Mutagenetix > Incidental Mutation

Incidental Mutation 'R7475:Peg10'

579405

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

045549-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7475 (G1)

Quality Score

142.467

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: 100.0%
10x: 99.7%
20x: 98.9%

Validation Efficiency

99% (77/78)

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc5	G	T	16: 20,399,989	N214K	probably benign	Het
Abcf1	A	G	17: 35,963,567		probably null	Het
Agxt2	A	T	15: 10,409,537	M508L	probably benign	Het
Akr1c21	A	T	13: 4,576,319	Y114F	probably benign	Het
Amz1	T	C	5: 140,744,186		probably null	Het
Ank1	G	T	8: 23,132,630	A1732S	probably benign	Het
Atg16l1	T	C	1: 87,760,083	S50P	possibly damaging	Het
AW551984	A	G	9: 39,597,940	S302P	probably damaging	Het
Ces3a	T	A	8: 105,053,690		probably null	Het
Dedd	C	A	1: 171,340,313	P185Q	probably benign	Het
Fam186a	A	T	15: 99,947,514	V283E	unknown	Het
Fat2	C	A	11: 55,303,653	V1187F	probably benign	Het
Fbxw11	T	C	11: 32,711,999		probably null	Het
Fcgbp	C	T	7: 28,102,976	T1443I	probably damaging	Het
Foxj2	A	G	6: 122,837,842	D279G	probably benign	Het
Gbp5	A	G	3: 142,501,361	D97G	probably damaging	Het
Gm49368	A	T	7: 128,107,982	T661S	possibly damaging	Het
Gria4	T	G	9: 4,513,330	T260P	probably damaging	Het
Gtf2ird2	T	A	5: 134,201,426	D195E	possibly damaging	Het
Hectd4	T	A	5: 121,358,133		probably null	Het
Ifngr2	G	A	16: 91,557,909	C32Y	unknown	Het
Ikzf5	A	T	7: 131,392,059	C280S	probably benign	Het
Ints9	G	T	14: 65,026,465	E395D	probably null	Het
Isoc2b	T	C	7: 4,851,085	D96G	probably benign	Het
Jmjd1c	T	G	10: 67,225,313	S967R	probably benign	Het
Kcnj3	A	T	2: 55,437,326	K42N	probably benign	Het
Kiz	T	C	2: 146,891,086	V394A	possibly damaging	Het
Knl1	A	T	2: 119,087,546	H1795L	probably damaging	Het
Lmntd2	A	G	7: 141,210,689		probably null	Het
Loxhd1	C	A	18: 77,412,305	D1690E	possibly damaging	Het
Lrp1b	T	C	2: 41,344,576	D1121G		Het
Map3k2	T	C	18: 32,199,962	V63A	possibly damaging	Het
Mcc	G	T	18: 44,476,236	A499D	probably damaging	Het
Mcpt9	T	A	14: 56,026,943	I232F	probably damaging	Het
Meltf	A	G	16: 31,881,938	K92R	probably benign	Het
Mff	T	A	1: 82,745,438		probably null	Het
Mrgpra3	T	A	7: 47,589,947	Y77F	probably damaging	Het
Mylk	G	A	16: 34,914,076		probably null	Het
Ndufv2	A	G	17: 66,087,537	V111A	possibly damaging	Het
Nkd2	T	C	13: 73,825,742	E99G	probably damaging	Het
Nlk	C	A	11: 78,583,399	G358V	probably damaging	Het
Nnmt	A	T	9: 48,592,232	C165S	probably damaging	Het
Nxpe4	T	A	9: 48,393,340	C242*	probably null	Het
Oas1b	A	T	5: 120,817,640	N162I	probably damaging	Het
Olfr1191-ps1	A	G	2: 88,643,210	I148V	probably benign	Het
Otog	A	G	7: 46,267,276	N879S	probably damaging	Het
Park2	A	G	17: 11,434,614	D199G	probably benign	Het
Pcsk7	T	A	9: 45,927,625	Y612N	probably damaging	Het
Pgbd5	T	C	8: 124,434,011	D39G	probably benign	Het
Pkhd1l1	C	T	15: 44,505,185	Q800*	probably null	Het
Pkn3	T	C	2: 30,087,110	S621P	probably benign	Het
Polr3c	T	C	3: 96,715,185	I385V	probably benign	Het
Ppp1r21	G	T	17: 88,555,603	G257W	probably benign	Het
Pxylp1	C	T	9: 96,856,367		probably null	Het
Rasgrp1	T	C	2: 117,286,108	T613A	probably benign	Het
Robo3	C	T	9: 37,425,378	V387I	probably benign	Het
Rxfp2	T	A	5: 150,049,581	Y174N	possibly damaging	Het
Sec24a	T	C	11: 51,713,552	M746V	probably damaging	Het
Sema4f	T	A	6: 82,914,374	E571D	possibly damaging	Het
Sept3	T	C	15: 82,286,456	V217A	probably benign	Het
Serpinb1b	A	C	13: 33,093,565	K260N	probably benign	Het
Sin3b	A	G	8: 72,749,872	T645A	possibly damaging	Het
Sobp	C	T	10: 43,021,834	R585Q	probably damaging	Het
Specc1l	T	A	10: 75,246,447	L559Q	possibly damaging	Het
Srxn1	C	T	2: 152,105,653		probably benign	Het
Sspo	G	A	6: 48,455,860	R890Q	probably benign	Het
Stard9	A	G	2: 120,688,110	D505G	probably damaging	Het
Tjp1	A	T	7: 65,322,339	I653K	probably damaging	Het
Tnks	C	T	8: 34,831,712	E1296K	probably damaging	Het
Ttbk2	A	T	2: 120,748,640	I667N	probably benign	Het
Usp24	T	C	4: 106,342,353	S165P	possibly damaging	Het
Usp46	T	A	5: 74,028,937	K109*	probably null	Het
Vmn1r191	A	G	13: 22,178,772	C271R	probably benign	Het
Wisp3	T	A	10: 39,158,300	Y102F	probably damaging	Het
Zfp592	T	C	7: 81,023,452	S55P	probably damaging	Het
Zmynd15	T	C	11: 70,461,041	S158P	probably benign	Het
Zscan22	T	G	7: 12,906,737	C303G	probably damaging	Het

