Mutagenetix > Incidental Mutation

Incidental Mutation 'R6276:Peg10'

507633

Institutional Source

Beutler Lab

Gene Symbol

Peg10

Ensembl Gene

ENSMUSG00000092035

Gene Name

paternally expressed 10

Synonyms

HB-1, MyEF-3, Mart2, Mar2, MyEF-3 like, MEF3L, Edr

MMRRC Submission

044446-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6276 (G1)

Quality Score

149.467

Status

Validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm38)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

GAT to GATCAT at 4756449 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000135076 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166678] [ENSMUST00000176204] [ENSMUST00000176551]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000166678

SMART Domains

Protein: ENSMUSP00000127306
Gene: ENSMUSG00000092035

Domain	Start	End	E-Value	Type
low complexity region	11	26	N/A	INTRINSIC
low complexity region	34	50	N/A	INTRINSIC
low complexity region	80	107	N/A	INTRINSIC
Pfam:DUF4939	130	220	6.1e-17	PFAM
Pfam:Retrotrans_gag	174	267	2.9e-20	PFAM
low complexity region	334	342	N/A	INTRINSIC
ZnF_C2HC	345	361	3.34e-2	SMART
low complexity region	368	379	N/A	INTRINSIC
low complexity region	541	610	N/A	INTRINSIC
low complexity region	621	660	N/A	INTRINSIC
low complexity region	663	785	N/A	INTRINSIC
Blast:SERPIN	798	910	1e-5	BLAST
low complexity region	923	936	N/A	INTRINSIC
low complexity region	972	998	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000176204

SMART Domains

Protein: ENSMUSP00000134963
Gene: ENSMUSG00000092035

Domain	Start	End	E-Value	Type
low complexity region	11	26	N/A	INTRINSIC
low complexity region	34	50	N/A	INTRINSIC
low complexity region	80	107	N/A	INTRINSIC
Pfam:Retrotrans_gag	174	267	1.3e-20	PFAM
low complexity region	334	342	N/A	INTRINSIC
ZnF_C2HC	345	361	3.34e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176551

SMART Domains

Protein: ENSMUSP00000135076
Gene: ENSMUSG00000092035

Domain	Start	End	E-Value	Type
low complexity region	173	242	N/A	INTRINSIC
low complexity region	253	292	N/A	INTRINSIC
low complexity region	295	417	N/A	INTRINSIC
Blast:SERPIN	430	542	6e-6	BLAST
low complexity region	555	568	N/A	INTRINSIC
low complexity region	604	630	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.3%
20x: 95.5%

Validation Efficiency

100% (71/71)

