000024998
AA Change: A165E

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	8e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1561	1575	N/A	INTRINSIC
SCOP:d1qasa3	1634	1662	1e-3	SMART
low complexity region	1666	1680	N/A	INTRINSIC
PLCYc	1710	1826	4.28e-46	SMART
C2	1850	1948	3.7e-10	SMART
PDB:2BYE\|A	1986	2094	6e-47	PDB
RA	2115	2218	1.12e-2	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

99% (69/70)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]
PHENOTYPE: Homozygous mutation of this gene results in a congenital semilunar valvulogenesis defect which causes regurgitation and stenosis, and decreased incidence of induced skin tumors. Another mutant exhibits decreased cardiac contraction and increased hypertrophy in response to chronic stress. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610010K14Rik	A	T	11: 70,237,557 (GRCm38)	H30Q	probably damaging	Het
1700012P22Rik	T	A	4: 144,419,762 (GRCm38)	H107L	probably damaging	Het
A930009A15Rik	G	A	10: 115,581,989 (GRCm38)		probably null	Het
Abca7	T	C	10: 80,011,833 (GRCm38)	L1779P	probably damaging	Het
Aff1	G	A	5: 103,849,459 (GRCm38)	V1140I	possibly damaging	Het
Ano2	C	T	6: 125,712,419 (GRCm38)	A169V	probably damaging	Het
Atat1	T	C	17: 35,909,107 (GRCm38)	Y101C	possibly damaging	Het
Atp6v1c1	T	C	15: 38,683,011 (GRCm38)		probably null	Het
Atp7b	T	G	8: 22,011,506 (GRCm38)	K912T	probably damaging	Het
Ceacam14	T	C	7: 17,814,321 (GRCm38)	V112A	possibly damaging	Het
Cobll1	T	C	2: 65,095,857 (GRCm38)	N1119S	probably benign	Het
Csmd1	G	T	8: 15,918,331 (GRCm38)	Q3099K	possibly damaging	Het
Cyp3a25	A	G	5: 145,984,981 (GRCm38)	V381A	possibly damaging	Het
Dctn1	C	T	6: 83,195,069 (GRCm38)	R948*	probably null	Het
Dhrs3	A	G	4: 144,923,940 (GRCm38)	T219A	probably benign	Het
Epha7	C	T	4: 28,871,937 (GRCm38)	S422L	probably benign	Het
Esrp1	A	G	4: 11,384,449 (GRCm38)	V78A	probably damaging	Het
Evc2	A	G	5: 37,386,856 (GRCm38)	T650A	possibly damaging	Het
Exoc6b	T	A	6: 84,989,409 (GRCm38)	K194N	possibly damaging	Het
Fer1l6	G	A	15: 58,662,732 (GRCm38)	W1809*	probably null	Het
Frmd4a	T	A	2: 4,591,936 (GRCm38)	L156*	probably null	Het
Gk5	A	T	9: 96,153,210 (GRCm38)		probably null	Het
Gm3573	A	G	14: 42,189,750 (GRCm38)	F8L	probably benign	Het
Gm906	T	C	13: 50,250,260 (GRCm38)	E2G	possibly damaging	Het
Gm9767	G	A	10: 26,078,940 (GRCm38)	C130Y	unknown	Het
Grip2	T	C	6: 91,788,412 (GRCm38)	T30A	probably benign	Het
Gskip	C	A	12: 105,698,897 (GRCm38)	A65E	possibly damaging	Het
Gtf2e2	A	G	8: 33,776,465 (GRCm38)	R259G	probably benign	Het
Gucy1b2	T	A	14: 62,419,177 (GRCm38)	I244F	probably damaging	Het
Gxylt2	G	T	6: 100,798,190 (GRCm38)	V357L	possibly damaging	Het
Hivep3	CGG	CG	4: 120,097,911 (GRCm38)	1141	probably null	Het
Igdcc4	C	T	9: 65,133,758 (GRCm38)	P1024S	possibly damaging	Het
Ino80	A	T	2: 119,382,269 (GRCm38)		probably null	Het
Knl1	T	C	2: 119,095,133 (GRCm38)	F1881S	possibly damaging	Het
Mbd6	T	C	10: 127,285,230 (GRCm38)	E518G	unknown	Het
