Mutagenetix > Incidental Mutation

Incidental Mutation 'R9495:Peg10'

717149

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

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9495 (G1)

Quality Score

122.467

Status

Not validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm38)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

T to TCCC at 4756451 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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

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: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700088E04Rik	T	A	15: 79,135,642 (GRCm38)	D158V	probably benign	Het
2200002D01Rik	CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC	CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC	7: 29,247,623 (GRCm38)		probably benign	Het
Aadacl2fm1	T	C	3: 59,932,693 (GRCm38)	I62T	possibly damaging	Het
Acp5	G	A	9: 22,127,187 (GRCm38)	Q273*	probably null	Het
Apoa5	G	C	9: 46,270,646 (GRCm38)	R340P	probably damaging	Het
Atp2b1	T	A	10: 98,999,798 (GRCm38)	N468K	probably damaging	Het
Bltp3a	A	G	17: 27,893,440 (GRCm38)	D1201G	probably damaging	Het
Bphl	A	T	13: 34,050,329 (GRCm38)	I143L	probably benign	Het
Cd33	A	T	7: 43,532,726 (GRCm38)	H98Q	probably benign	Het
Celsr1	G	T	15: 86,033,085 (GRCm38)	S229*	probably null	Het
Cemip2	T	A	19: 21,801,885 (GRCm38)	V353D	probably damaging	Het
Cfap96	C	T	8: 45,956,421 (GRCm38)	S287N	probably damaging	Het
Colec10	A	G	15: 54,462,365 (GRCm38)	D197G	probably damaging	Het
Cpt1a	T	C	19: 3,383,795 (GRCm38)	M759T	probably benign	Het
Ctc1	A	G	11: 69,022,767 (GRCm38)	Y165C	probably damaging	Het
Cyp2t4	G	A	7: 27,155,292 (GRCm38)	V66M	possibly damaging	Het
Dnah2	T	C	11: 69,454,382 (GRCm38)	D2667G	possibly damaging	Het
Dok1	T	C	6: 83,032,991 (GRCm38)	K46E	probably damaging	Het
Erv3	C	A	2: 131,856,055 (GRCm38)	W128L	possibly damaging	Het
Fam186a	A	G	15: 99,946,885 (GRCm38)	S493P	unknown	Het
Fbn1	A	T	2: 125,319,064 (GRCm38)	N2185K	probably damaging	Het
Figla	A	C	6: 86,020,707 (GRCm38)	H139P	probably benign	Het
Gemin4	A	G	11: 76,210,923 (GRCm38)	L1004P	probably damaging	Het
Gm11937	T	C	11: 99,609,820 (GRCm38)	T124A	unknown	Het
Gm17669	G	T	18: 67,562,612 (GRCm38)	V76L	probably benign	Het
H2ac21	A	G	3: 96,220,085 (GRCm38)	E57G	probably damaging	Het
Hcls1	A	T	16: 36,957,340 (GRCm38)	M274L	probably benign	Het
Il17rc	T	C	6: 113,472,780 (GRCm38)	S116P	probably damaging	Het
Krt79	G	A	15: 101,931,853 (GRCm38)	R303C	probably damaging	Het
Lamb2	C	T	9: 108,480,807 (GRCm38)	T149I	probably damaging	Het
Lrrc41	T	A	4: 116,075,609 (GRCm38)		probably null	Het
Mga	C	A	2: 119,951,195 (GRCm38)	T2234K	possibly damaging	Het
Mix23	A	G	16: 36,072,121 (GRCm38)	E12G	probably benign	Het
Muc6	T	A	7: 141,651,133 (GRCm38)	Q205L	probably damaging	Het
Nlrp9b	A	T	7: 20,026,537 (GRCm38)	K624N	possibly damaging	Het
Or1o4	G	T	17: 37,280,495 (GRCm38)		probably benign	Het
Or4d2	C	T	11: 87,893,256 (GRCm38)	V223M	probably benign	Het
Or6e1	T	C	14: 54,282,680 (GRCm38)	T72A	probably damaging	Het
Otud4	T	C	8: 79,673,458 (GRCm38)	S934P	probably damaging	Het
Pcdha12	G	T	18: 37,022,473 (GRCm38)	W748C	probably damaging	Het
Pdc	T	C	1: 150,333,168 (GRCm38)	I134T	probably damaging	Het
Pkn1	C	T	8: 83,684,170 (GRCm38)	R276Q	possibly damaging	Het
Plin3	C	A	17: 56,280,824 (GRCm38)	G297V	probably benign	Het
Podn	C	T	4: 108,018,909 (GRCm38)	V517I	probably benign	Het
Pomk	T	C	8: 25,983,316 (GRCm38)	D203G	probably damaging	Het
Ppil4	A	G	10: 7,799,591 (GRCm38)	D168G	probably damaging	Het
Ptgr2	T	C	12: 84,307,873 (GRCm38)	I276T	probably benign	Het
Ptk7	T	A	17: 46,576,818 (GRCm38)	I563F	possibly damaging	Het
Rbm12	G	T	2: 156,097,818 (GRCm38)	T178K	unknown	Het
Sctr	T	C	1: 120,031,673 (GRCm38)		probably null	Het
Sh2b1	GGGACC	GGGACCGGCTCAGCCACGTGGACC	7: 126,467,572 (GRCm38)		probably benign	Het
Spata31e4	T	A	13: 50,701,429 (GRCm38)	S368T	possibly damaging	Het
Steap1	A	T	5: 5,736,458 (GRCm38)	D326E	probably damaging	Het
Stra6	G	A	9: 58,151,892 (GRCm38)	V513I	probably benign	Het
Tbx19	A	G	1: 165,138,977 (GRCm38)	S443P	unknown	Het
Tcea3	T	A	4: 136,264,574 (GRCm38)	C190S	probably damaging	Het
Tfr2	G	A	5: 137,574,439 (GRCm38)	V171I	probably benign	Het
Tm7sf3	C	T	6: 146,623,681 (GRCm38)	D89N	possibly damaging	Het
Tmem129	A	G	5: 33,657,778 (GRCm38)	V17A	probably benign	Het
Tmem87b	T	C	2: 128,818,433 (GRCm38)	L32P	probably damaging	Het
Tor1aip1	T	A	1: 156,030,431 (GRCm38)	D205V	probably damaging	Het
Trim33	T	C	3: 103,331,758 (GRCm38)	V684A	probably benign	Het
Triobp	C	T	15: 78,993,178 (GRCm38)	R1637C	probably damaging	Het
Ulbp1	C	A	10: 7,456,371 (GRCm38)	M196I	probably benign	Het
Vash1	G	A	12: 86,691,889 (GRCm38)	G370E	probably damaging	Het
Vmn2r23	A	G	6: 123,712,713 (GRCm38)	T183A	probably benign	Het
Vta1	A	G	10: 14,655,839 (GRCm38)	I264T	probably benign	Het
Zcchc8	A	T	5: 123,700,570 (GRCm38)	M635K	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
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
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
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'- TGTTTACAGTGCCACAACCG -3'
(R):5'- ACCTTACAGGGTGGTAAATTCTG -3'

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

Posted On

2022-07-18