MGI Phenotype

FUNCTION: This is a paternally expressed imprinted gene that is thought to have been derived from the Ty3/Gypsy family of retrotransposons. It contains two overlapping open reading frames, RF1 and RF2, and expresses two proteins: a shorter, gag-like protein (with a CCHC-type zinc finger domain) from RF1; and a longer, gag/pol-like fusion protein (with an additional aspartic protease motif) from RF1/RF2 by -1 translational frameshifting (-1 FS). While -1 FS has been observed in RNA viruses and transposons in both prokaryotes and eukaryotes, this gene represents the first example of -1 FS in a eukaryotic cellular gene. This gene is highly conserved across mammalian species and retains the heptanucleotide (GGGAAAC) and pseudoknot elements required for -1 FS. It is expressed in adult and embryonic tissues (most notably in placenta) and reported to have a role in cell proliferation, differentiation, apoptosis and cancer development. Knockout mice lacking this gene showed early embryonic lethality with placental defects, indicating the importance of this gene in embryonic development. [provided by RefSeq, Oct 2014]
PHENOTYPE: Heterozygous mice with a paternally inherited null allele display embryonic lethality during organogenesis with abnormal placental development. Heterozygous mice with a maternally inherited null allele are viable and fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930504O13Rik	T	A	11: 58,446,366 (GRCm38)	I94L	possibly damaging	Het
4931406P16Rik	A	T	7: 34,242,377 (GRCm38)	Y627*	probably null	Het
Actr3	A	T	1: 125,395,137 (GRCm38)	D364E	probably benign	Het
Adra2c	C	T	5: 35,280,079 (GRCm38)	T65I	probably damaging	Het
Agap2	T	A	10: 127,089,360 (GRCm38)		probably null	Het
Ager	T	C	17: 34,598,754 (GRCm38)	V126A	possibly damaging	Het
Arhgap39	T	C	15: 76,737,536 (GRCm38)	I288M	probably benign	Het
Arhgap45	A	T	10: 80,026,234 (GRCm38)	S541C	probably benign	Het
Asb4	A	G	6: 5,431,043 (GRCm38)	Y426C	probably damaging	Het
Azi2	C	T	9: 118,049,338 (GRCm38)	T82I	probably damaging	Het
Baz2b	T	A	2: 59,948,223 (GRCm38)	R764S	probably damaging	Het
Ccdc146	A	C	5: 21,301,340 (GRCm38)	I701S	probably damaging	Het
Cd55b	T	A	1: 130,418,166 (GRCm38)	I172F	probably damaging	Het
Cdk11b	A	G	4: 155,634,190 (GRCm38)	E199G	probably benign	Het
Cntnap4	A	T	8: 112,752,289 (GRCm38)	T216S	possibly damaging	Het
D5Ertd579e	A	T	5: 36,604,514 (GRCm38)	N1336K	possibly damaging	Het
Dlg5	T	C	14: 24,164,568 (GRCm38)	N649S	probably damaging	Het
Dmxl1	A	G	18: 49,846,586 (GRCm38)	E96G	probably benign	Het
Dscaml1	C	T	9: 45,668,160 (GRCm38)	T335I	possibly damaging	Het
Epb41l2	G	T	10: 25,502,124 (GRCm38)	G695C	probably damaging	Het
Erbb4	C	T	1: 68,560,576 (GRCm38)	R114H	probably damaging	Het
F2rl1	G	T	13: 95,513,938 (GRCm38)	Y145*	probably null	Het
Fam58b	T	C	11: 78,751,230 (GRCm38)	K145E	probably damaging	Het
Fsip2	A	T	2: 82,980,441 (GRCm38)	Y2368F	possibly damaging	Het
