Mutagenetix > Incidental Mutations

Incidental Mutation 'R4870:Mipep'

376525

Institutional Source

Beutler Lab

Gene Symbol

Mipep

Ensembl Gene

ENSMUSG00000021993

Gene Name

mitochondrial intermediate peptidase

Synonyms

5730405E07Rik

MMRRC Submission

042480-MU

Accession Numbers

Is this an essential gene?

Probably essential (E-score: 0.960) question?

Stock #

R4870 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

60784573-60905478 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 60802880 bp

Zygosity

Heterozygous

Amino Acid Change

Leucine to Stop codon at position 283 (L283*)

Ref Sequence

ENSEMBL: ENSMUSP00000153374 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063562] [ENSMUST00000224635] [ENSMUST00000225043] [ENSMUST00000225506]

Predicted Effect

probably null
Transcript: ENSMUST00000063562
AA Change: L283*

SMART Domains

Protein: ENSMUSP00000069840
Gene: ENSMUSG00000021993
AA Change: L283*

Domain	Start	End	E-Value	Type
low complexity region	2	28	N/A	INTRINSIC
Pfam:Peptidase_M3	252	697	5.4e-145	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223709

Predicted Effect

probably null
Transcript: ENSMUST00000224635
AA Change: L283*

Predicted Effect

probably benign
Transcript: ENSMUST00000225043

Predicted Effect

probably null
Transcript: ENSMUST00000225506
AA Change: L283*

Meta Mutation Damage Score

0.9754

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 94.1%

Validation Efficiency

100% (77/77)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene performs the final step in processing a specific class of nuclear-encoded proteins targeted to the mitochondrial matrix or inner membrane. This protein is primarily involved in the maturation of oxidative phosphorylation (OXPHOS)-related proteins. This gene may contribute to the functional effects of frataxin deficiency and the clinical manifestations of Friedreich ataxia. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931406P16Rik	C	A	7: 34,284,887	V104L	possibly damaging	Het
Abcb11	A	T	2: 69,239,196	I1285N	probably damaging	Het
Abcc8	G	A	7: 46,107,259	R721*	probably null	Het
Alox8	T	C	11: 69,186,568	Y423C	probably damaging	Het
Ankle2	T	A	5: 110,251,478		probably null	Het
Cdc14a	A	G	3: 116,423,460	I9T	probably benign	Het
Ceacam18	T	C	7: 43,641,904	C257R	probably damaging	Het
Cilp	T	C	9: 65,279,698	V1025A	probably damaging	Het
Clcn7	G	T	17: 25,153,565		probably benign	Het
Csnk1d	A	T	11: 120,983,188		probably benign	Het
Cyp11b2	A	G	15: 74,853,146	S285P	probably benign	Het
Dip2b	T	A	15: 100,195,784		probably null	Het
Dmrt1	T	A	19: 25,505,855	M1K	probably null	Het
Dnajc14	T	C	10: 128,817,350	V684A	probably benign	Het
Dnmt3b	A	G	2: 153,670,364	Q335R	probably benign	Het
Exoc3l2	T	A	7: 19,495,192	C772S	unknown	Het
F2rl1	A	T	13: 95,513,984	F130Y	probably damaging	Het
Galk2	C	G	2: 125,929,637	S194*	probably null	Het
Gm7102	C	T	19: 61,175,926	G24R	unknown	Het
Gpbp1l1	A	G	4: 116,573,517	T62A	probably benign	Het
H2-Q10	A	T	17: 35,470,460	D53V	probably damaging	Het
H2-T22	T	C	17: 36,039,032	K356R	probably benign	Het
Insrr	G	A	3: 87,811,604	V956M	probably damaging	Het
Ints7	A	G	1: 191,596,331	T239A	probably damaging	Het
Isl1	A	G	13: 116,308,270		probably benign	Het
Kcng2	A	G	18: 80,322,868	C90R	probably benign	Het
Kif3c	C	T	12: 3,401,735	P171S	probably damaging	Het
Knl1	A	G	2: 119,081,513	T1704A	probably benign	Het
Lats1	A	G	10: 7,705,785	Y778C	probably damaging	Het
Limd2	T	C	11: 106,159,389	M1V	probably null	Het
Mcm10	A	T	2: 5,004,159	I333N	probably damaging	Het
Mixl1	A	G	1: 180,694,672	S215P	probably benign	Het
Mmp21	A	G	7: 133,678,677	L188P	probably damaging	Het
Mob1a	T	C	6: 83,340,239	S213P	probably benign	Het
Ndufaf6	T	C	4: 11,060,917	T220A	probably benign	Het
Nr4a3	A	T	4: 48,051,651	Y135F	possibly damaging	Het
Ntn1	CCTTCTTCT	CCTTCT	11: 68,213,026		probably benign	Het
Obscn	A	T	11: 59,136,206	L57Q	probably damaging	Het
Olfr1161	T	C	2: 88,025,460	L246P	probably damaging	Het
Olfr603	T	A	7: 103,383,633	D123V	probably damaging	Het
Pirb	T	A	7: 3,712,662	M839L	probably benign	Het
Plcl2	A	G	17: 50,607,226	E421G	possibly damaging	Het
Ppp1r12b	T	C	1: 134,949,033	N99S	probably benign	Het
Ptpro	A	G	6: 137,377,132	K169E	probably damaging	Het
Rita1	T	A	5: 120,611,383	K88N	probably damaging	Het
Rptn	A	T	3: 93,396,469	K370*	probably null	Het
Simc1	A	G	13: 54,539,763	D115G	probably null	Het
Stab1	T	A	14: 31,142,043	N136I	probably benign	Het
Syt4	T	A	18: 31,447,356		probably benign	Het
Sytl2	A	T	7: 90,388,898	N522I	probably damaging	Het
Tax1bp1	A	G	6: 52,729,493		probably benign	Het
Tenm2	A	T	11: 36,078,569	D847E	probably damaging	Het
Th	G	T	7: 142,894,097	D321E	probably benign	Het
Tmem44	A	T	16: 30,540,773	L46Q	probably damaging	Het
Trp53bp1	A	G	2: 121,256,641	L178P	probably damaging	Het
Trp63	A	G	16: 25,866,218	*285W	probably null	Het
Tsen34	T	C	7: 3,694,381		probably benign	Het
Tssk4	C	T	14: 55,651,815	T256I	probably benign	Het
Ttc17	A	T	2: 94,366,609	N464K	probably damaging	Het
Ttll2	C	T	17: 7,351,599	V310I	probably benign	Het
Ubn1	A	G	16: 5,077,313	E741G	probably damaging	Het
Urad	T	A	5: 147,315,454	I63F	probably damaging	Het
Vcan	T	C	13: 89,704,739	T701A	probably benign	Het
Vmn2r58	A	G	7: 41,837,215	V752A	possibly damaging	Het
Vmn2r69	C	A	7: 85,411,585	V264L	possibly damaging	Het
Zfp292	A	G	4: 34,808,917	S1376P	probably damaging	Het
Zfp955a	G	A	17: 33,241,725	R478*	probably null	Het
Znfx1	A	C	2: 167,055,269	F578L	probably benign	Het

