Mutagenetix > Incidental Mutation

Incidental Mutation 'R4878:Mios'

375058

Institutional Source

Beutler Lab

Gene Symbol

Mios

Ensembl Gene

ENSMUSG00000042447

Gene Name

meiosis regulator for oocyte development

Synonyms

MMRRC Submission

042487-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.951) question?

Stock #

R4878 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

8209222-8236274 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 8215094 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Aspartic acid at position 97 (N97D)

Ref Sequence

ENSEMBL: ENSMUSP00000039301 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040017]

AlphaFold

Q8VE19

Predicted Effect

probably benign
Transcript: ENSMUST00000040017
AA Change: N97D

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000039301
Gene: ENSMUSG00000042447
AA Change: N97D

Domain	Start	End	E-Value	Type
Blast:WD40	49	91	2e-18	BLAST
WD40	101	146	2.05e1	SMART
WD40	174	212	3.55e1	SMART
WD40	214	252	2.45e2	SMART
WD40	256	297	6.42e-1	SMART
Blast:WD40	312	354	2e-13	BLAST
Pfam:zinc_ribbon_16	737	861	1.3e-26	PFAM

Meta Mutation Damage Score

0.0681

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.8%
20x: 93.8%

Validation Efficiency

96% (70/73)

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4	C	A	4: 144,613,845	H47N	possibly damaging	Het
Adgrg3	A	T	8: 95,035,086	N159I	possibly damaging	Het
Agrn	A	T	4: 156,170,845	L1449Q	probably damaging	Het
Anks6	C	T	4: 47,030,795	G601S	probably damaging	Het
Atg2a	A	T	19: 6,250,244	E694V	probably damaging	Het
Ccndbp1	T	A	2: 121,014,691	L363*	probably null	Het
Cdh16	A	T	8: 104,618,064	D478E	probably damaging	Het
Cep295	A	T	9: 15,334,956	W735R	probably benign	Het
Cnnm2	C	T	19: 46,859,083	P682S	probably benign	Het
Daam2	C	A	17: 49,460,710	R951L	probably damaging	Het
Dmxl1	T	A	18: 49,851,476	F180I	probably damaging	Het
Dnajc6	T	C	4: 101,599,034		probably benign	Het
Efemp2	A	T	19: 5,480,761		probably benign	Het
Emilin1	A	G	5: 30,917,066	D217G	probably benign	Het
Enpep	A	T	3: 129,276,771	M829K	probably benign	Het
Epb41l4a	A	G	18: 33,798,572	V623A	probably damaging	Het
Erlin2	T	A	8: 27,027,166		probably null	Het
Fbln2	T	C	6: 91,256,995		probably null	Het
Gga3	A	T	11: 115,591,321	I157N	probably damaging	Het
Gm884	A	G	11: 103,617,891		probably benign	Het
Gtpbp6	C	T	5: 110,107,311		probably benign	Het
Hps4	T	C	5: 112,375,368	V584A	probably benign	Het
Ighv1-50	T	C	12: 115,119,947	Y51C	probably benign	Het
Kif13b	T	C	14: 64,806,154	L1801P	probably benign	Het
Kif16b	T	C	2: 142,848,003	I330V	probably damaging	Het
Klb	A	T	5: 65,348,490	R27W	probably damaging	Het
Lrif1	A	T	3: 106,735,640	K169M	probably damaging	Het
Met	A	G	6: 17,549,059	D970G	probably damaging	Het
Mical3	A	T	6: 120,969,387	M1051K	possibly damaging	Het
Msh5	G	A	17: 35,038,456	R321C	probably damaging	Het
Mybpc1	T	C	10: 88,551,430	Q473R	possibly damaging	Het
Ncoa1	C	T	12: 4,275,004	G970D	probably damaging	Het
Neb	T	C	2: 52,219,394	Y232C	probably damaging	Het
Nefh	A	G	11: 4,941,333	S429P	probably damaging	Het
Notch3	C	T	17: 32,147,085	G1014D	probably damaging	Het
Nup107	A	T	10: 117,751,418	C859S	probably benign	Het
Olfr1033	A	G	2: 86,041,455	I47V	probably benign	Het
Olfr136	T	G	17: 38,335,627	F157V	probably benign	Het
Olfr412	T	C	11: 74,364,848	Y60H	probably damaging	Het
Otud7b	T	A	3: 96,136,510		probably benign	Het
Pde1a	A	T	2: 79,878,139	S312T	probably benign	Het
Piwil1	G	T	5: 128,740,981	R94L	probably damaging	Het
Pnma2	G	A	14: 66,917,054	W309*	probably null	Het
Ppef2	A	C	5: 92,228,740		probably null	Het
Rabac1	T	A	7: 24,969,967	Q212L	possibly damaging	Het
Rad51	T	C	2: 119,120,492		probably benign	Het
Rbm48	A	T	5: 3,591,853		probably benign	Het
Rft1	C	T	14: 30,677,804	S315L	probably benign	Het
Rgs13	C	T	1: 144,171,479	M1I	probably null	Het
Rhbg	A	C	3: 88,247,453	S215A	probably benign	Het
Rufy2	A	T	10: 63,002,211	N379I	probably damaging	Het
Slc17a1	T	C	13: 23,880,654	L367P	probably damaging	Het
Slc25a39	G	A	11: 102,403,675	R308C	probably benign	Het
Smo	A	G	6: 29,753,571	T149A	probably benign	Het
Sqle	A	G	15: 59,316,085	K81E	probably benign	Het
Tfpi	A	G	2: 84,452,555		probably null	Het
Tnk2	A	G	16: 32,679,630	D572G	probably damaging	Het
Ubr5	A	T	15: 38,006,564	M1149K	probably benign	Het
Utrn	T	A	10: 12,727,758	Q626L	probably damaging	Het
Virma	T	A	4: 11,544,971	H1643Q	probably damaging	Het
Wnt3	G	T	11: 103,808,205	G46C	possibly damaging	Het
Zkscan7	G	T	9: 122,890,800	G184*	probably null	Het

