Mutagenetix > Incidental Mutation

Incidental Mutation 'R1760:Exosc10'

192683

Institutional Source

Beutler Lab

Gene Symbol

Exosc10

Ensembl Gene

ENSMUSG00000017264

Gene Name

exosome component 10

Synonyms

PM-Scl, Pmscl2, p2, p3, p4, RRP6, PM/Scl-100

MMRRC Submission

039792-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.971) question?

Stock #

R1760 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

148642886-148666858 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 148662926 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 712 (K712*)

Ref Sequence

ENSEMBL: ENSMUSP00000075401 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000017408] [ENSMUST00000076022] [ENSMUST00000097781]

AlphaFold

P56960

Predicted Effect

probably null
Transcript: ENSMUST00000017408
AA Change: K737*

SMART Domains

Protein: ENSMUSP00000017408
Gene: ENSMUSG00000017264
AA Change: K737*

Domain	Start	End	E-Value	Type
Pfam:PMC2NT	44	133	2.7e-26	PFAM
low complexity region	219	230	N/A	INTRINSIC
35EXOc	288	456	7.84e-53	SMART
HRDC	503	583	8.24e-25	SMART
low complexity region	745	760	N/A	INTRINSIC
coiled coil region	769	800	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000076022
AA Change: K712*

SMART Domains

Protein: ENSMUSP00000075401
Gene: ENSMUSG00000017264
AA Change: K712*

Domain	Start	End	E-Value	Type
Pfam:PMC2NT	43	134	5.1e-30	PFAM
low complexity region	219	230	N/A	INTRINSIC
35EXOc	288	456	7.84e-53	SMART
HRDC	503	583	8.24e-25	SMART
low complexity region	720	735	N/A	INTRINSIC
coiled coil region	744	775	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000097781

SMART Domains

Protein: ENSMUSP00000095388
Gene: ENSMUSG00000017264

Domain	Start	End	E-Value	Type
Pfam:PMC2NT	43	134	1.4e-30	PFAM
low complexity region	219	230	N/A	INTRINSIC
35EXOc	288	456	7.84e-53	SMART
HRDC	503	583	8.24e-25	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126897

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173154

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173767

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173892

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.6%

Validation Efficiency

97% (95/98)