Other mutations in Peg10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02029:Peg10	APN	6	4754473	utr 5 prime	probably benign
IGL03063:Peg10	APN	6	4756647	utr 3 prime	probably benign
piaggio	UTSW	6	4756427	utr 3 prime	probably benign
PIT4480001:Peg10	UTSW	6	4756560	missense	unknown
R0090:Peg10	UTSW	6	4756063	utr 3 prime	probably benign
R0148:Peg10	UTSW	6	4755711	missense	possibly damaging	0.88
R0650:Peg10	UTSW	6	4756475	small insertion	probably benign
R0698:Peg10	UTSW	6	4756835	utr 3 prime	probably benign
R1600:Peg10	UTSW	6	4757080	utr 3 prime	probably benign
R1842:Peg10	UTSW	6	4756381	utr 3 prime	probably benign
R1930:Peg10	UTSW	6	4755778	missense	probably damaging	0.99
R1931:Peg10	UTSW	6	4755778	missense	probably damaging	0.99
R2162:Peg10	UTSW	6	4755914	utr 3 prime	probably benign
R2215:Peg10	UTSW	6	4756918	utr 3 prime	probably benign
R2339:Peg10	UTSW	6	4756102	utr 3 prime	probably benign
R2847:Peg10	UTSW	6	4756912	utr 3 prime	probably benign
R2848:Peg10	UTSW	6	4756912	utr 3 prime	probably benign
R3000:Peg10	UTSW	6	4754276	utr 5 prime	probably benign
R3056:Peg10	UTSW	6	4755029	missense	possibly damaging	0.66
R4051:Peg10	UTSW	6	4754534	missense	probably benign	0.00
R4059:Peg10	UTSW	6	4756427	utr 3 prime	probably benign
R4296:Peg10	UTSW	6	4756472	small insertion	probably benign
R4626:Peg10	UTSW	6	4756460	small insertion	probably benign
R4634:Peg10	UTSW	6	4756452	small insertion	probably benign
R4679:Peg10	UTSW	6	4756452	small insertion	probably benign
R4834:Peg10	UTSW	6	4754294	utr 5 prime	probably benign
R4982:Peg10	UTSW	6	4756451	small insertion	probably benign
R4983:Peg10	UTSW	6	4756451	small insertion	probably benign
R4996:Peg10	UTSW	6	4756454	small insertion	probably benign
R4997:Peg10	UTSW	6	4756457	small insertion	probably benign
R5015:Peg10	UTSW	6	4756453	small insertion	probably benign
R5085:Peg10	UTSW	6	4755864	utr 3 prime	probably benign
R5091:Peg10	UTSW	6	4754511	missense	probably benign	0.01
R5231:Peg10	UTSW	6	4756939	utr 3 prime	probably benign
R5278:Peg10	UTSW	6	4756442	small deletion	probably benign
R5364:Peg10	UTSW	6	4756128	utr 3 prime	probably benign
R5397:Peg10	UTSW	6	4756453	small insertion	probably benign
R5485:Peg10	UTSW	6	4755565	missense	probably benign	0.09
R5573:Peg10	UTSW	6	4755913	utr 3 prime	probably benign
R5710:Peg10	UTSW	6	4756350	small insertion	probably benign
R5710:Peg10	UTSW	6	4756351	small insertion	probably benign
R5736:Peg10	UTSW	6	4754423	missense	probably benign	0.00
R5865:Peg10	UTSW	6	4754375	missense	probably damaging	0.98
R6056:Peg10	UTSW	6	4756449	small insertion	probably benign
R6116:Peg10	UTSW	6	4756351	small insertion	probably benign
R6129:Peg10	UTSW	6	4756449	small insertion	probably benign
R6147:Peg10	UTSW	6	4754499	start gained	probably benign
R6171:Peg10	UTSW	6	4756449	small insertion	probably benign
R6194:Peg10	UTSW	6	4756351	small insertion	probably benign
R6197:Peg10	UTSW	6	4756452	small insertion	probably benign
R6207:Peg10	UTSW	6	4756449	small insertion	probably benign
R6215:Peg10	UTSW	6	4756452	small insertion	probably benign
