Mutagenetix > Incidental Mutation

Incidental Mutation 'R7658:Peg3'

591348

Institutional Source

Beutler Lab

Gene Symbol

Peg3

Ensembl Gene

ENSMUSG00000002265

Gene Name

paternally expressed 3

Synonyms

Zfp102, Gcap4, End4, Pw1

MMRRC Submission

045703-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7658 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

6706891-6733430 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 6712609 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 871 (I871N)

Ref Sequence

ENSEMBL: ENSMUSP00000050750 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051209] [ENSMUST00000143703] [ENSMUST00000150182]

AlphaFold

Q3URU2

Predicted Effect

probably damaging
Transcript: ENSMUST00000051209
AA Change: I871N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000050750
Gene: ENSMUSG00000002265
AA Change: I871N

Domain	Start	End	E-Value	Type
low complexity region	6	19	N/A	INTRINSIC
low complexity region	213	221	N/A	INTRINSIC
ZnF_C2H2	325	347	7.26e-3	SMART
ZnF_C2H2	378	400	6.88e-4	SMART
ZnF_C2H2	436	458	2.95e-3	SMART
low complexity region	464	496	N/A	INTRINSIC
ZnF_C2H2	520	542	5.99e-4	SMART
low complexity region	691	698	N/A	INTRINSIC
ZnF_C2H2	850	872	2.99e-4	SMART
ZnF_C2H2	1091	1113	2.05e-2	SMART
ZnF_C2H2	1147	1169	1.04e-3	SMART
ZnF_C2H2	1209	1231	1.38e-3	SMART
ZnF_C2H2	1266	1289	1.89e-1	SMART
ZnF_C2H2	1317	1339	1.57e2	SMART
low complexity region	1373	1419	N/A	INTRINSIC
low complexity region	1440	1486	N/A	INTRINSIC
ZnF_C2H2	1488	1510	2.2e-2	SMART
ZnF_C2H2	1547	1569	1.38e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000143703

SMART Domains

Protein: ENSMUSP00000122423
Gene: ENSMUSG00000002265

Domain	Start	End	E-Value	Type
low complexity region	6	19	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000150182

SMART Domains

Protein: ENSMUSP00000116161
Gene: ENSMUSG00000002265

Domain	Start	End	E-Value	Type
low complexity region	6	19	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] In human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5' exons and a common promoter and both genes are paternally expressed (PMID:15203203). Alternative splicing events connect their shared 5' exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. In contrast, in other mammals ZIM2 does not undergo imprinting and, in mouse, cow, and likely other mammals as well, the ZIM2 and PEG3 genes do not share exons. Human PEG3 protein belongs to the Kruppel C2H2-type zinc finger protein family. PEG3 may play a role in cell proliferation and p53-mediated apoptosis. PEG3 has also shown tumor suppressor activity and tumorigenesis in glioma and ovarian cells. Alternative splicing of this PEG3 gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Sep 2009]
PHENOTYPE: Heterozygous mutant females exhibit growth retardation, impaired maternal behavior and diminished milk ejection, and fewer oxytocin neurons. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted, knock-out(1) Gene trapped(3)