Galnt7	C	T	8: 57,536,578 (GRCm38)		probably null	Het
Gm6811	T	G	17: 21,094,690 (GRCm38)		noncoding transcript	Het
Gm6811	T	A	17: 21,093,983 (GRCm38)		noncoding transcript	Het
H2-M1	G	A	17: 36,671,710 (GRCm38)	T86M	possibly damaging	Het
Hk2	T	C	6: 82,743,366 (GRCm38)	D170G	probably benign	Het
Hmcn1	C	T	1: 150,738,681 (GRCm38)	A1325T	possibly damaging	Het
Insrr	T	A	3: 87,800,519 (GRCm38)	Y89*	probably null	Het
Itga1	T	C	13: 114,980,852 (GRCm38)	E871G	probably benign	Het
Kat6a	T	C	8: 22,939,405 (GRCm38)	L1592P	possibly damaging	Het
Kndc1	C	A	7: 139,921,063 (GRCm38)	A756E	probably benign	Het
Krt12	A	T	11: 99,421,902 (GRCm38)	C105*	probably null	Het
Lama1	G	A	17: 67,784,088 (GRCm38)		probably null	Het
Lama3	A	G	18: 12,506,949 (GRCm38)	N67S	probably benign	Het
Lrrk1	A	G	7: 66,306,839 (GRCm38)		probably null	Het
Map2	T	C	1: 66,399,419 (GRCm38)	V34A	probably damaging	Het
Mroh6	A	G	15: 75,885,700 (GRCm38)	L487P	probably damaging	Het
Myo18b	A	T	5: 112,811,642 (GRCm38)	S1430T	probably benign	Het
Notch3	G	A	17: 32,154,749 (GRCm38)	T495I	probably benign	Het
Olfr391-ps	A	T	11: 73,799,403 (GRCm38)	M118K	probably damaging	Het
Palld	C	T	8: 61,513,423 (GRCm38)	A980T	probably damaging	Het
Paxip1	A	T	5: 27,761,668 (GRCm38)	I620N	probably damaging	Het
Pcdha6	A	G	18: 36,969,767 (GRCm38)		probably null	Het
Pcdhb11	G	A	18: 37,421,760 (GRCm38)	V48M	probably benign	Het
Pcdhga6	A	G	18: 37,707,644 (GRCm38)	E139G	probably benign	Het
Pck1	T	C	2: 173,157,319 (GRCm38)	V426A	probably damaging	Het
Pck2	T	A	14: 55,542,624 (GRCm38)	I110N	probably damaging	Het
Phactr3	G	A	2: 178,279,019 (GRCm38)	E222K	probably damaging	Het
Ppip5k1	A	T	2: 121,323,203 (GRCm38)		probably benign	Het
Prodh2	A	G	7: 30,506,651 (GRCm38)	H278R	probably benign	Het
Rspry1	T	A	8: 94,623,258 (GRCm38)	H91Q	probably damaging	Het
Slc13a2	CGTTATCTGT	CGT	11: 78,403,480 (GRCm38)		probably benign	Het
Smn1	A	G	13: 100,127,995 (GRCm38)	N78S	possibly damaging	Het
Spta1	T	A	1: 174,218,512 (GRCm38)	I1614N	probably damaging	Het
Syt17	T	C	7: 118,434,290 (GRCm38)	D165G	probably damaging	Het
Tbck	A	G	3: 132,743,005 (GRCm38)	Y593C	probably damaging	Het
Tcaf2	G	C	6: 42,629,753 (GRCm38)	F422L	probably benign	Het
Tex15	T	A	8: 33,577,189 (GRCm38)	F2216I	possibly damaging	Het
Trpc4	A	G	3: 54,318,020 (GRCm38)	E846G	probably benign	Het
Ttc41	T	C	10: 86,744,449 (GRCm38)	I753T	probably benign	Het
Vdac1	C	T	11: 52,376,482 (GRCm38)	T70M	possibly damaging	Het
Vmn1r124	A	C	7: 21,260,179 (GRCm38)	F147V	probably benign	Het
Vmn1r220	T	C	13: 23,184,295 (GRCm38)	D77G	probably damaging	Het
Vmn2r28	T	C	7: 5,490,731 (GRCm38)	H72R	probably benign	Het
Vmn2r78	A	T	7: 86,921,110 (GRCm38)	I279L	probably benign	Het
Vmn2r95	G	T	17: 18,451,470 (GRCm38)	A490S	possibly damaging	Het
Wdfy4	C	T	14: 33,109,525 (GRCm38)	A915T	possibly damaging	Het
Zmiz2	G	T	11: 6,395,604 (GRCm38)		probably null	Het
Zscan2	A	G	7: 80,875,809 (GRCm38)	N426S	probably benign	Het