R6276:Peg10	UTSW	6	4756449	small insertion	probably benign
R6281:Peg10	UTSW	6	4756449	small insertion	probably benign
R6287:Peg10	UTSW	6	4756451	small insertion	probably benign
R6302:Peg10	UTSW	6	4756449	small insertion	probably benign
R6393:Peg10	UTSW	6	4756452	small insertion	probably benign
R6394:Peg10	UTSW	6	4756451	small insertion	probably benign
R6405:Peg10	UTSW	6	4756453	small insertion	probably benign
R6421:Peg10	UTSW	6	4756449	small insertion	probably benign
R6486:Peg10	UTSW	6	4756449	small insertion	probably benign
R6538:Peg10	UTSW	6	4756449	small insertion	probably benign
R6668:Peg10	UTSW	6	4754502	missense	probably benign	0.01
R6679:Peg10	UTSW	6	4754276	utr 5 prime	probably benign
R6685:Peg10	UTSW	6	4754738	missense	probably damaging	1.00
R6702:Peg10	UTSW	6	4756452	small insertion	probably benign
R6706:Peg10	UTSW	6	4756452	small insertion	probably benign
R6747:Peg10	UTSW	6	4757137	utr 3 prime	probably benign
R6775:Peg10	UTSW	6	4756452	small insertion	probably benign
R6811:Peg10	UTSW	6	4756451	small insertion	probably benign
R6823:Peg10	UTSW	6	4756431	small deletion	probably benign
R6826:Peg10	UTSW	6	4756353	small insertion	probably benign
R6847:Peg10	UTSW	6	4754279	utr 5 prime	probably benign
R6861:Peg10	UTSW	6	4756350	small insertion	probably benign
R6861:Peg10	UTSW	6	4756351	small insertion	probably benign
R6876:Peg10	UTSW	6	4756451	small insertion	probably benign
R6891:Peg10	UTSW	6	4756449	small insertion	probably benign
R6911:Peg10	UTSW	6	4756452	small insertion	probably benign
R6973:Peg10	UTSW	6	4756431	small deletion	probably benign
R6990:Peg10	UTSW	6	4756451	small insertion	probably benign
R6998:Peg10	UTSW	6	4756398	small deletion	probably benign
R7070:Peg10	UTSW	6	4756454	small insertion	probably benign
R7120:Peg10	UTSW	6	4756398	small deletion	probably benign
R7132:Peg10	UTSW	6	4756398	small deletion	probably benign
R7140:Peg10	UTSW	6	4756452	small insertion	probably benign
R7189:Peg10	UTSW	6	4756431	small deletion	probably benign
R7208:Peg10	UTSW	6	4756398	small deletion	probably benign
R7256:Peg10	UTSW	6	4756398	small deletion	probably benign
R7260:Peg10	UTSW	6	4756398	small deletion	probably benign
R7261:Peg10	UTSW	6	4756591	missense	unknown
R7401:Peg10	UTSW	6	4756452	small insertion	probably benign
R7409:Peg10	UTSW	6	4756398	small deletion	probably benign
R7439:Peg10	UTSW	6	4756453	small insertion	probably benign
R7483:Peg10	UTSW	6	4756451	small insertion	probably benign
R7502:Peg10	UTSW	6	4756398	small deletion	probably benign
R7515:Peg10	UTSW	6	4756452	small insertion	probably benign
R7520:Peg10	UTSW	6	4756796	missense	unknown
R7544:Peg10	UTSW	6	4756427	frame shift	probably null
R7571:Peg10	UTSW	6	4756082	missense	unknown
R7581:Peg10	UTSW	6	4756452	small insertion	probably benign
R7635:Peg10	UTSW	6	4754938	missense	probably damaging	0.99
R7677:Peg10	UTSW	6	4756398	small deletion	probably benign
R7697:Peg10	UTSW	6	4756453	small insertion	probably benign
R7710:Peg10	UTSW	6	4756452	small insertion	probably benign