MGI Phenotype

PHENOTYPE: Mice homozygous for a conditional allele appear phenotypically normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 92 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca2	T	C	2: 25,333,055 (GRCm39)	S1585P	probably benign	Het
Abhd16b	T	C	2: 181,135,197 (GRCm39)	F33S	probably damaging	Het
Adgra2	G	A	8: 27,609,795 (GRCm39)	R856Q	probably damaging	Het
Aff3	A	T	1: 38,368,945 (GRCm39)		probably benign	Het
Anxa2	A	T	9: 69,397,049 (GRCm39)	Y251F	probably benign	Het
Arid1b	A	G	17: 5,392,088 (GRCm39)	T1873A	probably damaging	Het
Baz1b	C	A	5: 135,271,378 (GRCm39)	D1320E	probably benign	Het
Bbs1	A	T	19: 4,944,350 (GRCm39)	S426R	probably benign	Het
Bid	A	G	6: 120,877,209 (GRCm39)	V44A	possibly damaging	Het
Ccdc60	T	A	5: 116,310,532 (GRCm39)	M177L	probably damaging	Het
Cdh23	G	A	10: 60,161,855 (GRCm39)	T1997M	probably damaging	Het
Cdh5	T	A	8: 104,854,801 (GRCm39)	M243K	probably benign	Het
Clpb	T	A	7: 101,435,905 (GRCm39)	V578E	possibly damaging	Het
Cngb1	C	A	8: 96,026,328 (GRCm39)	C151F	probably benign	Het
Cntnap5b	T	C	1: 99,700,535 (GRCm39)	S16P	probably benign	Het
Cr1l	T	A	1: 194,797,123 (GRCm39)	M305L	probably benign	Het
Ctnnal1	A	T	4: 56,838,988 (GRCm39)	M235K	probably damaging	Het
Ddx55	A	T	5: 124,706,176 (GRCm39)	R534W	probably damaging	Het
Dip2b	T	A	15: 100,109,910 (GRCm39)	L1465Q	probably damaging	Het
Dnah9	G	T	11: 65,872,048 (GRCm39)	D2727E	probably benign	Het
Dph3b-ps	A	C	13: 106,683,497 (GRCm39)		noncoding transcript	Het
Dst	T	A	1: 34,267,684 (GRCm39)	L2702Q	probably damaging	Het
Efnb2	T	C	8: 8,673,184 (GRCm39)	T158A	possibly damaging	Het
Fgr	T	C	4: 132,725,653 (GRCm39)	V354A	possibly damaging	Het
Fsip2	A	G	2: 82,830,185 (GRCm39)	D6893G	possibly damaging	Het
Fsip2	G	A	2: 82,815,240 (GRCm39)	V3658M	probably benign	Het
Fsip2	A	T	2: 82,818,055 (GRCm39)	H4596L	possibly damaging	Het
Gm1527	G	A	3: 28,949,699 (GRCm39)		probably benign	Het
Gm5150	G	T	3: 16,060,468 (GRCm39)	Q7K	probably benign	Het
Gpr155	C	T	2: 73,212,279 (GRCm39)	V115M	probably damaging	Het
Gpr75	T	C	11: 30,841,527 (GRCm39)	L144P	probably damaging	Het
Gsn	T	A	2: 35,174,835 (GRCm39)	Y127N	probably damaging	Het
Hk1	A	G	10: 62,117,678 (GRCm39)	L615S	probably damaging	Het
Igsf9b	A	G	9: 27,229,123 (GRCm39)	T194A	possibly damaging	Het
Il17rd	C	T	14: 26,813,763 (GRCm39)	Q46*	probably null	Het
Jak1	T	A	4: 101,020,126 (GRCm39)	M678L	probably benign	Het
Kif6	T	C	17: 49,922,311 (GRCm39)	V16A	probably benign	Het
Kpna3	T	C	14: 61,607,990 (GRCm39)	E405G	probably benign	Het
Lmtk2	C	A	5: 144,110,993 (GRCm39)	T571K	probably damaging	Het
Mucl2	T	C	15: 103,927,838 (GRCm39)	T40A	possibly damaging	Het
Myh11	G	A	16: 14,051,559 (GRCm39)		probably benign	Het
Myh7	C	T	14: 55,210,170 (GRCm39)	R1845Q	probably damaging	Het
Myo1f	T	A	17: 33,805,172 (GRCm39)	L480Q	probably benign	Het
Nek9	T	G	12: 85,352,364 (GRCm39)	D833A	possibly damaging	Het
