Mutagenetix > Incidental Mutation

Incidental Mutation 'R9696:Peg10'

729281

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

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9696 (G1)

Quality Score

148.467

Status

Not validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm39)

Type of Mutation

small deletion (18 aa in frame mutation)

DNA Base Change (assembly)

CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC to CATC at 4756431 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: 100.0%
3x: 99.9%
10x: 99.6%
20x: 99.0%

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: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001O22Rik	T	C	2: 30,691,256 (GRCm39)	D105G	possibly damaging	Het
4930407I10Rik	A	G	15: 81,949,697 (GRCm39)	N1198S	probably benign	Het
Abca14	A	T	7: 119,888,734 (GRCm39)	I1227F	possibly damaging	Het
Abhd10	T	C	16: 45,552,042 (GRCm39)	D277G	probably damaging	Het
Adam20	A	G	8: 41,249,633 (GRCm39)	N581S	probably damaging	Het
Apbb1ip	A	T	2: 22,725,989 (GRCm39)	T254S	probably benign	Het
Arap3	T	C	18: 38,112,905 (GRCm39)	T1102A	probably damaging	Het
Asb16	A	T	11: 102,159,766 (GRCm39)	R40W	probably damaging	Het
Birc6	T	A	17: 74,947,292 (GRCm39)	S3019T	probably damaging	Het
Btbd18	T	A	2: 84,497,854 (GRCm39)	C497*	probably null	Het
Cacna1h	T	C	17: 25,602,215 (GRCm39)	M1542V	possibly damaging	Het
Ccdc8	T	G	7: 16,730,087 (GRCm39)	S525R	unknown	Het
Ch25h	G	A	19: 34,451,947 (GRCm39)	R194W	probably damaging	Het
Ciapin1	C	A	8: 95,555,065 (GRCm39)	L130F	probably damaging	Het
Cnfn	G	T	7: 25,067,515 (GRCm39)	T54N	probably damaging	Het
Cop1	A	T	1: 159,076,783 (GRCm39)	I195F	probably damaging	Het
Daam1	A	G	12: 71,991,147 (GRCm39)	R254G	unknown	Het
Dcaf13	T	C	15: 39,001,496 (GRCm39)	M268T	possibly damaging	Het
Disp3	C	A	4: 148,345,611 (GRCm39)	V410L	probably damaging	Het
Dus4l	A	T	12: 31,696,647 (GRCm39)	I110K	probably damaging	Het
Endov	C	T	11: 119,398,048 (GRCm39)	P271L	probably damaging	Het
Epha2	A	G	4: 141,047,834 (GRCm39)	I539V	probably benign	Het
Ercc4	A	T	16: 12,950,810 (GRCm39)	I635L	probably damaging	Het
Exosc10	A	G	4: 148,649,704 (GRCm39)	D378G	probably damaging	Het
Fmnl1	A	G	11: 103,086,297 (GRCm39)	D804G	unknown	Het
Gm11983	T	A	11: 6,787,020 (GRCm39)	I36F	unknown	Het
Gm11992	A	T	11: 9,006,438 (GRCm39)	I123L	probably benign	Het
Gm19965	T	C	1: 116,730,838 (GRCm39)		probably benign	Het
Gm19965	A	G	1: 116,749,210 (GRCm39)	D297G		Het
Gpr180	G	A	14: 118,391,302 (GRCm39)	G235R	probably damaging	Het
Gse1	T	C	8: 120,956,280 (GRCm39)	V257A	unknown	Het
Haus1	A	T	18: 77,847,202 (GRCm39)	S225T	probably benign	Het
Hgf	A	G	5: 16,777,534 (GRCm39)	Y177C	probably damaging	Het
Insig1	T	C	5: 28,279,546 (GRCm39)	W184R	probably damaging	Het
Krt5	A	T	15: 101,616,141 (GRCm39)	S491R	unknown	Het
Lcn5	A	G	2: 25,550,142 (GRCm39)	I110V	probably benign	Het
Lin9	A	T	1: 180,496,733 (GRCm39)	S341C	possibly damaging	Het
Magi2	C	T	5: 20,670,864 (GRCm39)	H403Y	probably benign	Het