Other mutations in this stock

Total: 95 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110025L11Rik	G	T	16: 88,860,618 (GRCm39)	S72Y	unknown	Het
Abca8b	T	A	11: 109,826,543 (GRCm39)	K1568N	probably benign	Het
Adcy6	T	A	15: 98,493,948 (GRCm39)	Y865F	probably benign	Het
Adgrf3	A	T	5: 30,402,204 (GRCm39)	V608D	probably benign	Het
Agbl1	G	T	7: 76,416,117 (GRCm39)	A965S	unknown	Het
Agbl3	C	T	6: 34,809,443 (GRCm39)	P690L	probably benign	Het
Akap9	C	G	5: 4,018,745 (GRCm39)	H1109D	probably benign	Het
Amt	A	C	9: 108,174,430 (GRCm39)	H65P	probably damaging	Het
Ankrd11	T	A	8: 123,620,403 (GRCm39)	T1150S	probably benign	Het
Arhgap15	A	C	2: 44,032,280 (GRCm39)	H288P	probably benign	Het
Arhgap39	A	T	15: 76,621,617 (GRCm39)	M328K	probably benign	Het
Arhgef12	T	C	9: 42,903,832 (GRCm39)	K743R	probably damaging	Het
Atg2a	T	G	19: 6,301,293 (GRCm39)	V789G	probably damaging	Het
Ccdc54	T	C	16: 50,410,844 (GRCm39)	T141A	probably benign	Het
Ccng2	C	G	5: 93,421,202 (GRCm39)	S237R	probably benign	Het
Cdh5	T	C	8: 104,856,033 (GRCm39)		probably null	Het
Cdkl3	T	C	11: 51,918,009 (GRCm39)	V404A	not run	Het
Chrm2	A	T	6: 36,500,184 (GRCm39)	I14F	probably benign	Het
Cnbp	T	C	6: 87,822,258 (GRCm39)	K89E	possibly damaging	Het
Cntn6	T	A	6: 104,627,444 (GRCm39)	D92E	probably benign	Het
Col15a1	T	C	4: 47,245,591 (GRCm39)	F114S	possibly damaging	Het
Csrnp1	A	G	9: 119,801,469 (GRCm39)	F530S	probably benign	Het
Dcun1d3	C	T	7: 119,456,891 (GRCm39)	V274M	probably damaging	Het
Dph2	T	A	4: 117,747,478 (GRCm39)	H302L	possibly damaging	Het
Fam162a	A	T	16: 35,866,770 (GRCm39)	Y118*	probably null	Het
Fam186a	A	G	15: 99,837,725 (GRCm39)	Y2840H	unknown	Het
Fto	A	G	8: 92,392,950 (GRCm39)	K466E	probably benign	Het
Gal	T	A	19: 3,463,309 (GRCm39)	Y41F	probably damaging	Het
Gigyf2	A	T	1: 87,346,860 (GRCm39)	L620F	unknown	Het
Git2	C	T	5: 114,904,550 (GRCm39)	R123H	probably damaging	Het
Glud1	A	T	14: 34,033,114 (GRCm39)	E87V	probably benign	Het
Gm21190	T	G	5: 15,732,923 (GRCm39)	E94A	possibly damaging	Het
Gm5592	T	C	7: 40,938,134 (GRCm39)	V472A	probably benign	Het
Gpc5	T	A	14: 115,665,620 (GRCm39)	N481K	possibly damaging	Het
Gpn2	A	G	4: 133,318,687 (GRCm39)	E304G	probably benign	Het
Gsdmc2	T	C	15: 63,696,903 (GRCm39)	T423A	probably damaging	Het
Gucy2e	G	A	11: 69,117,055 (GRCm39)	Q789*	probably null	Het
Gxylt2	T	A	6: 100,760,104 (GRCm39)	V213E	probably damaging	Het
Ighv1-75	G	A	12: 115,797,731 (GRCm39)	L64F	possibly damaging	Het
Il17re	T	C	6: 113,435,943 (GRCm39)	C30R	probably benign	Het
Il7	G	T	3: 7,669,142 (GRCm39)	D31E	probably benign	Het
Ints4	T	C	7: 97,178,460 (GRCm39)	Y687H	possibly damaging	Het
Kdelr1	T	G	7: 45,532,401 (GRCm39)	V202G	probably benign	Het
Khnyn	C	A	14: 56,124,596 (GRCm39)	Y283*	probably null	Het
Klf11	T	C	12: 24,703,670 (GRCm39)	V52A	probably damaging	Het
Klhl7	A	G	5: 24,346,284 (GRCm39)	N310S	probably benign	Het
Krt27	A	T	11: 99,240,312 (GRCm39)	L202Q	possibly damaging	Het