Nek9	T	C	12: 85,357,184 (GRCm39)	E660G	probably benign	Het
Or10z1	C	T	1: 174,077,926 (GRCm39)	C189Y	probably damaging	Het
Or2a12	A	G	6: 42,904,431 (GRCm39)	I89V	possibly damaging	Het
Or2t45	A	G	11: 58,669,195 (GRCm39)	M81V	possibly damaging	Het
Or5h18	T	C	16: 58,847,350 (GRCm39)	R307G	probably benign	Het
Or6c65	T	A	10: 129,603,417 (GRCm39)	D17E	probably benign	Het
Or6f2	G	A	7: 139,756,188 (GRCm39)	V52M	probably damaging	Het
Or7s1a-ps1	T	A	9: 18,843,791 (GRCm39)		probably benign	Het
Otud3	G	T	4: 138,623,092 (GRCm39)	T383K	possibly damaging	Het
Pkp4	T	C	2: 59,142,185 (GRCm39)	L496P	probably damaging	Het
Pla2g4e	C	A	2: 120,000,527 (GRCm39)	A737S	possibly damaging	Het
Pla2g4f	T	C	2: 120,144,547 (GRCm39)		probably benign	Het
Plxnd1	A	T	6: 115,944,740 (GRCm39)	V1018E	possibly damaging	Het
Ppp1r21	T	G	17: 88,869,653 (GRCm39)	V402G	possibly damaging	Het
Prkcq	T	G	2: 11,304,881 (GRCm39)	M690R	probably damaging	Het
Ptpra	T	C	2: 130,391,747 (GRCm39)	I719T	probably damaging	Het
Rab3ip	C	T	10: 116,773,415 (GRCm39)	D133N	probably damaging	Het
Relch	T	G	1: 105,647,169 (GRCm39)		probably benign	Het
Rsbn1	T	A	3: 103,867,347 (GRCm39)	Y563N	probably damaging	Het
Rtf1	A	C	2: 119,558,889 (GRCm39)	D530A	probably benign	Het
Rybp	G	T	6: 100,209,224 (GRCm39)	S199R	probably benign	Het
Sema5a	T	G	15: 32,641,252 (GRCm39)	C689G	probably damaging	Het
Senp6	T	A	9: 80,025,911 (GRCm39)	V314E	probably benign	Het
Setd1a	T	A	7: 127,385,062 (GRCm39)	C47S	possibly damaging	Het
Slamf1	C	A	1: 171,604,734 (GRCm39)	T168K	probably benign	Het
Slc12a5	T	C	2: 164,838,048 (GRCm39)	S937P	probably damaging	Het
Slc38a11	C	T	2: 65,185,663 (GRCm39)		probably null	Het
Slc6a2	C	T	8: 93,687,846 (GRCm39)		probably benign	Het
Snw1	A	T	12: 87,511,459 (GRCm39)	F64Y	probably benign	Het
Spata9	A	C	13: 76,146,643 (GRCm39)	I172L	probably benign	Het
Sphkap	T	C	1: 83,255,265 (GRCm39)	H828R	probably benign	Het
Spmip6	T	A	4: 41,507,330 (GRCm39)		probably null	Het
Tmem94	A	T	11: 115,687,580 (GRCm39)	K1146N	probably damaging	Het
Trdn	A	G	10: 33,109,883 (GRCm39)	T294A	possibly damaging	Het
Tsc22d1	T	C	14: 76,654,388 (GRCm39)	V289A	possibly damaging	Het
Tti1	C	A	2: 157,834,955 (GRCm39)	V1002L	possibly damaging	Het
Tubgcp4	T	A	2: 121,019,952 (GRCm39)		probably null	Het
Ush2a	G	A	1: 188,643,180 (GRCm39)	E4181K	possibly damaging	Het
Uvrag	A	G	7: 98,537,555 (GRCm39)	S547P	probably benign	Het
Vav3	T	C	3: 109,248,443 (GRCm39)	V30A	possibly damaging	Het
Vegfa	A	G	17: 46,336,395 (GRCm39)	Y242H	probably damaging	Het
Vmn2r75	G	T	7: 85,798,019 (GRCm39)	T598K	probably damaging	Het
Vps13b	C	T	15: 35,884,765 (GRCm39)	S3146L	possibly damaging	Het
Vrk3	A	G	7: 44,417,895 (GRCm39)	Y310C	probably damaging	Het
Zfhx4	A	G	3: 5,447,676 (GRCm39)	K1100R	probably benign	Het
Zfp748	T	A	13: 67,693,540 (GRCm39)		probably null	Het
Zfp760	A	T	17: 21,941,311 (GRCm39)	D162V	probably damaging	Het
Znfx1	T	A	2: 166,881,786 (GRCm39)	M1068L	probably damaging	Het