Mlh1	A	G	9: 111,229,890 (GRCm38)	S689P	probably damaging	Het
Mmrn2	T	C	14: 34,398,940 (GRCm38)	I589T	possibly damaging	Het
Mtmr12	C	T	15: 12,257,708 (GRCm38)	Q291*	probably null	Het
Mup8	T	A	4: 60,222,035 (GRCm38)	I33F	probably benign	Het
Mylk	C	T	16: 34,894,814 (GRCm38)	P504L	probably benign	Het
Ntrk3	C	T	7: 78,250,873 (GRCm38)	A573T	probably benign	Het
Obscn	G	T	11: 58,998,265 (GRCm38)	S7560R	unknown	Het
Olfr24	A	G	9: 18,754,882 (GRCm38)	F251S	possibly damaging	Het
Olfr617	A	C	7: 103,584,930 (GRCm38)	T303P	probably damaging	Het
Pde1c	T	C	6: 56,150,628 (GRCm38)	T391A	probably damaging	Het
Pla2g4d	T	A	2: 120,288,976 (GRCm38)	H19L	probably benign	Het
Polr1a	T	C	6: 71,913,021 (GRCm38)	S75P	probably benign	Het
Psg21	T	C	7: 18,654,783 (GRCm38)	E128G	probably benign	Het
Radil	A	T	5: 142,494,795 (GRCm38)	M635K	probably damaging	Het
Radil	A	G	5: 142,506,613 (GRCm38)	I420T	probably damaging	Het
Rnase11	G	A	14: 51,049,572 (GRCm38)	T175I	probably damaging	Het
Robo1	C	T	16: 72,563,738 (GRCm38)	P13S		Het
Slc18a2	C	A	19: 59,284,358 (GRCm38)	A364D	probably benign	Het
Snph	C	T	2: 151,594,586 (GRCm38)	D141N	probably damaging	Het
Snrnp70	T	C	7: 45,392,264 (GRCm38)	K70R	possibly damaging	Het
Snx33	T	C	9: 56,926,713 (GRCm38)	D24G	probably benign	Het
Spag6	T	A	2: 18,731,962 (GRCm38)	D165E	possibly damaging	Het
Spata31	T	G	13: 64,921,592 (GRCm38)	L518R	probably damaging	Het
Sspo	G	A	6: 48,489,727 (GRCm38)	V4059M	probably damaging	Het
St6galnac2	T	C	11: 116,679,979 (GRCm38)	Y261C	probably damaging	Het
Stoml1	A	G	9: 58,256,658 (GRCm38)	R87G	probably damaging	Het
Suv39h2	T	C	2: 3,474,829 (GRCm38)	T40A	unknown	Het
Terb2	G	T	2: 122,186,475 (GRCm38)	G26W	probably damaging	Het
Tmem62	T	C	2: 120,996,440 (GRCm38)	I406T	probably benign	Het
Tnfrsf11a	G	A	1: 105,844,732 (GRCm38)	V582I	probably benign	Het
Tpsg1	G	T	17: 25,373,210 (GRCm38)	G86V	probably damaging	Het
Unc13c	T	C	9: 73,669,535 (GRCm38)	D1480G	probably damaging	Het
Urb1	CACTTAC	CAC	16: 90,772,573 (GRCm38)		probably benign	Het
Vmn1r48	C	A	6: 90,035,980 (GRCm38)	V288L	probably benign	Het
Vmn2r13	A	G	5: 109,173,640 (GRCm38)	V397A	probably damaging	Het
Vmn2r98	A	G	17: 19,067,308 (GRCm38)	N468D	possibly damaging	Het
Zfhx2	G	T	14: 55,066,231 (GRCm38)	T1432K	possibly damaging	Het
Zswim5	T	A	4: 116,986,742 (GRCm38)	D992E	possibly damaging	Het

Other mutations in Plce1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Plce1	APN	19	38,745,788 (GRCm38)	missense	probably damaging	0.99
IGL00336:Plce1	APN	19	38,651,906 (GRCm38)	missense	probably damaging	1.00
IGL00430:Plce1	APN	19	38,725,017 (GRCm38)	missense	probably damaging	1.00
IGL00466:Plce1	APN	19	38,721,029 (GRCm38)	missense	probably damaging	0.99
IGL00477:Plce1	APN	19	38,525,132 (GRCm38)	missense	probably benign	0.39
IGL00839:Plce1	APN	19	38,698,562 (GRCm38)	missense	probably damaging	1.00
IGL01292:Plce1	APN	19	38,651,785 (GRCm38)	splice site	probably benign