Lce1d	A	G	3: 92,593,354 (GRCm39)	C20R	unknown	Het
Lim2	A	T	7: 43,083,054 (GRCm39)	I80F	possibly damaging	Het
Lrrk2	T	A	15: 91,584,561 (GRCm39)	F326Y	possibly damaging	Het
Lyst	A	T	13: 13,905,061 (GRCm39)	Y3246F	possibly damaging	Het
Mafb	T	A	2: 160,208,355 (GRCm39)	H81L	possibly damaging	Het
Mfsd5	G	A	15: 102,189,312 (GRCm39)	R228H	probably benign	Het
Mmp1b	A	T	9: 7,386,675 (GRCm39)	F150I	possibly damaging	Het
Mthfd1	T	A	12: 76,317,209 (GRCm39)	L20Q	probably damaging	Het
Mxra8	A	G	4: 155,927,420 (GRCm39)	T402A	probably benign	Het
Ndc80	A	T	17: 71,815,658 (GRCm39)	L376M	probably damaging	Het
Nsd1	A	T	13: 55,425,452 (GRCm39)	R1536S	probably damaging	Het
Nup210l	C	A	3: 90,119,300 (GRCm39)	H1874Q	probably benign	Het
Nyap1	T	C	5: 137,731,236 (GRCm39)	H776R	probably benign	Het
Patj	C	A	4: 98,576,416 (GRCm39)	H1773Q	probably damaging	Het
Pax8	T	A	2: 24,326,523 (GRCm39)	T280S	probably benign	Het
Pcdhb19	A	G	18: 37,632,034 (GRCm39)	T610A	probably damaging	Het
Pde2a	A	G	7: 101,160,788 (GRCm39)	D919G	possibly damaging	Het
Pdk2	T	A	11: 94,919,791 (GRCm39)	Y240F	probably damaging	Het
Pex1	A	T	5: 3,646,244 (GRCm39)		probably benign	Het
Pgm2l1	C	T	7: 99,899,535 (GRCm39)	R50W	probably damaging	Het
Phkg1	T	A	5: 129,894,764 (GRCm39)	K262N	probably damaging	Het
Pik3r4	A	G	9: 105,521,710 (GRCm39)	E92G	probably damaging	Het
Prmt6	A	T	3: 110,157,701 (GRCm39)	V196E	possibly damaging	Het
Ptprn2	T	G	12: 116,685,739 (GRCm39)	M66R	probably benign	Het
Rai14	C	T	15: 10,593,189 (GRCm39)	G152R	probably damaging	Het
Recql5	A	T	11: 115,814,102 (GRCm39)	S348T	probably damaging	Het
Rfk	T	G	19: 17,376,046 (GRCm39)		probably null	Het
Ro60	T	C	1: 143,646,611 (GRCm39)	T45A	probably damaging	Het
Selenbp1	A	T	3: 94,851,413 (GRCm39)	M389L	probably benign	Het
Sipa1l2	G	A	8: 126,219,029 (GRCm39)	R103C	probably benign	Het
Slc10a6	T	A	5: 103,777,056 (GRCm39)	S15C	probably damaging	Het
Slc12a2	G	T	18: 58,065,596 (GRCm39)	V944L	probably benign	Het
Slc16a11	T	A	11: 70,106,143 (GRCm39)	L127Q	possibly damaging	Het
Spef1l	T	C	7: 139,556,531 (GRCm39)	N152S	probably benign	Het
St6gal1	A	G	16: 23,174,978 (GRCm39)	Y272C	probably damaging	Het
Stab2	C	A	10: 86,816,999 (GRCm39)	V133F	probably benign	Het
Stradb	G	A	1: 59,031,885 (GRCm39)	V266I	probably damaging	Het
Tmem150b	A	G	7: 4,723,758 (GRCm39)	W140R	probably benign	Het
Tnnt3	A	T	7: 142,065,833 (GRCm39)	K157*	probably null	Het
Ttn	T	G	2: 76,554,113 (GRCm39)	K30863N	probably damaging	Het
Vldlr	G	A	19: 27,220,536 (GRCm39)	R592H	probably benign	Het
Vmn1r12	A	T	6: 57,135,883 (GRCm39)		probably benign	Het
Vmn2r63	A	C	7: 42,574,693 (GRCm39)	S519R	probably damaging	Het
Zbtb22	G	C	17: 34,137,471 (GRCm39)	E539Q	probably damaging	Het
Zbtb44	G	A	9: 30,965,375 (GRCm39)	A262T	probably benign	Het
Zfp280d	A	T	9: 72,231,354 (GRCm39)	N455I	probably damaging	Het
Zfp287	T	C	11: 62,616,089 (GRCm39)	N201D	probably damaging	Het
Zfp988	T	C	4: 147,416,751 (GRCm39)	L395P	probably damaging	Het