Other mutations in Peg10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02029:Peg10	APN	6	4,754,473 (GRCm38)	utr 5 prime	probably benign
IGL03063:Peg10	APN	6	4,756,647 (GRCm38)	utr 3 prime	probably benign
piaggio	UTSW	6	4,756,427 (GRCm38)	utr 3 prime	probably benign
PIT4480001:Peg10	UTSW	6	4,756,560 (GRCm38)	missense	unknown
R0090:Peg10	UTSW	6	4,756,063 (GRCm38)	utr 3 prime	probably benign
R0148:Peg10	UTSW	6	4,755,711 (GRCm38)	missense	possibly damaging	0.88
R0650:Peg10	UTSW	6	4,756,475 (GRCm38)	small insertion	probably benign
R0698:Peg10	UTSW	6	4,756,835 (GRCm38)	utr 3 prime	probably benign
R1600:Peg10	UTSW	6	4,757,080 (GRCm38)	utr 3 prime	probably benign
R1842:Peg10	UTSW	6	4,756,381 (GRCm38)	utr 3 prime	probably benign
R1930:Peg10	UTSW	6	4,755,778 (GRCm38)	missense	probably damaging	0.99
R1931:Peg10	UTSW	6	4,755,778 (GRCm38)	missense	probably damaging	0.99
R2162:Peg10	UTSW	6	4,755,914 (GRCm38)	utr 3 prime	probably benign
R2215:Peg10	UTSW	6	4,756,918 (GRCm38)	utr 3 prime	probably benign
R2339:Peg10	UTSW	6	4,756,102 (GRCm38)	utr 3 prime	probably benign
R2847:Peg10	UTSW	6	4,756,912 (GRCm38)	utr 3 prime	probably benign
R2848:Peg10	UTSW	6	4,756,912 (GRCm38)	utr 3 prime	probably benign
R3000:Peg10	UTSW	6	4,754,276 (GRCm38)	utr 5 prime	probably benign
R3056:Peg10	UTSW	6	4,755,029 (GRCm38)	missense	possibly damaging	0.66
R4051:Peg10	UTSW	6	4,754,534 (GRCm38)	missense	probably benign	0.00
R4059:Peg10	UTSW	6	4,756,427 (GRCm38)	utr 3 prime	probably benign
R4296:Peg10	UTSW	6	4,756,472 (GRCm38)	small insertion	probably benign
R4626:Peg10	UTSW	6	4,756,460 (GRCm38)	small insertion	probably benign
R4634:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R4679:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R4834:Peg10	UTSW	6	4,754,294 (GRCm38)	utr 5 prime	probably benign
R4982:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R4983:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R4996:Peg10	UTSW	6	4,756,454 (GRCm38)	small insertion	probably benign
R4997:Peg10	UTSW	6	4,756,457 (GRCm38)	small insertion	probably benign
R5015:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R5085:Peg10	UTSW	6	4,755,864 (GRCm38)	utr 3 prime	probably benign
R5091:Peg10	UTSW	6	4,754,511 (GRCm38)	missense	probably benign	0.01
R5231:Peg10	UTSW	6	4,756,939 (GRCm38)	utr 3 prime	probably benign
R5278:Peg10	UTSW	6	4,756,442 (GRCm38)	small deletion	probably benign
R5364:Peg10	UTSW	6	4,756,128 (GRCm38)	utr 3 prime	probably benign
R5397:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R5485:Peg10	UTSW	6	4,755,565 (GRCm38)	missense	probably benign	0.09
R5573:Peg10	UTSW	6	4,755,913 (GRCm38)	utr 3 prime	probably benign
R5710:Peg10	UTSW	6	4,756,351 (GRCm38)	small insertion	probably benign
R5710:Peg10	UTSW	6	4,756,350 (GRCm38)	small insertion	probably benign
R5736:Peg10	UTSW	6	4,754,423 (GRCm38)	missense	probably benign	0.00
R5865:Peg10	UTSW	6	4,754,375 (GRCm38)	missense	probably damaging	0.98
R6056:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6116:Peg10	UTSW	6	4,756,351 (GRCm38)	small insertion	probably benign
R6129:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6147:Peg10	UTSW	6	4,754,499 (GRCm38)	start gained	probably benign
R6171:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6194:Peg10	UTSW	6	4,756,351 (GRCm38)	small insertion	probably benign
R6197:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6207:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6215:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6281:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6287:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R6302:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6393:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6394:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R6405:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R6421:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6486:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6538:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6668:Peg10	UTSW	6	4,754,502 (GRCm38)	missense	probably benign	0.01
R6679:Peg10	UTSW	6	4,754,276 (GRCm38)	utr 5 prime	probably benign
R6685:Peg10	UTSW	6	4,754,738 (GRCm38)	missense	probably damaging	1.00
R6702:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6706:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6747:Peg10	UTSW	6	4,757,137 (GRCm38)	utr 3 prime	probably benign
R6775:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6811:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R6823:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R6826:Peg10	UTSW	6	4,756,353 (GRCm38)	small insertion	probably benign
R6847:Peg10	UTSW	6	4,754,279 (GRCm38)	utr 5 prime	probably benign
R6861:Peg10	UTSW	6	4,756,351 (GRCm38)	small insertion	probably benign
R6861:Peg10	UTSW	6	4,756,350 (GRCm38)	small insertion	probably benign
R6876:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R6891:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R6911:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R6973:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R6990:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R6998:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7070:Peg10	UTSW	6	4,756,454 (GRCm38)	small insertion	probably benign
R7120:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7132:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7140:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7189:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R7208:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7256:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7260:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7261:Peg10	UTSW	6	4,756,591 (GRCm38)	missense	unknown
R7401:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7409:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7439:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R7475:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7483:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R7502:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7515:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7520:Peg10	UTSW	6	4,756,796 (GRCm38)	missense	unknown
R7544:Peg10	UTSW	6	4,756,427 (GRCm38)	frame shift	probably null
R7571:Peg10	UTSW	6	4,756,082 (GRCm38)	missense	unknown
R7581:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7635:Peg10	UTSW	6	4,754,938 (GRCm38)	missense	probably damaging	0.99