IGL01665:Plce1	APN	19	38,524,887 (GRCm38)	missense	probably benign	0.01
IGL01826:Plce1	APN	19	38,739,238 (GRCm38)	splice site	probably benign
IGL01833:Plce1	APN	19	38,720,981 (GRCm38)	missense	probably damaging	1.00
IGL02201:Plce1	APN	19	38,769,446 (GRCm38)	splice site	probably benign
IGL02276:Plce1	APN	19	38,524,757 (GRCm38)	missense	probably benign	0.05
IGL02477:Plce1	APN	19	38,719,553 (GRCm38)	splice site	probably benign
IGL02746:Plce1	APN	19	38,698,472 (GRCm38)	missense	probably damaging	1.00
Angel_food	UTSW	19	38,727,013 (GRCm38)	splice site	probably benign
Heavenly	UTSW	19	38,777,989 (GRCm38)	missense	probably damaging	1.00
R0058:Plce1	UTSW	19	38,525,184 (GRCm38)	missense	possibly damaging	0.90
R0058:Plce1	UTSW	19	38,525,184 (GRCm38)	missense	possibly damaging	0.90
R0064:Plce1	UTSW	19	38,780,784 (GRCm38)	critical splice donor site	probably null
R0116:Plce1	UTSW	19	38,721,821 (GRCm38)	missense	probably benign
R0138:Plce1	UTSW	19	38,524,419 (GRCm38)	missense	possibly damaging	0.49
R0240:Plce1	UTSW	19	38,728,886 (GRCm38)	missense	probably damaging	0.99
R0240:Plce1	UTSW	19	38,728,886 (GRCm38)	missense	probably damaging	0.99
R0504:Plce1	UTSW	19	38,778,021 (GRCm38)	splice site	probably benign
R0506:Plce1	UTSW	19	38,760,138 (GRCm38)	missense	probably benign	0.04
R0578:Plce1	UTSW	19	38,777,939 (GRCm38)	missense	probably damaging	1.00
R0645:Plce1	UTSW	19	38,777,989 (GRCm38)	missense	probably damaging	1.00
R0730:Plce1	UTSW	19	38,716,691 (GRCm38)	missense	probably damaging	0.98
R0920:Plce1	UTSW	19	38,736,521 (GRCm38)	missense	probably damaging	1.00
R1223:Plce1	UTSW	19	38,767,226 (GRCm38)	missense	probably damaging	1.00
R1223:Plce1	UTSW	19	38,702,013 (GRCm38)	missense	probably damaging	1.00
R1484:Plce1	UTSW	19	38,705,339 (GRCm38)	nonsense	probably null
R1488:Plce1	UTSW	19	38,716,803 (GRCm38)	missense	possibly damaging	0.92
R1598:Plce1	UTSW	19	38,720,996 (GRCm38)	missense	probably damaging	1.00
R1624:Plce1	UTSW	19	38,724,775 (GRCm38)	missense	probably damaging	1.00
R1732:Plce1	UTSW	19	38,716,838 (GRCm38)	missense	possibly damaging	0.56
R1778:Plce1	UTSW	19	38,780,790 (GRCm38)	splice site	probably benign
R1797:Plce1	UTSW	19	38,758,948 (GRCm38)	critical splice donor site	probably null
R1872:Plce1	UTSW	19	38,760,077 (GRCm38)	missense	probably damaging	1.00
R1876:Plce1	UTSW	19	38,780,623 (GRCm38)	missense	probably damaging	1.00
R1991:Plce1	UTSW	19	38,777,924 (GRCm38)	missense	probably damaging	1.00
R2080:Plce1	UTSW	19	38,727,013 (GRCm38)	splice site	probably benign
R2103:Plce1	UTSW	19	38,777,924 (GRCm38)	missense	probably damaging	1.00
R2376:Plce1	UTSW	19	38,777,986 (GRCm38)	missense	probably benign	0.02
R2471:Plce1	UTSW	19	38,779,926 (GRCm38)	missense	probably damaging	1.00
R2511:Plce1	UTSW	19	38,760,054 (GRCm38)	missense	probably damaging	1.00
R2842:Plce1	UTSW	19	38,524,283 (GRCm38)	missense	probably damaging	1.00
R3037:Plce1	UTSW	19	38,777,884 (GRCm38)	missense	probably damaging	0.98
