Mutagenetix > Incidental Mutation

Incidental Mutation 'R8239:Peg10'

637497

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

067646-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8239 (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: 99.8%
10x: 99.5%
20x: 98.9%

Validation Efficiency

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: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam39	T	C	8: 41,278,106 (GRCm39)	S166P	probably damaging	Het
Appl1	T	A	14: 26,686,914 (GRCm39)	T19S	probably damaging	Het
Arid4b	T	A	13: 14,344,594 (GRCm39)	D557E	probably benign	Het
Aven	C	T	2: 112,390,120 (GRCm39)	R8W	probably benign	Het
C2cd2l	T	C	9: 44,227,502 (GRCm39)	E307G	possibly damaging	Het
Cdh20	A	C	1: 110,027,832 (GRCm39)	T526P	probably benign	Het
Dchs1	C	T	7: 105,414,718 (GRCm39)	V775M	probably benign	Het
Dennd1b	A	G	1: 138,969,673 (GRCm39)	N63S	probably benign	Het
Dtnb	A	T	12: 3,694,056 (GRCm39)	Y248F	unknown	Het
Ehbp1l1	T	A	19: 5,770,089 (GRCm39)	T405S	possibly damaging	Het
Fam149a	A	G	8: 45,803,490 (GRCm39)	Y415H	possibly damaging	Het
Fam186a	A	G	15: 99,839,191 (GRCm39)	L2351P	unknown	Het
Fsip2	T	G	2: 82,819,687 (GRCm39)	I5140S	possibly damaging	Het
Gm8674	T	C	13: 50,054,262 (GRCm39)	T749A	noncoding transcript	Het
Kalrn	A	G	16: 33,870,153 (GRCm39)	V1894A	noncoding transcript	Het
Kpna3	A	T	14: 61,624,919 (GRCm39)	N141K	probably damaging	Het
Lrba	G	A	3: 86,449,882 (GRCm39)	G2067D	probably damaging	Het
Lrp2	G	T	2: 69,311,611 (GRCm39)	Y2622*	probably null	Het
Lrtm2	A	C	6: 119,297,778 (GRCm39)	F88V	probably damaging	Het
Mboat1	T	C	13: 30,429,333 (GRCm39)	S454P	probably damaging	Het
Nkpd1	C	T	7: 19,253,753 (GRCm39)	P40S	probably benign	Het
Or2b7	T	C	13: 21,739,788 (GRCm39)	I135V	probably benign	Het
Or4a76	T	A	2: 89,460,907 (GRCm39)	I112F	probably damaging	Het
Or8b54	G	A	9: 38,686,577 (GRCm39)	V9M	noncoding transcript	Het
Or8k27	C	A	2: 86,275,473 (GRCm39)	M284I	noncoding transcript	Het
Patj	A	G	4: 98,570,308 (GRCm39)	E1711G	possibly damaging	Het
Pcdha4	A	T	18: 37,086,128 (GRCm39)	I104F	probably damaging	Het
Plekhg4	C	T	8: 106,107,546 (GRCm39)	R990*	probably null	Het
Pphln1	T	C	15: 93,386,930 (GRCm39)	S343P	probably benign	Het
Pram1	A	T	17: 33,860,241 (GRCm39)	K269N	probably damaging	Het
Psmd13	T	A	7: 140,466,450 (GRCm39)	I79K	probably damaging	Het
Ptprf	T	C	4: 118,069,309 (GRCm39)	D1586G	possibly damaging	Het
Ptprh	T	A	7: 4,584,090 (GRCm39)	Q167H	probably damaging	Het
Rbm46	C	T	3: 82,772,775 (GRCm39)	R119Q	probably benign	Het
Rreb1	T	C	13: 38,077,848 (GRCm39)	M20T	probably damaging	Het
Scrn2	T	G	11: 96,923,046 (GRCm39)	L163R	probably damaging	Het
Slc36a3	C	T	11: 55,022,433 (GRCm39)	V254I	probably benign	Het
Slc6a6	T	C	6: 91,701,951 (GRCm39)	F120L	probably benign	Het
Slc8a2	A	T	7: 15,879,230 (GRCm39)	H572L	probably benign	Het
Spats2	T	A	15: 99,106,776 (GRCm39)	D357E	probably damaging	Het
Speg	A	T	1: 75,395,677 (GRCm39)	N1816I	probably damaging	Het
Sult2b1	A	G	7: 45,433,361 (GRCm39)	V2A	unknown	Het
Susd3	T	C	13: 49,384,731 (GRCm39)	T231A	probably benign	Het
Tamalin	C	T	15: 101,128,902 (GRCm39)	L217F	probably damaging	Het
Tcp1	A	G	17: 13,139,738 (GRCm39)	D261G	probably benign	Het
Trpm2	C	G	10: 77,771,836 (GRCm39)	S601T	probably benign	Het
Ugt2b38	A	T	5: 87,571,659 (GRCm39)	F124L	probably benign	Het
Unc80	G	T	1: 66,693,178 (GRCm39)	E2522D	probably benign	Het
Usp34	A	G	11: 23,396,750 (GRCm39)	T2365A		Het
Vmn2r92	G	T	17: 18,405,278 (GRCm39)	M807I	probably benign	Het
Vps13b	C	A	15: 35,597,550 (GRCm39)	P1030Q	probably damaging	Het
Wrn	T	G	8: 33,819,213 (GRCm39)	K246N	probably damaging	Het
Zer1	T	A	2: 29,991,147 (GRCm39)		probably null	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
R6702:Peg10	UTSW	6	4,756,452 (GRCm39)	small insertion	probably benign
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
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'- GTTTACAGTGCCACAACCG -3'
(R):5'- ACCTTACAGGGTGGTAAATTCTG -3'

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

Posted On

2020-07-13