Mutagenetix > Incidental Mutation

Incidental Mutation 'R6702:Peg10'

528804

Institutional Source

Beutler Lab

Gene Symbol

Peg10

Ensembl Gene

ENSMUSG00000092035

Gene Name

paternally expressed 10

Synonyms

MEF3L, MyEF-3 like, Rtl2, Mar2, MyEF-3, HB-1, Edr, Mart2

MMRRC Submission

044820-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6702 (G1)

Quality Score

217.468

Status

Not validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm39)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

GC to GCTCC at 4756452 bp (GRCm39)

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

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.5%

Validation Efficiency

97% (59/61)

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: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020N01Rik	T	A	10: 21,497,558 (GRCm39)	Y66*	probably null	Het
Ak3	A	G	19: 29,003,627 (GRCm39)	V183A	probably damaging	Het
Ano10	G	T	9: 122,088,630 (GRCm39)	Q397K	possibly damaging	Het
Atg7	C	A	6: 114,648,058 (GRCm39)		probably null	Het
Brpf3	A	C	17: 29,029,633 (GRCm39)	N531T	probably benign	Het
Casp2	T	C	6: 42,244,985 (GRCm39)	V128A	probably benign	Het
Cdcp2	T	C	4: 106,964,283 (GRCm39)	C378R	probably benign	Het
Cfap54	T	A	10: 92,704,596 (GRCm39)	D2828V	unknown	Het
Col6a3	T	C	1: 90,707,161 (GRCm39)	D1984G	unknown	Het
Csnk2a1	A	G	2: 152,100,608 (GRCm39)	T93A	probably benign	Het
Ddx54	T	A	5: 120,764,568 (GRCm39)	D758E	possibly damaging	Het
Dlx2	A	G	2: 71,376,571 (GRCm39)	S56P	probably damaging	Het
Dna2	T	A	10: 62,809,073 (GRCm39)	I1055N	possibly damaging	Het
Dnah10	A	G	5: 124,882,869 (GRCm39)	Y2909C	probably damaging	Het
Dnm3	A	G	1: 162,146,256 (GRCm39)	F296L	probably benign	Het
Fat1	A	G	8: 45,406,083 (GRCm39)	T945A	probably benign	Het
Herpud1	T	C	8: 95,119,154 (GRCm39)		probably null	Het
Iqub	T	A	6: 24,449,744 (GRCm39)	N707I	probably damaging	Het
Kif26b	C	G	1: 178,744,852 (GRCm39)	S1649R	possibly damaging	Het
Lamp5	C	G	2: 135,901,483 (GRCm39)	N102K	possibly damaging	Het
Ltbr	A	G	6: 125,285,031 (GRCm39)	S290P	probably benign	Het
Map4k1	T	G	7: 28,701,821 (GRCm39)	S803A	possibly damaging	Het
Mef2c	T	A	13: 83,773,525 (GRCm39)	C134S	possibly damaging	Het
Myo15a	A	G	11: 60,383,818 (GRCm39)	I1622V	probably benign	Het