Mapk1ip1l	C	T	14: 47,548,340 (GRCm39)	P163S	probably damaging	Het
Mbtd1	A	G	11: 93,823,218 (GRCm39)	D568G	probably damaging	Het
Mdp1	A	G	14: 55,896,704 (GRCm39)	V119A	probably benign	Het
Me1	A	G	9: 86,469,047 (GRCm39)	I506T	probably damaging	Het
Med1	A	G	11: 98,061,772 (GRCm39)		probably null	Het
Med25	T	A	7: 44,529,524 (GRCm39)	Q656L	probably benign	Het
Memo1	A	C	17: 74,524,041 (GRCm39)	I213S	probably damaging	Het
Mfsd14b	C	A	13: 65,221,414 (GRCm39)	V293L	probably benign	Het
Mpi	T	C	9: 57,452,539 (GRCm39)	D331G	probably benign	Het
Muc4	T	C	16: 32,574,712 (GRCm39)	I1054T	probably benign	Het
Nat10	T	C	2: 103,556,040 (GRCm39)	E927G	possibly damaging	Het
Nlrp9a	T	C	7: 26,275,033 (GRCm39)	L930P	unknown	Het
Nt5c3b	A	T	11: 100,323,811 (GRCm39)	I167N	probably damaging	Het
Ogdh	T	C	11: 6,289,209 (GRCm39)	S308P	probably damaging	Het
Or2y1b	A	G	11: 49,208,390 (GRCm39)	I6V	probably benign	Het
Or4c108	T	G	2: 88,803,615 (GRCm39)	I207L	probably benign	Het
Or52e5	T	A	7: 104,719,283 (GRCm39)	V203D	probably damaging	Het
Or8b9	G	A	9: 37,766,671 (GRCm39)	E186K	probably benign	Het
Parl	A	G	16: 20,105,690 (GRCm39)	V244A	probably benign	Het
Parp14	G	T	16: 35,661,252 (GRCm39)	D1565E	probably damaging	Het
Parp14	T	C	16: 35,661,251 (GRCm39)	K1566E	possibly damaging	Het
Pcdhb18	T	A	18: 37,623,606 (GRCm39)	I312K	possibly damaging	Het
Pcnp	A	T	16: 55,844,867 (GRCm39)		probably benign	Het
Rab10	T	A	12: 3,306,947 (GRCm39)	M83L	probably benign	Het
Rabep1	A	G	11: 70,814,029 (GRCm39)	S616G	probably benign	Het
Rnf213	G	A	11: 119,359,806 (GRCm39)	V4400M		Het
Samd9l	T	A	6: 3,375,078 (GRCm39)	I728F	possibly damaging	Het
Scaf4	T	A	16: 90,044,122 (GRCm39)	D620V	unknown	Het
Scnn1b	A	T	7: 121,498,462 (GRCm39)	M1L	probably damaging	Het
Sec23b	T	A	2: 144,428,343 (GRCm39)	M652K	probably benign	Het
Selenoi	T	C	5: 30,453,413 (GRCm39)	F44L	probably benign	Het
Slc36a3	A	T	11: 55,026,161 (GRCm39)	V219E	possibly damaging	Het
Sncaip	A	T	18: 53,038,915 (GRCm39)	Q543L	probably damaging	Het
Stmnd1	A	G	13: 46,443,224 (GRCm39)	I119V	probably damaging	Het
Strn3	T	A	12: 51,676,286 (GRCm39)	E414D	probably damaging	Het
Syne1	T	A	10: 5,297,847 (GRCm39)	H1150L	probably benign	Het
Tdrd7	A	G	4: 46,016,888 (GRCm39)	N676S	possibly damaging	Het
Tgs1	A	T	4: 3,575,071 (GRCm39)	I16F	possibly damaging	Het
Thnsl2	T	G	6: 71,108,930 (GRCm39)	T294P	possibly damaging	Het
Tmem156	A	G	5: 65,231,147 (GRCm39)	I241T	possibly damaging	Het
Unc13a	A	T	8: 72,082,197 (GRCm39)	M1689K	possibly damaging	Het
Uri1	T	C	7: 37,664,738 (GRCm39)	D318G	probably benign	Het
Vmn2r86	T	A	10: 130,285,702 (GRCm39)	Q491L	possibly damaging	Het
Vps13b	C	A	15: 35,675,033 (GRCm39)	Q1718K	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
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
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'- TGTTTACAGTGCCACAACCG -3'
(R):5'- AATCCAGCCATGTGGTAGAAG -3'

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

Posted On

2022-10-06