Other mutations in Mios

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01089:Mios	APN	6	8,234,363 (GRCm38)	critical splice donor site	probably null
IGL01365:Mios	APN	6	8,216,089 (GRCm38)	nonsense	probably null
IGL01548:Mios	APN	6	8,234,252 (GRCm38)	missense	possibly damaging	0.90
IGL01898:Mios	APN	6	8,222,668 (GRCm38)	missense	probably benign	0.03
IGL02110:Mios	APN	6	8,215,565 (GRCm38)	missense	probably damaging	1.00
IGL02308:Mios	APN	6	8,231,269 (GRCm38)	missense	probably benign	0.06
IGL02375:Mios	APN	6	8,222,598 (GRCm38)	missense	probably benign	0.02
IGL02452:Mios	APN	6	8,222,492 (GRCm38)	missense	probably benign	0.01
IGL02670:Mios	APN	6	8,235,378 (GRCm38)	splice site	probably benign
IGL03083:Mios	APN	6	8,215,156 (GRCm38)	missense	probably damaging	1.00
R0462:Mios	UTSW	6	8,215,743 (GRCm38)	missense	probably benign	0.11
R0591:Mios	UTSW	6	8,215,470 (GRCm38)	missense	possibly damaging	0.52
R1351:Mios	UTSW	6	8,228,120 (GRCm38)	missense	possibly damaging	0.70
R1476:Mios	UTSW	6	8,234,237 (GRCm38)	missense	probably benign	0.01
R1802:Mios	UTSW	6	8,216,385 (GRCm38)	nonsense	probably null
R1959:Mios	UTSW	6	8,215,437 (GRCm38)	missense	probably benign	0.17
R1964:Mios	UTSW	6	8,215,798 (GRCm38)	missense	probably damaging	0.99
R2272:Mios	UTSW	6	8,226,865 (GRCm38)	missense	possibly damaging	0.71
R2915:Mios	UTSW	6	8,214,935 (GRCm38)	missense	possibly damaging	0.72
R3852:Mios	UTSW	6	8,216,453 (GRCm38)	missense	probably benign	0.09
R3876:Mios	UTSW	6	8,233,189 (GRCm38)	missense	probably damaging	0.98
R3948:Mios	UTSW	6	8,215,496 (GRCm38)	missense	probably benign
R4698:Mios	UTSW	6	8,228,113 (GRCm38)	missense	possibly damaging	0.60
R4785:Mios	UTSW	6	8,222,464 (GRCm38)	missense	probably benign
R4789:Mios	UTSW	6	8,235,429 (GRCm38)	missense	probably benign	0.06
R4866:Mios	UTSW	6	8,214,857 (GRCm38)	missense	probably damaging	1.00
R4991:Mios	UTSW	6	8,215,847 (GRCm38)	missense	probably benign	0.00
R5479:Mios	UTSW	6	8,215,314 (GRCm38)	missense	probably benign	0.00
R5714:Mios	UTSW	6	8,215,434 (GRCm38)	missense	probably damaging	0.99
R6030:Mios	UTSW	6	8,215,704 (GRCm38)	missense	probably benign	0.11
R6030:Mios	UTSW	6	8,215,704 (GRCm38)	missense	probably benign	0.11
R6111:Mios	UTSW	6	8,214,836 (GRCm38)	missense	probably benign	0.01
R6455:Mios	UTSW	6	8,231,239 (GRCm38)	missense	probably benign	0.03
R7381:Mios	UTSW	6	8,216,064 (GRCm38)	missense	probably damaging	0.98
R8350:Mios	UTSW	6	8,227,998 (GRCm38)	missense	probably benign	0.00
R8708:Mios	UTSW	6	8,234,255 (GRCm38)	missense	probably benign	0.17
R8913:Mios	UTSW	6	8,215,924 (GRCm38)	missense	probably benign
R9062:Mios	UTSW	6	8,233,221 (GRCm38)	missense	probably benign	0.00
R9359:Mios	UTSW	6	8,214,894 (GRCm38)	missense	probably benign	0.17
R9521:Mios	UTSW	6	8,233,171 (GRCm38)	missense	probably benign	0.45

Predicted Primers

PCR Primer
(F):5'- TGAATTCAGAACTCAAAGCTGGATC -3'
(R):5'- GCTTCACCTGCTGAAAGTCTC -3'

Sequencing Primer
(F):5'- ACTCAAAGCTGGATCGTTACG -3'
(R):5'- AAGTCTCACTTTTTCCATGGGAAC -3'

Posted On

2016-03-17