Mutagenetix > Incidental Mutation

Incidental Mutation 'R8338:Peg10'

644731

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

067730-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8338 (G1)

Quality Score

121.467

Status

Not validated

Chromosome

Chromosomal Location

4747306-4760517 bp(+) (GRCm38)

Type of Mutation

small deletion (18 aa in frame mutation)

DNA Base Change (assembly)

CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG to CCACATCAGGATCCACATCAGGATGCACATCAG at 4756398 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: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ache	T	C	5: 137,291,744 (GRCm38)	L445P	probably damaging	Het
Agrn	G	A	4: 156,168,561 (GRCm38)	T1773I	probably benign	Het
Arap3	A	G	18: 37,973,630 (GRCm38)	S1387P	probably damaging	Het
Bcl11a	G	C	11: 24,164,578 (GRCm38)	K640N	probably damaging	Het
Bicd1	G	A	6: 149,513,123 (GRCm38)	V445I	probably benign	Het
Bltp3a	A	G	17: 27,876,695 (GRCm38)	N26S	probably damaging	Het
C2cd6	A	C	1: 59,060,575 (GRCm38)	N402K	probably benign	Het
Celsr3	C	T	9: 108,827,340 (GRCm38)	Q341*	probably null	Het
Cers1	A	G	8: 70,331,122 (GRCm38)	E240G	possibly damaging	Het
Cfap157	G	T	2: 32,778,006 (GRCm38)	T441N	possibly damaging	Het
Cfap44	G	A	16: 44,419,335 (GRCm38)		probably null	Het
Chd1	A	G	17: 15,769,980 (GRCm38)	Y1598C	probably damaging	Het
Ckap2l	T	G	2: 129,285,019 (GRCm38)	Q413P	probably damaging	Het
Cobl	T	C	11: 12,253,696 (GRCm38)	E1002G	probably benign	Het
Cryge	G	A	1: 65,048,774 (GRCm38)	T156M	unknown	Het
Cubn	A	C	2: 13,430,847 (GRCm38)	F1099L	probably benign	Het
Cyp7b1	T	C	3: 18,097,566 (GRCm38)	E161G	probably benign	Het
Dnah10	A	G	5: 124,832,502 (GRCm38)	E4452G	probably damaging	Het
Dnah2	C	T	11: 69,487,296 (GRCm38)	R1273Q	probably damaging	Het
Dnah3	T	C	7: 120,071,881 (GRCm38)	E593G	probably benign	Het
Dnah9	C	A	11: 65,841,241 (GRCm38)		probably null	Het
Dnajc22	C	A	15: 99,101,141 (GRCm38)	P69Q	probably benign	Het
Fam171a2	T	A	11: 102,438,346 (GRCm38)	D529V	probably benign	Het
Fbxl17	T	C	17: 63,356,758 (GRCm38)	I579V	possibly damaging	Het
Fry	C	T	5: 150,359,051 (GRCm38)	T347M	probably damaging	Het
Gm13272	A	C	4: 88,780,127 (GRCm38)	D93A	probably benign	Het
Grm4	A	T	17: 27,435,003 (GRCm38)	F658I	probably damaging	Het
Hmcn1	G	A	1: 150,738,734 (GRCm38)	T1307I	probably benign	Het
Igkv12-98	G	A	6: 68,571,175 (GRCm38)	S96N	probably benign	Het
Il2ra	A	T	2: 11,683,074 (GRCm38)	T222S	probably benign	Het
Il5ra	G	T	6: 106,712,389 (GRCm38)	T414K	probably benign	Het
Isg15	T	A	4: 156,199,631 (GRCm38)	I147F	probably benign	Het
Kif14	C	A	1: 136,494,678 (GRCm38)	A902E	probably damaging	Het
Lcat	G	A	8: 105,940,087 (GRCm38)	R268C	probably damaging	Het
Lipa	T	C	19: 34,494,077 (GRCm38)	N366S	probably benign	Het