Other mutations in Mipep

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00468:Mipep	APN	14	60875260	missense	probably benign	0.43
IGL00476:Mipep	APN	14	60827361	missense	probably damaging	1.00
IGL01319:Mipep	APN	14	60843271	missense	probably benign	0.00
IGL01608:Mipep	APN	14	60802230	missense	possibly damaging	0.65
IGL01621:Mipep	APN	14	60796165	splice site	probably benign
PIT4585001:Mipep	UTSW	14	60784835	missense	probably benign	0.01
R0635:Mipep	UTSW	14	60829390	missense	probably damaging	0.97
R1180:Mipep	UTSW	14	60834056	missense	probably damaging	1.00
R1463:Mipep	UTSW	14	60788146	splice site	probably benign
R1831:Mipep	UTSW	14	60872063	missense	probably damaging	1.00
R1833:Mipep	UTSW	14	60872063	missense	probably damaging	1.00
R1852:Mipep	UTSW	14	60843240	nonsense	probably null
R2115:Mipep	UTSW	14	60787380	missense	probably damaging	0.96
R2285:Mipep	UTSW	14	60787394	missense	possibly damaging	0.94
R3890:Mipep	UTSW	14	60808995	missense	probably damaging	1.00
R3892:Mipep	UTSW	14	60808995	missense	probably damaging	1.00
R4078:Mipep	UTSW	14	60846477	missense	probably damaging	1.00
R4509:Mipep	UTSW	14	60827321	missense	probably damaging	1.00
R4619:Mipep	UTSW	14	60903416	missense	probably damaging	0.97
R4707:Mipep	UTSW	14	60872103	missense	probably damaging	0.98
R4804:Mipep	UTSW	14	60802952	missense	probably damaging	1.00
R4964:Mipep	UTSW	14	60784782	missense	probably damaging	0.97
R4966:Mipep	UTSW	14	60784782	missense	probably damaging	0.97
R4984:Mipep	UTSW	14	60788182	missense	possibly damaging	0.87
R5074:Mipep	UTSW	14	60809013	missense	probably benign	0.02
R5090:Mipep	UTSW	14	60802299	missense	possibly damaging	0.92
R5131:Mipep	UTSW	14	60903374	missense	probably damaging	1.00
R5569:Mipep	UTSW	14	60802934	missense	probably damaging	1.00
R6162:Mipep	UTSW	14	60787404	missense	probably damaging	0.99
R6195:Mipep	UTSW	14	60872105	missense	probably damaging	1.00
R6233:Mipep	UTSW	14	60872105	missense	probably damaging	1.00
R6680:Mipep	UTSW	14	60788223	missense	possibly damaging	0.67
R7120:Mipep	UTSW	14	60875247	missense	possibly damaging	0.60
R7470:Mipep	UTSW	14	60802895	missense	probably benign	0.31
R7826:Mipep	UTSW	14	60802131	missense	probably damaging	1.00
R7869:Mipep	UTSW	14	60802936	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGACCTGATGTGGCCTGTTG -3'
(R):5'- GCTCTCCAGTGCTGTCAATC -3'

Sequencing Primer
(F):5'- TTTGGAAGCCATGGCCAG -3'
(R):5'- CTCTTGACCCTCCCACTAGAACG -3'

Posted On

2016-03-17