Mutagenetix > Incidental Mutation

Incidental Mutation 'R9094:Peg10'

691205

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

068909-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9094 (G1)

Quality Score

113.467

Status

Validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm39)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

GAT to GATCAT at 4756449 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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

96% (67/70)

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: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110021N24Rik	T	C	4: 108,637,744 (GRCm39)	V37A	unknown	Het
3425401B19Rik	G	A	14: 32,382,614 (GRCm39)	S1117L	possibly damaging	Het
Abi3bp	A	G	16: 56,456,590 (GRCm39)	I1021V	probably benign	Het
Agrn	C	A	4: 156,253,264 (GRCm39)	K1848N	probably benign	Het
Anln	A	G	9: 22,249,283 (GRCm39)	V1005A	probably benign	Het
Arb2a	A	G	13: 78,311,725 (GRCm39)	K356R	possibly damaging	Het
Arid3b	A	G	9: 57,741,327 (GRCm39)	Y40H	probably damaging	Het
Bco1	A	C	8: 117,859,917 (GRCm39)	D540A	probably benign	Het
Blnk	A	G	19: 40,982,482 (GRCm39)	I7T	probably benign	Het
Brca2	T	G	5: 150,475,770 (GRCm39)	D2493E	probably benign	Het
Bsn	T	A	9: 107,988,052 (GRCm39)	M2567L	unknown	Het
Cacna1e	T	A	1: 154,355,064 (GRCm39)	Y693F	possibly damaging	Het
Catsperg1	G	C	7: 28,884,152 (GRCm39)	T987R	probably damaging	Het
Cpa4	G	T	6: 30,574,393 (GRCm39)	D61Y	possibly damaging	Het
Cpne1	A	C	2: 155,921,080 (GRCm39)	V70G	probably damaging	Het
Dnase1l3	A	T	14: 7,987,306 (GRCm38)	N81K	probably damaging	Het
Duxf3	GCCC	GCC	10: 58,066,944 (GRCm39)		probably null	Het
Fbxo31	G	A	8: 122,281,136 (GRCm39)	R337C	probably damaging	Het
Fbxo34	C	G	14: 47,767,928 (GRCm39)	H480Q	probably benign	Het
Frmd4b	T	C	6: 97,398,559 (GRCm39)	E96G		Het
Gdpgp1	T	A	7: 79,888,216 (GRCm39)	D82E	probably benign	Het
Gjb3	GCCAGATGCGCCCA	GCCAGATGCGCCCAGATGCGCCCA	4: 127,220,458 (GRCm39)		probably null	Het
Grpel1	A	G	5: 36,626,823 (GRCm39)	N35S	probably benign	Het
Il12rb1	A	G	8: 71,273,291 (GRCm39)	T665A	possibly damaging	Het
Il16	T	C	7: 83,301,559 (GRCm39)	T886A	probably benign	Het
Insig1	T	A	5: 28,278,570 (GRCm39)	C128*	probably null	Het
Kcnk10	T	A	12: 98,484,775 (GRCm39)	E120D	probably benign	Het
Kctd1	T	C	18: 15,195,369 (GRCm39)	N418S	possibly damaging	Het
Kifbp	A	G	10: 62,395,037 (GRCm39)	V535A	probably damaging	Het
Klhl20	T	A	1: 160,933,055 (GRCm39)	H251L	probably damaging	Het
Ldlrad3	T	C	2: 101,888,326 (GRCm39)	D127G	probably damaging	Het
Lrp3	T	C	7: 34,903,182 (GRCm39)	Y388C	probably damaging	Het
Lrrc4	G	A	6: 28,830,206 (GRCm39)	R47W	possibly damaging	Het
Luzp1	A	T	4: 136,272,562 (GRCm39)	D1022V	probably damaging	Het
Mllt1	C	A	17: 57,212,737 (GRCm39)	R132L	probably damaging	Het
Ncoa1	G	T	12: 4,345,494 (GRCm39)	H618N	possibly damaging	Het
Nelfcd	T	C	2: 174,265,861 (GRCm39)	S318P	probably damaging	Het
Ngly1	A	C	14: 16,280,721 (GRCm38)	T301P	probably damaging	Het
Npy5r	G	A	8: 67,133,560 (GRCm39)	T411I	probably damaging	Het
Or55b10	T	C	7: 102,143,568 (GRCm39)	E138G	possibly damaging	Het
Or5d46	A	G	2: 88,170,248 (GRCm39)	N113S	probably benign	Het
Pcdha6	T	A	18: 37,101,593 (GRCm39)	I262N	probably damaging	Het
Pm20d1	C	A	1: 131,730,481 (GRCm39)	A245D	possibly damaging	Het
Rars1	T	C	11: 35,718,182 (GRCm39)		probably benign	Het
Rbms2	T	A	10: 127,987,107 (GRCm39)	I62F	probably damaging	Het
Rev3l	A	T	10: 39,700,809 (GRCm39)	T1769S	probably benign	Het
Rexo1	A	G	10: 80,378,854 (GRCm39)	Y1061H	probably damaging	Het
Rgs3	A	T	4: 62,500,240 (GRCm39)	I26F	probably damaging	Het
Rsf1	G	GACGGCGGCC	7: 97,229,116 (GRCm39)		probably benign	Het
Rtkn	A	T	6: 83,128,018 (GRCm39)	N406Y	possibly damaging	Het
Rtn4r	A	T	16: 17,969,708 (GRCm39)	I379F	possibly damaging	Het
Sez6	G	A	11: 77,865,121 (GRCm39)	E623K	possibly damaging	Het
Slmap	T	C	14: 26,137,355 (GRCm39)		probably benign	Het
Sorl1	A	T	9: 41,975,050 (GRCm39)	N519K	possibly damaging	Het
Srebf2	A	T	15: 82,056,975 (GRCm39)	I237F	possibly damaging	Het
Szt2	T	C	4: 118,242,651 (GRCm39)	S1479G	possibly damaging	Het
Tbc1d24	C	A	17: 24,400,274 (GRCm39)	E537*	probably null	Het
Ttf1	T	A	2: 28,957,080 (GRCm39)	I450K	probably benign	Het
Ube2e2	A	G	14: 18,893,288 (GRCm38)	S2P	unknown	Het
Utp20	T	C	10: 88,611,180 (GRCm39)	N1379S	probably damaging	Het
Vmn2r25	C	T	6: 123,805,391 (GRCm39)	V489I	probably benign	Het
Wfdc8	C	T	2: 164,439,245 (GRCm39)	R379H	unknown	Het
Zeb2	C	T	2: 45,003,136 (GRCm39)		probably benign	Het
Zfp3	C	T	11: 70,663,241 (GRCm39)	T400I	probably benign	Het
Zfp760	T	C	17: 21,941,932 (GRCm39)	I369T	possibly 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
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
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
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'- ACAGGGTGGTAAATTCTGAATCC -3'

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

Posted On

2021-12-30