Lrp4	A	G	2: 91,492,368 (GRCm38)	T1101A	probably benign	Het
Man1a	T	A	10: 53,925,547 (GRCm38)		probably null	Het
Mib1	A	G	18: 10,726,372 (GRCm38)	D23G	probably benign	Het
Morc2b	A	T	17: 33,136,413 (GRCm38)	M795K	probably benign	Het
Msantd5f1	T	A	4: 73,687,198 (GRCm38)	M282K	possibly damaging	Het
Mycbp2	T	A	14: 103,135,265 (GRCm38)	E4048D	probably damaging	Het
Myo7b	A	G	18: 31,971,355 (GRCm38)	S1447P	probably damaging	Het
Myt1	A	T	2: 181,801,862 (GRCm38)	T536S	possibly damaging	Het
Nod1	A	T	6: 54,943,971 (GRCm38)	L454Q	probably damaging	Het
Nrf1	T	A	6: 30,140,248 (GRCm38)	W199R		Het
Or10w1	T	A	19: 13,654,852 (GRCm38)	M141K	possibly damaging	Het
Or13a27	T	A	7: 140,345,393 (GRCm38)	M199L	probably benign	Het
Or14c44	T	C	7: 86,412,494 (GRCm38)	I44T	probably benign	Het
Or8k27	A	T	2: 86,445,385 (GRCm38)	M199K	probably benign	Het
Or9a4	T	C	6: 40,571,976 (GRCm38)	F197L	probably benign	Het
Ostn	G	T	16: 27,324,535 (GRCm38)	A38S	probably benign	Het
Paxbp1	A	T	16: 91,036,547 (GRCm38)	D266E	probably damaging	Het
Pcdhb14	G	T	18: 37,449,122 (GRCm38)	G427V	probably damaging	Het
Pdzrn3	A	T	6: 101,150,822 (GRCm38)	M961K	probably benign	Het
Prdx5	T	C	19: 6,907,264 (GRCm38)	D148G	probably damaging	Het
Ptprj	A	T	2: 90,471,137 (GRCm38)	I217N	possibly damaging	Het
Rccd1	A	T	7: 80,320,870 (GRCm38)	L54Q	possibly damaging	Het
Rfx6	T	A	10: 51,718,094 (GRCm38)	V370E	probably damaging	Het
Sdr16c6	C	T	4: 4,076,620 (GRCm38)	C93Y	probably damaging	Het
Shroom1	A	G	11: 53,463,280 (GRCm38)	D9G	probably benign	Het
Snrpe	A	G	1: 133,608,943 (GRCm38)	V33A	probably benign	Het
Spats2	T	A	15: 99,178,459 (GRCm38)	D139E	probably damaging	Het
Spopfm1	A	G	3: 94,265,978 (GRCm38)	I94V	possibly damaging	Het
St18	A	G	1: 6,809,292 (GRCm38)	E405G	probably damaging	Het
Strap	A	T	6: 137,741,978 (GRCm38)	E176V	possibly damaging	Het
Stxbp5l	G	T	16: 37,174,356 (GRCm38)	T729K	probably damaging	Het
Synj2bp	G	A	12: 81,504,552 (GRCm38)	Q97*	probably null	Het
Tbc1d32	T	A	10: 56,028,077 (GRCm38)	Q1198L	possibly damaging	Het
Tmem98	T	C	11: 80,821,309 (GRCm38)	S191P	probably benign	Het
Tnn	C	T	1: 160,118,483 (GRCm38)	G922R	probably damaging	Het
Treh	A	G	9: 44,684,511 (GRCm38)	N366S	probably benign	Het
Ttn	T	G	2: 76,919,792 (GRCm38)	S3638R	probably benign	Het
Uggt1	A	G	1: 36,227,521 (GRCm38)	L124P	probably damaging	Het
V1rd19	A	T	7: 24,003,249 (GRCm38)	K47*	probably null	Het
Wdhd1	T	C	14: 47,268,663 (GRCm38)	M265V	probably benign	Het
Wsb1	T	C	11: 79,246,277 (GRCm38)	D168G	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
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
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'- GTTTACAGTGCCACAACCG -3'
(R):5'- CCAGCCATGTGGTAGAAGAATG -3'

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

Posted On

2020-09-02