Nbea	A	G	3: 55,912,923 (GRCm39)	Y955H	probably benign	Het
Ndor1	A	G	2: 25,139,902 (GRCm39)	F142S	possibly damaging	Het
Nynrin	A	G	14: 56,101,935 (GRCm39)	T535A	possibly damaging	Het
Or4k15	A	G	14: 50,364,688 (GRCm39)	Y218C	probably damaging	Het
Or4k42	T	A	2: 111,320,454 (GRCm39)		probably null	Het
Or5ac23	C	T	16: 59,148,961 (GRCm39)	V304I	probably benign	Het
Or5d46	G	A	2: 88,170,586 (GRCm39)	V226I	probably benign	Het
Or8b51	A	T	9: 38,569,073 (GRCm39)	I205N	possibly damaging	Het
Pcdhb13	T	G	18: 37,577,828 (GRCm39)	H735Q	probably benign	Het
Pcdhb7	A	T	18: 37,474,959 (GRCm39)	M32L	probably benign	Het
Per2	C	T	1: 91,355,671 (GRCm39)	E696K	probably damaging	Het
Pld4	T	C	12: 112,731,485 (GRCm39)	S213P	probably damaging	Het
Prkg1	T	A	19: 30,970,484 (GRCm39)	H209L	probably benign	Het
Psg16	T	C	7: 16,824,321 (GRCm39)	L35P	probably damaging	Het
Pxn	C	T	5: 115,689,955 (GRCm39)	L160F	probably benign	Het
Rab3a	A	G	8: 71,209,095 (GRCm39)	D77G	probably damaging	Het
Resf1	T	A	6: 149,229,376 (GRCm39)	N807K	probably damaging	Het
Rgma	A	T	7: 73,067,068 (GRCm39)	T108S	probably damaging	Het
Rxrg	A	G	1: 167,441,374 (GRCm39)	S51G	probably benign	Het
S1pr3	A	T	13: 51,573,475 (GRCm39)	I219F	probably damaging	Het
Sec23b	A	T	2: 144,401,109 (GRCm39)		probably null	Het
Sfrp5	G	T	19: 42,190,266 (GRCm39)	T62K	probably benign	Het
Slco1a6	T	A	6: 142,048,826 (GRCm39)	Y318F	probably damaging	Het
Slit1	A	C	19: 41,603,309 (GRCm39)	S931A	possibly damaging	Het
Sorl1	A	T	9: 41,982,497 (GRCm39)	V361E	probably damaging	Het
St6galnac2	A	G	11: 116,575,213 (GRCm39)	S209P	probably benign	Het
Supt6	C	A	11: 78,122,626 (GRCm39)	R199L	possibly damaging	Het
Tas2r107	A	C	6: 131,636,347 (GRCm39)	M234R	probably benign	Het
Tmem72	C	G	6: 116,675,310 (GRCm39)	V61L	probably benign	Het
Trpm5	C	A	7: 142,623,055 (GRCm39)		probably benign	Het
Ttn	T	G	2: 76,550,456 (GRCm39)	T23282P	probably damaging	Het
Ubap2	GCCCGCTTGCCCCGCT	GCCCGCTTGCCCCGCTTGCCCCGCT	4: 41,227,210 (GRCm39)		probably benign	Het
Ubr3	A	T	2: 69,786,393 (GRCm39)	R836W	probably benign	Het
Umodl1	A	G	17: 31,205,273 (GRCm39)		probably null	Het
Ythdf1	A	G	2: 180,560,926 (GRCm39)		probably null	Het
Zfp780b	T	C	7: 27,671,066 (GRCm39)	T81A	possibly damaging	Het
Zfp811	T	C	17: 33,016,816 (GRCm39)	E407G	probably damaging	Het