R7677:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7697:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R7710:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7803:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R7816:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R7820:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R7827:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7861:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R7881:Peg10	UTSW	6	4,756,454 (GRCm38)	small insertion	probably benign
R7904:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R7915:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R7916:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R7963:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8016:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8037:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8062:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8081:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8113:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8115:Peg10	UTSW	6	4,756,707 (GRCm38)	missense	unknown
R8140:Peg10	UTSW	6	4,756,113 (GRCm38)	missense	unknown
R8178:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8233:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R8239:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8281:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R8310:Peg10	UTSW	6	4,756,454 (GRCm38)	small insertion	probably benign
R8312:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8330:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8338:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8354:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8387:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8390:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8408:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R8415:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8439:Peg10	UTSW	6	4,755,462 (GRCm38)	missense	possibly damaging	0.58
R8444:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8463:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R8477:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R8507:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R8552:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8678:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R8699:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8700:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8705:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8765:Peg10	UTSW	6	4,754,492 (GRCm38)	missense	unknown
R8824:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8859:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8870:Peg10	UTSW	6	4,754,825 (GRCm38)	missense	probably damaging	0.99
R8909:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R8918:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8924:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R8925:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8930:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R8950:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8960:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R8975:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R8988:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9046:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9068:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9074:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9088:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R9094:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R9114:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9116:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9135:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R9137:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9139:Peg10	UTSW	6	4,757,128 (GRCm38)	missense	unknown
R9139:Peg10	UTSW	6	4,756,449 (GRCm38)	small insertion	probably benign
R9171:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9173:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9213:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9216:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9229:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9233:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9283:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9328:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9367:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9369:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9405:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9410:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9412:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R9421:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9437:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9440:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9460:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9492:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9495:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9500:Peg10	UTSW	6	4,756,871 (GRCm38)	missense	unknown
R9511:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9515:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9576:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9610:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9611:Peg10	UTSW	6	4,756,453 (GRCm38)	small insertion	probably benign
R9611:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9614:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign
R9619:Peg10	UTSW	6	4,755,316 (GRCm38)	missense	probably benign	0.02
R9646:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9655:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9673:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
R9675:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9696:Peg10	UTSW	6	4,756,431 (GRCm38)	small deletion	probably benign
R9749:Peg10	UTSW	6	4,756,398 (GRCm38)	small deletion	probably benign
R9756:Peg10	UTSW	6	4,756,452 (GRCm38)	small insertion	probably benign
X0065:Peg10	UTSW	6	4,756,515 (GRCm38)	utr 3 prime	probably benign
Z1176:Peg10	UTSW	6	4,756,451 (GRCm38)	small insertion	probably benign

Predicted Primers

PCR Primer
(F):5'- GTTTACAGTGCCACAACCG -3'
(R):5'- ACAGGGTGGTAAATTCTGAATCC -3'

Sequencing Primer
(F):5'- TCAGCATGAGCATCTGCATG -3'
(R):5'- CTGAATCCAGCCATGTGGTAG -3'

Posted On

2018-03-15