Mutagenetix > Incidental Mutation

Incidental Mutation 'R6747:Peg10'

530579

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

044864-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6747 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm38)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

A to G at 4757137 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000134963 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000166678
AA Change: Q972R

SMART Domains

Protein: ENSMUSP00000127306
Gene: ENSMUSG00000092035
AA Change: Q972R

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

unknown
Transcript: ENSMUST00000176551
AA Change: Q571R

SMART Domains

Protein: ENSMUSP00000135076
Gene: ENSMUSG00000092035
AA Change: Q571R

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: 98.5%
20x: 96.0%

Validation Efficiency

97% (68/70)

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: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	C	T	3: 122,126,313 (GRCm38)		probably null	Het
Acyp1	C	T	12: 85,278,905 (GRCm38)	V107I	probably null	Het
Aftph	T	C	11: 20,726,144 (GRCm38)		probably null	Het
Agtpbp1	A	T	13: 59,544,353 (GRCm38)		probably null	Het
Arhgap15	C	A	2: 44,116,677 (GRCm38)	P269T	probably damaging	Het
Arhgap30	T	C	1: 171,407,729 (GRCm38)	V557A	probably damaging	Het
Asb3	T	A	11: 31,081,493 (GRCm38)	M410K	probably benign	Het
B4galnt2	T	C	11: 95,868,634 (GRCm38)		probably null	Het
Birc3	A	G	9: 7,860,261 (GRCm38)		probably null	Het
Cav2	A	T	6: 17,286,951 (GRCm38)	N69Y	probably damaging	Het
Cc2d2b	G	A	19: 40,795,667 (GRCm38)	C826Y	probably benign	Het
Cenpf	T	A	1: 189,652,854 (GRCm38)	T2410S	probably benign	Het
Chchd1	A	G	14: 20,703,380 (GRCm38)	D24G	probably benign	Het
Cmip	G	A	8: 117,436,879 (GRCm38)	G450S	probably benign	Het
Col11a1	C	T	3: 114,212,450 (GRCm38)	Q534*	probably null	Het
Col3a1	G	T	1: 45,338,622 (GRCm38)		probably benign	Het
Cox4i1	T	C	8: 120,673,230 (GRCm38)	I31T	possibly damaging	Het
Cstf3	G	T	2: 104,646,767 (GRCm38)	V168F	probably damaging	Het
Dapk1	T	C	13: 60,725,340 (GRCm38)	I352T	probably benign	Het
Ddx52	T	C	11: 83,955,302 (GRCm38)	V456A	probably damaging	Het
Dmxl2	A	T	9: 54,416,088 (GRCm38)	H1337Q	probably damaging	Het
Dnah7a	T	C	1: 53,636,062 (GRCm38)	T369A	probably benign	Het
Dppa1	T	A	11: 46,625,595 (GRCm38)	I8F	unknown	Het
Ebf1	G	T	11: 44,883,814 (GRCm38)	V213F	probably damaging	Het
Foxb2	C	A	19: 16,872,833 (GRCm38)	E270*	probably null	Het
Gclc	A	T	9: 77,788,245 (GRCm38)	R450W	probably damaging	Het
Gm13128	T	C	4: 144,332,978 (GRCm38)	W420R	probably benign	Het
Grin2d	T	C	7: 45,862,268 (GRCm38)	E251G	probably damaging	Het
Hal	A	T	10: 93,500,677 (GRCm38)	N423Y	probably damaging	Het
Krtap4-8	T	A	11: 99,780,091 (GRCm38)	I185F	unknown	Het
Lrp3	T	A	7: 35,211,437 (GRCm38)	Q61L	probably benign	Het