R3104:Plce1	UTSW	19	38,620,519 (GRCm38)	missense	probably benign	0.00
R3700:Plce1	UTSW	19	38,705,337 (GRCm38)	missense	probably damaging	1.00
R3750:Plce1	UTSW	19	38,777,899 (GRCm38)	missense	probably benign
R3753:Plce1	UTSW	19	38,651,834 (GRCm38)	missense	probably benign	0.09
R4027:Plce1	UTSW	19	38,524,265 (GRCm38)	missense	probably damaging	1.00
R4057:Plce1	UTSW	19	38,760,119 (GRCm38)	missense	probably damaging	1.00
R4376:Plce1	UTSW	19	38,705,447 (GRCm38)	critical splice donor site	probably null
R4433:Plce1	UTSW	19	38,767,301 (GRCm38)	missense	probably damaging	1.00
R4520:Plce1	UTSW	19	38,524,319 (GRCm38)	missense	possibly damaging	0.46
R4521:Plce1	UTSW	19	38,524,319 (GRCm38)	missense	possibly damaging	0.46
R4522:Plce1	UTSW	19	38,524,319 (GRCm38)	missense	possibly damaging	0.46
R4524:Plce1	UTSW	19	38,524,319 (GRCm38)	missense	possibly damaging	0.46
R4650:Plce1	UTSW	19	38,524,644 (GRCm38)	missense	probably benign	0.30
R4673:Plce1	UTSW	19	38,749,396 (GRCm38)	missense	possibly damaging	0.51
R4701:Plce1	UTSW	19	38,725,007 (GRCm38)	missense	probably benign	0.33
R4828:Plce1	UTSW	19	38,769,499 (GRCm38)	missense	probably damaging	1.00
R5103:Plce1	UTSW	19	38,767,215 (GRCm38)	missense	probably damaging	1.00
R5112:Plce1	UTSW	19	38,651,833 (GRCm38)	missense	probably benign	0.00
R5236:Plce1	UTSW	19	38,770,347 (GRCm38)	missense	probably benign	0.11
R5268:Plce1	UTSW	19	38,758,835 (GRCm38)	missense	possibly damaging	0.71
R5288:Plce1	UTSW	19	38,760,091 (GRCm38)	missense	probably damaging	1.00
R5384:Plce1	UTSW	19	38,760,091 (GRCm38)	missense	probably damaging	1.00
R5386:Plce1	UTSW	19	38,760,091 (GRCm38)	missense	probably damaging	1.00
R5448:Plce1	UTSW	19	38,779,917 (GRCm38)	missense	probably damaging	1.00
R5452:Plce1	UTSW	19	38,620,482 (GRCm38)	missense	probably benign	0.01
R6004:Plce1	UTSW	19	38,721,871 (GRCm38)	missense	probably damaging	1.00
R6062:Plce1	UTSW	19	38,524,751 (GRCm38)	missense	probably benign
R6147:Plce1	UTSW	19	38,702,037 (GRCm38)	missense	probably damaging	1.00
R6247:Plce1	UTSW	19	38,745,845 (GRCm38)	missense	probably damaging	1.00
R6278:Plce1	UTSW	19	38,725,051 (GRCm38)	splice site	probably null
R6306:Plce1	UTSW	19	38,769,465 (GRCm38)	missense	probably damaging	1.00
R6317:Plce1	UTSW	19	38,524,530 (GRCm38)	nonsense	probably null
R6437:Plce1	UTSW	19	38,525,132 (GRCm38)	missense	probably benign	0.39
R6522:Plce1	UTSW	19	38,748,521 (GRCm38)	splice site	probably null
R7034:Plce1	UTSW	19	38,739,357 (GRCm38)	missense	probably damaging	1.00
R7036:Plce1	UTSW	19	38,739,357 (GRCm38)	missense	probably damaging	1.00
R7037:Plce1	UTSW	19	38,702,017 (GRCm38)	missense	probably damaging	1.00
R7069:Plce1	UTSW	19	38,758,940 (GRCm38)	missense	probably damaging	1.00
R7180:Plce1	UTSW	19	38,779,785 (GRCm38)	missense	probably damaging	1.00
R7189:Plce1	UTSW	19	38,760,137 (GRCm38)	missense	probably damaging	0.97
R7227:Plce1	UTSW	19	38,726,902 (GRCm38)	missense	probably benign	0.00
R7253:Plce1	UTSW	19	38,698,508 (GRCm38)	missense	probably damaging	1.00