R7803:Peg10	UTSW	6	4756431	small deletion	probably benign
R7816:Peg10	UTSW	6	4756453	small insertion	probably benign
R7820:Peg10	UTSW	6	4756398	small deletion	probably benign
R7827:Peg10	UTSW	6	4756452	small insertion	probably benign
R7861:Peg10	UTSW	6	4756431	small deletion	probably benign
R7881:Peg10	UTSW	6	4756454	small insertion	probably benign
R7904:Peg10	UTSW	6	4756452	small insertion	probably benign
R7915:Peg10	UTSW	6	4756451	small insertion	probably benign
R7916:Peg10	UTSW	6	4756451	small insertion	probably benign
R7963:Peg10	UTSW	6	4756452	small insertion	probably benign
R8016:Peg10	UTSW	6	4756451	small insertion	probably benign
R8037:Peg10	UTSW	6	4756398	small deletion	probably benign
R8062:Peg10	UTSW	6	4756398	small deletion	probably benign
R8081:Peg10	UTSW	6	4756452	small insertion	probably benign
R8113:Peg10	UTSW	6	4756451	small insertion	probably benign
R8115:Peg10	UTSW	6	4756707	missense	unknown
R8140:Peg10	UTSW	6	4756113	missense	unknown
R8178:Peg10	UTSW	6	4756452	small insertion	probably benign
R8233:Peg10	UTSW	6	4756453	small insertion	probably benign
R8239:Peg10	UTSW	6	4756452	small insertion	probably benign
R8281:Peg10	UTSW	6	4756431	small deletion	probably benign
R8310:Peg10	UTSW	6	4756454	small insertion	probably benign
R8312:Peg10	UTSW	6	4756452	small insertion	probably benign
R8330:Peg10	UTSW	6	4756452	small insertion	probably benign
R8338:Peg10	UTSW	6	4756398	small deletion	probably benign
R8354:Peg10	UTSW	6	4756452	small insertion	probably benign
R8387:Peg10	UTSW	6	4756452	small insertion	probably benign
R8390:Peg10	UTSW	6	4756451	small insertion	probably benign
R8408:Peg10	UTSW	6	4756453	small insertion	probably benign
R8415:Peg10	UTSW	6	4756451	small insertion	probably benign
R8439:Peg10	UTSW	6	4755462	missense	possibly damaging	0.58
R8444:Peg10	UTSW	6	4756398	small deletion	probably benign
R8463:Peg10	UTSW	6	4756453	small insertion	probably benign
R8477:Peg10	UTSW	6	4756453	small insertion	probably benign
R8507:Peg10	UTSW	6	4756453	small insertion	probably benign
R8552:Peg10	UTSW	6	4756452	small insertion	probably benign
R8678:Peg10	UTSW	6	4756431	small deletion	probably benign
R8699:Peg10	UTSW	6	4756451	small insertion	probably benign
R8700:Peg10	UTSW	6	4756451	small insertion	probably benign
R8705:Peg10	UTSW	6	4756398	small deletion	probably benign
R8765:Peg10	UTSW	6	4754492	missense	unknown
R8824:Peg10	UTSW	6	4756451	small insertion	probably benign
R8859:Peg10	UTSW	6	4756451	small insertion	probably benign
R8870:Peg10	UTSW	6	4754825	missense	probably damaging	0.99
R8909:Peg10	UTSW	6	4756451	small insertion	probably benign
R8918:Peg10	UTSW	6	4756398	small deletion	probably benign
R8924:Peg10	UTSW	6	4756398	small deletion	probably benign
R8925:Peg10	UTSW	6	4756452	small insertion	probably benign
R8930:Peg10	UTSW	6	4756449	small insertion	probably benign
R8950:Peg10	UTSW	6	4756452	small insertion	probably benign
R8960:Peg10	UTSW	6	4756449	small insertion	probably benign
R8975:Peg10	UTSW	6	4756452	small insertion	probably benign
