Incidental Mutation 'R4789:Mios'
ID 367310
Institutional Source Beutler Lab
Gene Symbol Mios
Ensembl Gene ENSMUSG00000042447
Gene Name meiosis regulator for oocyte development
Synonyms
Accession Numbers
Essential gene? Probably essential (E-score: 0.946) question?
Stock # R4789 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 8209222-8236274 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 8235429 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Threonine at position 859 (M859T)
Ref Sequence ENSEMBL: ENSMUSP00000039301 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040017]
AlphaFold Q8VE19
Predicted Effect probably benign
Transcript: ENSMUST00000040017
AA Change: M859T

PolyPhen 2 Score 0.061 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000039301
Gene: ENSMUSG00000042447
AA Change: M859T

DomainStartEndE-ValueType
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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160265
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161134
Coding Region Coverage
  • 1x: 98.8%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 94.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110004F10Rik C A 7: 115,692,757 (GRCm39) D20E probably benign Het
Abcb9 T A 5: 124,216,853 (GRCm39) M455L probably benign Het
Add2 G A 6: 86,095,752 (GRCm39) V475M probably benign Het
Apoh T A 11: 108,300,064 (GRCm39) Y238N probably damaging Het
Arpp21 A G 9: 111,896,360 (GRCm39) S681P probably benign Het
Atp1a3 A C 7: 24,698,389 (GRCm39) F149C probably damaging Het
B9d1 A G 11: 61,397,186 (GRCm39) D27G probably benign Het
Bfar T A 16: 13,503,001 (GRCm39) M1K probably null Het
Bok T C 1: 93,616,963 (GRCm39) V103A probably damaging Het
Brca1 A C 11: 101,414,758 (GRCm39) H1125Q probably benign Het
Card9 T A 2: 26,247,632 (GRCm39) M218L probably damaging Het
Cers1 T C 8: 70,776,018 (GRCm39) V303A probably damaging Het
Col6a5 T C 9: 105,814,534 (GRCm39) I493V unknown Het
Coro7 T C 16: 4,446,085 (GRCm39) Y880C probably damaging Het
Cyp2b19 T C 7: 26,463,801 (GRCm39) Y318H probably benign Het
Dennd3 T A 15: 73,394,131 (GRCm39) L52Q probably damaging Het
Dlat A T 9: 50,570,670 (GRCm39) C33S probably benign Het
Dmxl2 T A 9: 54,287,099 (GRCm39) Q2646L probably benign Het
Dnah3 T C 7: 119,610,295 (GRCm39) N1703D probably damaging Het
Dock10 T A 1: 80,518,998 (GRCm39) H1241L probably damaging Het
Fbxl17 T G 17: 63,794,910 (GRCm39) I391L probably benign Het
Fdxacb1 A G 9: 50,681,418 (GRCm39) D113G possibly damaging Het
Flii A G 11: 60,605,919 (GRCm39) S1185P probably benign Het
Gm14496 A T 2: 181,637,577 (GRCm39) Q217L possibly damaging Het
Heatr9 A T 11: 83,410,018 (GRCm39) D74E probably benign Het
Heca C A 10: 17,783,895 (GRCm39) E91* probably null Het
Ikzf4 T G 10: 128,468,575 (GRCm39) T635P probably benign Het
Kif17 C T 4: 138,008,688 (GRCm39) P382S probably damaging Het
Kmt5b T C 19: 3,865,330 (GRCm39) V775A probably benign Het
Mapk8ip2 T A 15: 89,343,241 (GRCm39) F661Y probably damaging Het
Mapkap1 A G 2: 34,423,859 (GRCm39) E111G possibly damaging Het
Med9 T A 11: 59,839,266 (GRCm39) N58K probably benign Het
Mid2 T A X: 139,578,981 (GRCm39) Y61N probably damaging Het
Mief1 T A 15: 80,132,080 (GRCm39) Y50* probably null Het
Muc5ac G T 7: 141,352,619 (GRCm39) C702F possibly damaging Het
Nkiras1 T C 14: 18,276,935 (GRCm38) probably benign Het
Or11i1 A C 3: 106,729,608 (GRCm39) I89R possibly damaging Het
Or11i1 T A 3: 106,729,624 (GRCm39) M84L possibly damaging Het
Or56a3b T G 7: 104,771,520 (GRCm39) H285Q probably null Het
Or5ae2 T A 7: 84,506,509 (GRCm39) C311S probably benign Het
Pcsk5 C T 19: 17,410,963 (GRCm39) V1810M probably benign Het
Pex1 T C 5: 3,680,270 (GRCm39) V964A probably damaging Het
Pgm2l1 A T 7: 99,916,794 (GRCm39) M471L probably benign Het
Pkd1l2 T C 8: 117,738,314 (GRCm39) T2182A probably damaging Het
Plscr1l1 G A 9: 92,233,084 (GRCm39) C69Y probably damaging Het
Polr1b T A 2: 128,951,257 (GRCm39) I290K probably benign Het
Prkg1 T A 19: 31,563,045 (GRCm39) M119L probably damaging Het
Rbl1 A G 2: 157,019,275 (GRCm39) V490A probably benign Het
Shtn1 G C 19: 59,039,305 (GRCm39) R45G probably damaging Het
Slc10a6 T A 5: 103,776,848 (GRCm39) Y84F probably benign Het