Other mutations in Peg10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02029:Peg10	APN	6	4,754,473 (GRCm39)	utr 5 prime	probably benign
IGL03063:Peg10	APN	6	4,756,647 (GRCm39)	utr 3 prime	probably benign
piaggio	UTSW	6	4,756,427 (GRCm39)	utr 3 prime	probably benign
PIT4480001:Peg10	UTSW	6	4,756,560 (GRCm39)	missense	unknown
R0090:Peg10	UTSW	6	4,756,063 (GRCm39)	utr 3 prime	probably benign
R0148:Peg10	UTSW	6	4,755,711 (GRCm39)	missense	possibly damaging	0.88
R0650:Peg10	UTSW	6	4,756,475 (GRCm39)	small insertion	probably benign
R0698:Peg10	UTSW	6	4,756,835 (GRCm39)	utr 3 prime	probably benign
R1600:Peg10	UTSW	6	4,757,080 (GRCm39)	utr 3 prime	probably benign
R1842:Peg10	UTSW	6	4,756,381 (GRCm39)	utr 3 prime	probably benign
R1930:Peg10	UTSW	6	4,755,778 (GRCm39)	missense	probably damaging	0.99
R1931:Peg10	UTSW	6	4,755,778 (GRCm39)	missense	probably damaging	0.99
R2162:Peg10	UTSW	6	4,755,914 (GRCm39)	utr 3 prime	probably benign
R2215:Peg10	UTSW	6	4,756,918 (GRCm39)	utr 3 prime	probably benign
R2339:Peg10	UTSW	6	4,756,102 (GRCm39)	utr 3 prime	probably benign
R2847:Peg10	UTSW	6	4,756,912 (GRCm39)	utr 3 prime	probably benign
R2848:Peg10	UTSW	6	4,756,912 (GRCm39)	utr 3 prime	probably benign
R3000:Peg10	UTSW	6	4,754,276 (GRCm39)	utr 5 prime	probably benign
R3056:Peg10	UTSW	6	4,755,029 (GRCm39)	missense	possibly damaging	0.66
R4051:Peg10	UTSW	6	4,754,534 (GRCm39)	missense	probably benign	0.00
R4059:Peg10	UTSW	6	4,756,427 (GRCm39)	utr 3 prime	probably benign
R4296:Peg10	UTSW	6	4,756,472 (GRCm39)	small insertion	probably benign
R4626:Peg10	UTSW	6	4,756,460 (GRCm39)	small insertion	probably benign
R4634:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R4679:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R4834:Peg10	UTSW	6	4,754,294 (GRCm39)	utr 5 prime	probably benign
R4982:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R4983:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R4996:Peg10	UTSW	6	4,756,454 (GRCm39)	small insertion	probably benign
R4997:Peg10	UTSW	6	4,756,457 (GRCm39)	small insertion	probably benign
R5015:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R5085:Peg10	UTSW	6	4,755,864 (GRCm39)	utr 3 prime	probably benign
R5091:Peg10	UTSW	6	4,754,511 (GRCm39)	missense	probably benign	0.01
R5231:Peg10	UTSW	6	4,756,939 (GRCm39)	utr 3 prime	probably benign
R5278:Peg10	UTSW	6	4,756,442 (GRCm39)	small deletion	probably benign
R5364:Peg10	UTSW	6	4,756,128 (GRCm39)	utr 3 prime	probably benign
R5397:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R5485:Peg10	UTSW	6	4,755,565 (GRCm39)	missense	probably benign	0.09
R5573:Peg10	UTSW	6	4,755,913 (GRCm39)	utr 3 prime	probably benign
R5710:Peg10	UTSW	6	4,756,351 (GRCm39)	small insertion	probably benign
R5710:Peg10	UTSW	6	4,756,350 (GRCm39)	small insertion	probably benign
R5736:Peg10	UTSW	6	4,754,423 (GRCm39)	missense	probably benign	0.00
R5865:Peg10	UTSW	6	4,754,375 (GRCm39)	missense	probably damaging	0.98
R6056:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6116:Peg10	UTSW	6	4,756,351 (GRCm39)	small insertion	probably benign
R6129:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6147:Peg10	UTSW	6	4,754,499 (GRCm39)	start gained	probably benign
R6171:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6194:Peg10	UTSW	6	4,756,351 (GRCm39)	small insertion	probably benign
R6197:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6207:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6215:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6276:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6281:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6287:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R6302:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6393:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6394:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R6405:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R6421:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6486:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6538:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6668:Peg10	UTSW	6	4,754,502 (GRCm39)	missense	probably benign	0.01
R6679:Peg10	UTSW	6	4,754,276 (GRCm39)	utr 5 prime	probably benign
R6685:Peg10	UTSW	6	4,754,738 (GRCm39)	missense	probably damaging	1.00
R6706:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6747:Peg10	UTSW	6	4,757,137 (GRCm39)	utr 3 prime	probably benign
R6775:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6811:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R6823:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R6826:Peg10	UTSW	6	4,756,353 (GRCm39)	small insertion	probably benign
R6847:Peg10	UTSW	6	4,754,279 (GRCm39)	utr 5 prime	probably benign
R6861:Peg10	UTSW	6	4,756,351 (GRCm39)	small insertion	probably benign
R6861:Peg10	UTSW	6	4,756,350 (GRCm39)	small insertion	probably benign
R6876:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R6891:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R6911:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R6973:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R6990:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R6998:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7070:Peg10	UTSW	6	4,756,454 (GRCm39)	small insertion	probably benign
R7120:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7132:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7140:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7189:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R7208:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7256:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7260:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7261:Peg10	UTSW	6	4,756,591 (GRCm39)	missense	unknown
R7401:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7409:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7439:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R7475:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7483:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R7502:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7515:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7520:Peg10	UTSW	6	4,756,796 (GRCm39)	missense	unknown
R7544:Peg10	UTSW	6	4,756,427 (GRCm39)	frame shift	probably null
R7571:Peg10	UTSW	6	4,756,082 (GRCm39)	missense	unknown
R7581:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7635:Peg10	UTSW	6	4,754,938 (GRCm39)	missense	probably damaging	0.99