R7278:Plce1	UTSW	19	38,779,896 (GRCm38)	missense	possibly damaging	0.58
R7287:Plce1	UTSW	19	38,701,903 (GRCm38)	missense	probably benign	0.02
R7422:Plce1	UTSW	19	38,651,885 (GRCm38)	missense	probably damaging	1.00
R7557:Plce1	UTSW	19	38,765,404 (GRCm38)	missense	probably benign	0.30
R7615:Plce1	UTSW	19	38,524,665 (GRCm38)	missense	probably benign	0.18
R7653:Plce1	UTSW	19	38,749,319 (GRCm38)	missense	probably benign	0.20
R7685:Plce1	UTSW	19	38,748,433 (GRCm38)	missense	probably benign	0.00
R7716:Plce1	UTSW	19	38,716,851 (GRCm38)	missense	probably benign
R7744:Plce1	UTSW	19	38,620,455 (GRCm38)	missense	possibly damaging	0.93
R7790:Plce1	UTSW	19	38,780,696 (GRCm38)	missense	probably damaging	0.97
R7921:Plce1	UTSW	19	38,620,553 (GRCm38)	missense	probably benign	0.03
R8070:Plce1	UTSW	19	38,701,839 (GRCm38)	missense	probably damaging	0.99
R8087:Plce1	UTSW	19	38,736,521 (GRCm38)	missense	probably damaging	1.00
R8116:Plce1	UTSW	19	38,524,818 (GRCm38)	missense	probably benign	0.32
R8178:Plce1	UTSW	19	38,772,979 (GRCm38)	missense	possibly damaging	0.93
R8321:Plce1	UTSW	19	38,651,936 (GRCm38)	missense	probably benign	0.00
R8416:Plce1	UTSW	19	38,772,997 (GRCm38)	missense	possibly damaging	0.77
R8544:Plce1	UTSW	19	38,524,459 (GRCm38)	missense	probably benign	0.00
R8713:Plce1	UTSW	19	38,524,901 (GRCm38)	missense	probably benign	0.01
R8850:Plce1	UTSW	19	38,524,367 (GRCm38)	missense	probably benign
R9217:Plce1	UTSW	19	38,760,107 (GRCm38)	missense	probably damaging	1.00
R9231:Plce1	UTSW	19	38,716,596 (GRCm38)	missense	probably benign	0.13
R9232:Plce1	UTSW	19	38,716,979 (GRCm38)	missense	probably benign	0.16
R9332:Plce1	UTSW	19	38,737,933 (GRCm38)	missense	probably damaging	1.00
R9473:Plce1	UTSW	19	38,777,893 (GRCm38)	missense	possibly damaging	0.93
R9474:Plce1	UTSW	19	38,777,893 (GRCm38)	missense	possibly damaging	0.93
R9475:Plce1	UTSW	19	38,777,893 (GRCm38)	missense	possibly damaging	0.93
R9476:Plce1	UTSW	19	38,777,893 (GRCm38)	missense	possibly damaging	0.93
R9751:Plce1	UTSW	19	38,728,970 (GRCm38)	missense	probably damaging	1.00
R9780:Plce1	UTSW	19	38,620,690 (GRCm38)	missense	possibly damaging	0.94
R9781:Plce1	UTSW	19	38,525,210 (GRCm38)	missense	probably damaging	1.00
RF018:Plce1	UTSW	19	38,717,207 (GRCm38)	missense	probably damaging	0.99
X0022:Plce1	UTSW	19	38,726,999 (GRCm38)	missense	probably damaging	1.00
X0065:Plce1	UTSW	19	38,777,914 (GRCm38)	missense	possibly damaging	0.48
Z1176:Plce1	UTSW	19	38,769,460 (GRCm38)	missense	probably damaging	1.00
Z1176:Plce1	UTSW	19	38,724,980 (GRCm38)	nonsense	probably null
Z1176:Plce1	UTSW	19	38,701,894 (GRCm38)	missense	probably damaging	1.00
Z1177:Plce1	UTSW	19	38,651,842 (GRCm38)	missense	probably null	0.48

Predicted Primers

PCR Primer
(F):5'- ATGAACGGCAACAGTTTAGTG -3'
(R):5'- AACTCCACCAGTTTGCAAGC -3'

Sequencing Primer
(F):5'- GTTTAGTGCAAAGCCACCAG -3'
(R):5'- GTTTGCAAGCATACGCCATG -3'

Posted On

2019-10-24