Other mutations in Exosc10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01400:Exosc10	APN	4	148,649,728 (GRCm39)	missense	probably damaging	1.00
IGL01591:Exosc10	APN	4	148,647,344 (GRCm39)	unclassified	probably benign
IGL01990:Exosc10	APN	4	148,650,867 (GRCm39)	missense	possibly damaging	0.83
IGL02137:Exosc10	APN	4	148,645,590 (GRCm39)	missense	probably damaging	0.97
IGL02186:Exosc10	APN	4	148,649,755 (GRCm39)	missense	probably damaging	0.96
IGL02412:Exosc10	APN	4	148,652,849 (GRCm39)	missense	probably benign	0.15
IGL02880:Exosc10	APN	4	148,660,640 (GRCm39)	missense	probably damaging	1.00
R0172:Exosc10	UTSW	4	148,649,814 (GRCm39)	missense	probably benign	0.02
R0267:Exosc10	UTSW	4	148,647,213 (GRCm39)	missense	probably damaging	1.00
R0592:Exosc10	UTSW	4	148,665,570 (GRCm39)	missense	probably benign
R1122:Exosc10	UTSW	4	148,650,821 (GRCm39)	missense	possibly damaging	0.86
R1218:Exosc10	UTSW	4	148,654,858 (GRCm39)	missense	probably damaging	1.00
R1498:Exosc10	UTSW	4	148,666,243 (GRCm39)	missense	possibly damaging	0.66
R1591:Exosc10	UTSW	4	148,652,840 (GRCm39)	missense	probably benign	0.04
R1719:Exosc10	UTSW	4	148,652,960 (GRCm39)	missense	probably damaging	1.00
R3727:Exosc10	UTSW	4	148,649,734 (GRCm39)	missense	probably damaging	1.00
R3842:Exosc10	UTSW	4	148,648,322 (GRCm39)	nonsense	probably null
R3876:Exosc10	UTSW	4	148,657,376 (GRCm39)	missense	probably benign	0.00
R4476:Exosc10	UTSW	4	148,649,781 (GRCm39)	missense	probably damaging	0.98
R4750:Exosc10	UTSW	4	148,646,851 (GRCm39)	missense	possibly damaging	0.69
R5306:Exosc10	UTSW	4	148,646,849 (GRCm39)	missense	probably benign	0.13
R5438:Exosc10	UTSW	4	148,650,799 (GRCm39)	nonsense	probably null
R5835:Exosc10	UTSW	4	148,649,844 (GRCm39)	missense	probably damaging	1.00
R5925:Exosc10	UTSW	4	148,657,819 (GRCm39)	missense	probably benign	0.01
R6116:Exosc10	UTSW	4	148,657,810 (GRCm39)	missense	probably benign	0.08
R6217:Exosc10	UTSW	4	148,666,768 (GRCm39)	splice site	probably null
R6365:Exosc10	UTSW	4	148,645,562 (GRCm39)	missense	probably benign	0.13
R6495:Exosc10	UTSW	4	148,647,329 (GRCm39)	missense	probably benign	0.45
R6498:Exosc10	UTSW	4	148,657,795 (GRCm39)	missense	probably benign
R6772:Exosc10	UTSW	4	148,665,591 (GRCm39)	missense	probably damaging	1.00
R7297:Exosc10	UTSW	4	148,664,834 (GRCm39)	missense	probably damaging	1.00
R7523:Exosc10	UTSW	4	148,648,299 (GRCm39)	critical splice acceptor site	probably null
R7698:Exosc10	UTSW	4	148,642,955 (GRCm39)	missense	probably benign
R7967:Exosc10	UTSW	4	148,649,121 (GRCm39)	missense	probably damaging	1.00
R8225:Exosc10	UTSW	4	148,649,661 (GRCm39)	missense	possibly damaging	0.86
R8477:Exosc10	UTSW	4	148,649,847 (GRCm39)	missense	possibly damaging	0.71
R8510:Exosc10	UTSW	4	148,648,646 (GRCm39)	missense	probably damaging	1.00
R8825:Exosc10	UTSW	4	148,653,159 (GRCm39)	critical splice donor site	probably null
R8826:Exosc10	UTSW	4	148,653,159 (GRCm39)	critical splice donor site	probably null
R9080:Exosc10	UTSW	4	148,649,121 (GRCm39)	missense	probably damaging	1.00
R9104:Exosc10	UTSW	4	148,664,859 (GRCm39)	missense	probably benign	0.03
R9159:Exosc10	UTSW	4	148,663,916 (GRCm39)	critical splice donor site	probably null
R9188:Exosc10	UTSW	4	148,643,017 (GRCm39)	missense	probably damaging	0.96
R9337:Exosc10	UTSW	4	148,665,588 (GRCm39)	missense	probably damaging	1.00
R9696:Exosc10	UTSW	4	148,649,704 (GRCm39)	missense	probably damaging	1.00
Z1177:Exosc10	UTSW	4	148,649,843 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCTCCATTGACTGGGAAGCAACTAC -3'
(R):5'- TCTTTCTCCACATGCAGAAGTGCTG -3'

Sequencing Primer
(F):5'- GGAAGCAACTACTTCCCAAGG -3'
(R):5'- CACATGCAGAAGTGCTGTGTTAC -3'

Posted On

2014-05-23