R7677:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7697:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R7710:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7803:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R7816:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R7820:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R7827:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7861:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R7881:Peg10	UTSW	6	4,756,454 (GRCm39)	small insertion	probably benign
R7904:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R7915:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R7916:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R7963:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8016:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8037:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8062:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8081:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8113:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8115:Peg10	UTSW	6	4,756,707 (GRCm39)	missense	unknown
R8140:Peg10	UTSW	6	4,756,113 (GRCm39)	missense	unknown
R8178:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8233:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R8239:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8281:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R8310:Peg10	UTSW	6	4,756,454 (GRCm39)	small insertion	probably benign
R8312:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8330:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8338:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8354:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8387:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8390:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8408:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R8415:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8439:Peg10	UTSW	6	4,755,462 (GRCm39)	missense	possibly damaging	0.58
R8444:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8463:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R8477:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R8507:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R8552:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8678:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R8699:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8700:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8705:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8765:Peg10	UTSW	6	4,754,492 (GRCm39)	missense	unknown
R8824:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8859:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8870:Peg10	UTSW	6	4,754,825 (GRCm39)	missense	probably damaging	0.99
R8909:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R8918:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8924:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R8925:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8930:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R8950:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8960:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R8975:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R8988:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9046:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9068:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9074:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9088:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R9094:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R9114:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9116:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9135:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R9137:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9139:Peg10	UTSW	6	4,757,128 (GRCm39)	missense	unknown
R9139:Peg10	UTSW	6	4,756,449 (GRCm39)	small insertion	probably benign
R9171:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9173:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9213:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9216:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9229:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9233:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9283:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9328:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9367:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9369:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9405:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9410:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9412:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R9421:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9437:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9440:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9460:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9492:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9495:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9500:Peg10	UTSW	6	4,756,871 (GRCm39)	missense	unknown
R9511:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9515:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9576:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9610:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9611:Peg10	UTSW	6	4,756,453 (GRCm39)	small insertion	probably benign
R9611:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9614:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign
R9619:Peg10	UTSW	6	4,755,316 (GRCm39)	missense	probably benign	0.02
R9646:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9655:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9673:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
R9675:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9696:Peg10	UTSW	6	4,756,431 (GRCm39)	small deletion	probably benign
R9749:Peg10	UTSW	6	4,756,398 (GRCm39)	small deletion	probably benign
R9756:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
X0065:Peg10	UTSW	6	4,756,515 (GRCm39)	utr 3 prime	probably benign
Z1176:Peg10	UTSW	6	4,756,451 (GRCm39)	small insertion	probably benign

Predicted Primers

PCR Primer
(F):5'- CTGTTTACAGTGCCACAACCG -3'
(R):5'- ACCTTACAGGGTGGTAAATTCTG -3'

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

Posted On

2018-07-24