Other mutations in Peg3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00158:Peg3	APN	7	6,713,273 (GRCm39)	missense	probably benign	0.09
IGL01410:Peg3	APN	7	6,710,624 (GRCm39)	missense	probably benign	0.04
IGL01415:Peg3	APN	7	6,714,652 (GRCm39)	missense	probably damaging	0.99
IGL02073:Peg3	APN	7	6,714,001 (GRCm39)	missense	probably damaging	1.00
IGL02193:Peg3	APN	7	6,714,927 (GRCm39)	missense	probably damaging	1.00
IGL02212:Peg3	APN	7	6,714,415 (GRCm39)	missense	probably benign	0.41
IGL02215:Peg3	APN	7	6,712,010 (GRCm39)	missense	probably benign	0.00
IGL02407:Peg3	APN	7	6,710,635 (GRCm39)	missense	probably damaging	0.99
IGL02586:Peg3	APN	7	6,713,068 (GRCm39)	missense	probably benign
IGL02673:Peg3	APN	7	6,713,413 (GRCm39)	missense	probably damaging	1.00
IGL02935:Peg3	APN	7	6,714,128 (GRCm39)	missense	probably damaging	1.00
IGL03277:Peg3	APN	7	6,714,673 (GRCm39)	missense	probably damaging	1.00
IGL03330:Peg3	APN	7	6,713,412 (GRCm39)	missense	probably damaging	1.00
IGL03393:Peg3	APN	7	6,710,648 (GRCm39)	missense	probably damaging	0.99
R0049:Peg3	UTSW	7	6,714,672 (GRCm39)	missense	possibly damaging	0.85
R0049:Peg3	UTSW	7	6,714,672 (GRCm39)	missense	possibly damaging	0.85
R0518:Peg3	UTSW	7	6,714,427 (GRCm39)	missense	probably damaging	1.00
R0521:Peg3	UTSW	7	6,714,427 (GRCm39)	missense	probably damaging	1.00
R1477:Peg3	UTSW	7	6,719,141 (GRCm39)	missense	probably damaging	1.00
R1716:Peg3	UTSW	7	6,710,780 (GRCm39)	missense	possibly damaging	0.93
R1721:Peg3	UTSW	7	6,712,900 (GRCm39)	missense	possibly damaging	0.92
R1732:Peg3	UTSW	7	6,712,084 (GRCm39)	missense	possibly damaging	0.72
R2051:Peg3	UTSW	7	6,715,720 (GRCm39)	missense	probably damaging	0.96
R2288:Peg3	UTSW	7	6,712,114 (GRCm39)	missense	probably damaging	0.96
R3606:Peg3	UTSW	7	6,711,508 (GRCm39)	missense	probably damaging	1.00
R5075:Peg3	UTSW	7	6,711,419 (GRCm39)	missense	probably damaging	1.00
R5076:Peg3	UTSW	7	6,711,419 (GRCm39)	missense	probably damaging	1.00
R5084:Peg3	UTSW	7	6,710,848 (GRCm39)	missense	probably damaging	1.00
R5097:Peg3	UTSW	7	6,713,026 (GRCm39)	missense	probably damaging	0.99
R5121:Peg3	UTSW	7	6,713,288 (GRCm39)	missense	probably benign	0.20
R5141:Peg3	UTSW	7	6,712,381 (GRCm39)	missense	probably benign	0.03
R5292:Peg3	UTSW	7	6,711,259 (GRCm39)	missense	probably damaging	1.00
R5294:Peg3	UTSW	7	6,720,848 (GRCm39)	missense	possibly damaging	0.88
R5342:Peg3	UTSW	7	6,712,969 (GRCm39)	missense	probably damaging	1.00
R5415:Peg3	UTSW	7	6,711,628 (GRCm39)	missense	probably benign