Slc25a23 T C 17: 57,366,597 (GRCm39) D26G probably damaging Het
Slc41a2 T C 10: 83,152,320 (GRCm39) K52E probably damaging Het
Slc4a5 T C 6: 83,247,951 (GRCm39) F501L probably benign Het
Slfn5 T A 11: 82,847,226 (GRCm39) M37K probably benign Het
Sptbn1 A C 11: 30,067,759 (GRCm39) F1818L probably benign Het
Taf3 T C 2: 9,956,770 (GRCm39) T466A probably damaging Het
Thbs2 C T 17: 14,891,750 (GRCm39) G929D probably damaging Het
Tmc3 A T 7: 83,271,746 (GRCm39) D995V probably damaging Het
Tmem262 T C 19: 6,130,452 (GRCm39) F59L possibly damaging Het
Triobp A G 15: 78,875,228 (GRCm39) D137G probably damaging Het
Tspear T C 10: 77,702,199 (GRCm39) F211L possibly damaging Het
Ttn A T 2: 76,728,670 (GRCm39) probably benign Het
Ugt2b5 T A 5: 87,287,550 (GRCm39) M206L probably benign Het
Ush1g A T 11: 115,209,466 (GRCm39) S243T probably damaging Het
Usp19 A T 9: 108,370,433 (GRCm39) T86S possibly damaging Het
Wdhd1 A G 14: 47,506,149 (GRCm39) V255A probably benign Het
Wdr11 G A 7: 129,220,394 (GRCm39) W594* probably null Het
Wnk3 T A X: 149,993,933 (GRCm39) Y331* probably null Het
Zfp429 A T 13: 67,538,523 (GRCm39) I307K probably benign Het
Zkscan14 T A 5: 145,132,444 (GRCm39) K362N probably damaging Het
Other mutations in Mios
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01089:Mios APN 6 8,234,363 (GRCm39) critical splice donor site probably null
IGL01365:Mios APN 6 8,216,089 (GRCm39) nonsense probably null
IGL01548:Mios APN 6 8,234,252 (GRCm39) missense possibly damaging 0.90
IGL01898:Mios APN 6 8,222,668 (GRCm39) missense probably benign 0.03
IGL02110:Mios APN 6 8,215,565 (GRCm39) missense probably damaging 1.00
IGL02308:Mios APN 6 8,231,269 (GRCm39) missense probably benign 0.06
IGL02375:Mios APN 6 8,222,598 (GRCm39) missense probably benign 0.02
IGL02452:Mios APN 6 8,222,492 (GRCm39) missense probably benign 0.01
IGL02670:Mios APN 6 8,235,378 (GRCm39) splice site probably benign
IGL03083:Mios APN 6 8,215,156 (GRCm39) missense probably damaging 1.00
R0462:Mios UTSW 6 8,215,743 (GRCm39) missense probably benign 0.11
R0591:Mios UTSW 6 8,215,470 (GRCm39) missense possibly damaging 0.52
R1351:Mios UTSW 6 8,228,120 (GRCm39) missense possibly damaging 0.70
R1476:Mios UTSW 6 8,234,237 (GRCm39) missense probably benign 0.01
R1802:Mios UTSW 6 8,216,385 (GRCm39) nonsense probably null
R1959:Mios UTSW 6 8,215,437 (GRCm39) missense probably benign 0.17
R1964:Mios UTSW 6 8,215,798 (GRCm39) missense probably damaging 0.99
R2272:Mios UTSW 6 8,226,865 (GRCm39) missense possibly damaging 0.71
R2915:Mios UTSW 6 8,214,935 (GRCm39) missense possibly damaging 0.72
R3852:Mios UTSW 6 8,216,453 (GRCm39) missense probably benign 0.09
R3876:Mios UTSW 6 8,233,189 (GRCm39) missense probably damaging 0.98
R3948:Mios UTSW 6 8,215,496 (GRCm39) missense probably benign
R4698:Mios UTSW 6 8,228,113 (GRCm39) missense possibly damaging 0.60
R4785:Mios UTSW 6 8,222,464 (GRCm39) missense probably benign
R4866:Mios UTSW 6 8,214,857 (GRCm39) missense probably damaging 1.00
R4878:Mios UTSW 6 8,215,094 (GRCm39) missense probably benign 0.00
R4991:Mios UTSW 6 8,215,847 (GRCm39) missense probably benign 0.00
R5479:Mios UTSW 6 8,215,314 (GRCm39) missense probably benign 0.00
R5714:Mios UTSW 6 8,215,434 (GRCm39) missense probably damaging 0.99
R6030:Mios UTSW 6 8,215,704 (GRCm39) missense probably benign 0.11
R6030:Mios UTSW 6 8,215,704 (GRCm39) missense probably benign 0.11
R6111:Mios UTSW 6 8,214,836 (GRCm39) missense probably benign 0.01
R6455:Mios UTSW 6 8,231,239 (GRCm39) missense probably benign 0.03
R7381:Mios UTSW 6 8,216,064 (GRCm39) missense probably damaging 0.98
R8350:Mios UTSW 6 8,227,998 (GRCm39) missense probably benign 0.00
R8708:Mios UTSW 6 8,234,255 (GRCm39) missense probably benign 0.17
R8913:Mios UTSW 6 8,215,924 (GRCm39) missense probably benign
R9062:Mios UTSW 6 8,233,221 (GRCm39) missense probably benign 0.00
R9359:Mios UTSW 6 8,214,894 (GRCm39) missense probably benign 0.17
R9521:Mios UTSW 6 8,233,171 (GRCm39) missense probably benign 0.45
Predicted Primers PCR Primer
(F):5'- GACTGTGAGCAAGCCATTTTGG -3'
(R):5'- ACATTGCTGAGCTGACAGAATG -3'

Sequencing Primer
(F):5'- CTCTTAAAAGTTCACCTTGGTGATTG -3'
(R):5'- GCTTTATTTTTCCACGACAGCAAAGC -3'
Posted On 2015-12-29