Met	A	C	6: 17,571,467 (GRCm38)	Q1296H	probably damaging	Het
Mphosph9	T	A	5: 124,297,699 (GRCm38)	N557I	possibly damaging	Het
Mrpl46	C	A	7: 78,782,981 (GRCm38)	W16C	probably benign	Het
Myh13	G	A	11: 67,350,419 (GRCm38)	R874Q	probably damaging	Het
Nelfb	G	A	2: 25,203,381 (GRCm38)	T453I	probably benign	Het
Nos2	A	G	11: 78,952,954 (GRCm38)	D909G	probably damaging	Het
Nr5a2	T	C	1: 136,882,344 (GRCm38)	E431G	possibly damaging	Het
Nsmce2	A	G	15: 59,591,724 (GRCm38)	D149G	probably benign	Het
Olfr203	T	C	16: 59,303,641 (GRCm38)	F164L	probably benign	Het
Olfr690	C	T	7: 105,330,027 (GRCm38)	R55H	probably benign	Het
Pcbp4	C	A	9: 106,460,648 (GRCm38)		probably null	Het
Pms2	C	T	5: 143,925,419 (GRCm38)	P154L	probably benign	Het
Pou6f2	A	C	13: 18,129,187 (GRCm38)	L112R	probably benign	Het
Prdm6	A	T	18: 53,465,046 (GRCm38)		probably benign	Het
Prob1	G	A	18: 35,655,154 (GRCm38)	R12W	probably damaging	Het
Rif1	T	A	2: 52,078,263 (GRCm38)		probably null	Het
Rpl9-ps6	A	G	19: 32,466,143 (GRCm38)	S137P	probably benign	Het
Rsf1	GGCG	GGCGACGGCAGCG	7: 97,579,906 (GRCm38)		probably benign	Homo
Sec23ip	A	G	7: 128,752,849 (GRCm38)		silent	Het
Slc38a9	T	C	13: 112,690,180 (GRCm38)	C151R	probably benign	Het
Slc39a8	T	C	3: 135,849,180 (GRCm38)		probably null	Het
Slc6a18	C	A	13: 73,677,991 (GRCm38)		probably benign	Het
Snw1	T	C	12: 87,464,710 (GRCm38)	D57G	probably damaging	Het
Sox6	C	G	7: 115,541,731 (GRCm38)	R505P	probably damaging	Het
Speg	T	C	1: 75,410,395 (GRCm38)		probably null	Het
Spire2	C	T	8: 123,356,846 (GRCm38)	R190C	probably damaging	Het
Stard9	A	C	2: 120,698,383 (GRCm38)	H1707P	possibly damaging	Het
Tenm3	G	T	8: 48,343,243 (GRCm38)	T237K	probably damaging	Het
Themis2	T	A	4: 132,796,262 (GRCm38)	E31V	possibly damaging	Het
Trim56	T	G	5: 137,114,521 (GRCm38)	Q47P	probably damaging	Het
Trim58	T	C	11: 58,651,264 (GRCm38)	I350T	probably benign	Het
Ttll7	C	T	3: 146,944,056 (GRCm38)	P639S	probably benign	Het
Ubxn6	A	G	17: 56,070,650 (GRCm38)		probably null	Het
Vmn2r114	A	T	17: 23,309,876 (GRCm38)	F417L	probably benign	Het
Vmn2r29	T	A	7: 7,231,422 (GRCm38)	M822L	probably benign	Het
Vps9d1	T	C	8: 123,254,007 (GRCm38)	D27G	probably damaging	Het
Wdr3	C	T	3: 100,138,724 (GRCm38)	R931Q	probably damaging	Het
Whamm	G	A	7: 81,578,302 (GRCm38)		probably null	Het
Zcchc24	T	C	14: 25,757,033 (GRCm38)	H142R	probably damaging	Het
Zfp292	T	C	4: 34,806,894 (GRCm38)	K2050R	probably damaging	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
R6276:Peg10	UTSW	6	4,756,449 (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
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'- GTGGCACCATCCAAAATCAG -3'
(R):5'- CAGTCATAGATTGAGAAGCTGCAC -3'

Sequencing Primer
(F):5'- AATCAGTACCTACGCATGTCTC -3'
(R):5'- AGCTGCACAGGATCAAGTTG -3'

Posted On

2018-08-01