R5906:Peg3	UTSW	7	6,720,854 (GRCm39)	missense	probably damaging	0.99
R6056:Peg3	UTSW	7	6,712,570 (GRCm39)	missense	probably damaging	1.00
R6259:Peg3	UTSW	7	6,712,810 (GRCm39)	missense	probably damaging	0.99
R6529:Peg3	UTSW	7	6,711,071 (GRCm39)	missense	probably damaging	1.00
R6631:Peg3	UTSW	7	6,712,069 (GRCm39)	missense	possibly damaging	0.72
R6855:Peg3	UTSW	7	6,711,797 (GRCm39)	missense	probably benign	0.13
R6861:Peg3	UTSW	7	6,714,385 (GRCm39)	nonsense	probably null
R6864:Peg3	UTSW	7	6,715,761 (GRCm39)	missense	probably damaging	1.00
R6892:Peg3	UTSW	7	6,711,898 (GRCm39)	missense	possibly damaging	0.58
R7018:Peg3	UTSW	7	6,711,838 (GRCm39)	missense	possibly damaging	0.72
R7039:Peg3	UTSW	7	6,720,858 (GRCm39)	missense	probably damaging	0.99
R7066:Peg3	UTSW	7	6,711,856 (GRCm39)	missense	probably damaging	1.00
R7117:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
R7133:Peg3	UTSW	7	6,711,944 (GRCm39)	missense	probably damaging	1.00
R7493:Peg3	UTSW	7	6,712,723 (GRCm39)	missense	probably damaging	1.00
R7539:Peg3	UTSW	7	6,711,167 (GRCm39)	missense	probably benign	0.00
R7642:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
R7646:Peg3	UTSW	7	6,712,221 (GRCm39)	missense	probably benign
R7846:Peg3	UTSW	7	6,713,650 (GRCm39)	missense	probably damaging	1.00
R7853:Peg3	UTSW	7	6,711,839 (GRCm39)	missense	possibly damaging	0.72
R7903:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
R7913:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
R7948:Peg3	UTSW	7	6,711,781 (GRCm39)	missense	probably damaging	1.00
R8219:Peg3	UTSW	7	6,711,364 (GRCm39)	missense	probably benign	0.00
R8385:Peg3	UTSW	7	6,711,082 (GRCm39)	missense	probably damaging	1.00
R8672:Peg3	UTSW	7	6,711,523 (GRCm39)	missense	possibly damaging	0.62
R9133:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
R9209:Peg3	UTSW	7	6,711,226 (GRCm39)	missense	possibly damaging	0.48
R9457:Peg3	UTSW	7	6,710,998 (GRCm39)	missense	probably damaging	0.99
R9518:Peg3	UTSW	7	6,714,280 (GRCm39)	missense	probably benign	0.00
R9519:Peg3	UTSW	7	6,714,394 (GRCm39)	missense	probably benign	0.00
R9599:Peg3	UTSW	7	6,714,723 (GRCm39)	missense	probably damaging	0.97
RF039:Peg3	UTSW	7	6,712,167 (GRCm39)	unclassified	probably benign
YA93:Peg3	UTSW	7	6,714,646 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGCTCCTCGGCATTAAATGTC -3'
(R):5'- TTCGTGAACACCAGAAAGCTC -3'

Sequencing Primer
(F):5'- CGGCATTAAATGTCTCTTGGGCATAG -3'
(R):5'- CTCGTGCCAAAAAGAAGTACATTG -3'

Posted On

2019-11-12