R8988:Peg10	UTSW	6	4756398	small deletion	probably benign
R9046:Peg10	UTSW	6	4756452	small insertion	probably benign
R9068:Peg10	UTSW	6	4756451	small insertion	probably benign
R9074:Peg10	UTSW	6	4756451	small insertion	probably benign
R9088:Peg10	UTSW	6	4756453	small insertion	probably benign
R9094:Peg10	UTSW	6	4756449	small insertion	probably benign
R9114:Peg10	UTSW	6	4756452	small insertion	probably benign
R9116:Peg10	UTSW	6	4756452	small insertion	probably benign
R9135:Peg10	UTSW	6	4756453	small insertion	probably benign
R9137:Peg10	UTSW	6	4756398	small deletion	probably benign
R9139:Peg10	UTSW	6	4756449	small insertion	probably benign
R9139:Peg10	UTSW	6	4757128	missense	unknown
R9171:Peg10	UTSW	6	4756452	small insertion	probably benign
R9173:Peg10	UTSW	6	4756451	small insertion	probably benign
R9213:Peg10	UTSW	6	4756451	small insertion	probably benign
R9216:Peg10	UTSW	6	4756452	small insertion	probably benign
R9229:Peg10	UTSW	6	4756398	small deletion	probably benign
R9233:Peg10	UTSW	6	4756398	small deletion	probably benign
R9283:Peg10	UTSW	6	4756452	small insertion	probably benign
R9328:Peg10	UTSW	6	4756398	small deletion	probably benign
R9367:Peg10	UTSW	6	4756398	small deletion	probably benign
R9369:Peg10	UTSW	6	4756452	small insertion	probably benign
R9405:Peg10	UTSW	6	4756398	small deletion	probably benign
R9410:Peg10	UTSW	6	4756452	small insertion	probably benign
R9412:Peg10	UTSW	6	4756453	small insertion	probably benign
R9421:Peg10	UTSW	6	4756398	small deletion	probably benign
R9437:Peg10	UTSW	6	4756451	small insertion	probably benign
R9440:Peg10	UTSW	6	4756451	small insertion	probably benign
R9460:Peg10	UTSW	6	4756452	small insertion	probably benign
R9492:Peg10	UTSW	6	4756398	small deletion	probably benign
R9495:Peg10	UTSW	6	4756451	small insertion	probably benign
R9500:Peg10	UTSW	6	4756871	missense	unknown
R9511:Peg10	UTSW	6	4756451	small insertion	probably benign
R9515:Peg10	UTSW	6	4756452	small insertion	probably benign
R9576:Peg10	UTSW	6	4756398	small deletion	probably benign
R9610:Peg10	UTSW	6	4756452	small insertion	probably benign
R9611:Peg10	UTSW	6	4756452	small insertion	probably benign
R9611:Peg10	UTSW	6	4756453	small insertion	probably benign
R9614:Peg10	UTSW	6	4756451	small insertion	probably benign
R9619:Peg10	UTSW	6	4755316	missense	probably benign	0.02
R9646:Peg10	UTSW	6	4756452	small insertion	probably benign
R9655:Peg10	UTSW	6	4756398	small deletion	probably benign
R9673:Peg10	UTSW	6	4756452	small insertion	probably benign
R9675:Peg10	UTSW	6	4756398	small deletion	probably benign
R9696:Peg10	UTSW	6	4756431	small deletion	probably benign
R9749:Peg10	UTSW	6	4756398	small deletion	probably benign
R9756:Peg10	UTSW	6	4756452	small insertion	probably benign
X0065:Peg10	UTSW	6	4756515	utr 3 prime	probably benign
Z1176:Peg10	UTSW	6	4756451	small insertion	probably benign

Predicted Primers

PCR Primer
(F):5'- CTGTTTACAGTGCCACAACCG -3'
(R):5'- TAGAAGAATGGTGGCTGCTG -3'

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

Posted On

2019-10-07