Incidental Mutation 'R6182:Mroh9'
ID 487006
Institutional Source Beutler Lab
Gene Symbol Mroh9
Ensembl Gene ENSMUSG00000071890
Gene Name maestro heat-like repeat family member 9
Synonyms 4921528O07Rik, Armc11
MMRRC Submission 044324-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6182 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 162851871-162913239 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 162893612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 188 (Q188*)
Ref Sequence ENSEMBL: ENSMUSP00000094365 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096608]
AlphaFold G5E8L9
Predicted Effect probably null
Transcript: ENSMUST00000096608
AA Change: Q188*
SMART Domains Protein: ENSMUSP00000094365
Gene: ENSMUSG00000071890
AA Change: Q188*

DomainStartEndE-ValueType
SCOP:d1gw5b_ 231 716 2e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195132
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.3%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts7 T C 9: 90,074,489 (GRCm39) S884P probably benign Het
Akap13 C A 7: 75,236,028 (GRCm39) A201E probably benign Het
Ces1f T G 8: 93,983,124 (GRCm39) E540A probably benign Het
Chid1 T A 7: 141,108,415 (GRCm39) M137L probably benign Het
Chsy3 A G 18: 59,312,414 (GRCm39) T296A probably benign Het
Clec4f A G 6: 83,622,284 (GRCm39) V519A probably benign Het
Clk4 T A 11: 51,159,009 (GRCm39) F41I possibly damaging Het
Cntnap5c A G 17: 58,183,390 (GRCm39) D32G probably benign Het
Ctsl T C 13: 64,515,786 (GRCm39) Y95C probably damaging Het
Cyp2c54 T C 19: 40,036,005 (GRCm39) M302V probably benign Het
Cyp2c65 C G 19: 39,049,606 (GRCm39) L45V probably benign Het
Cyp2j6 G C 4: 96,424,323 (GRCm39) L145V probably damaging Het
Daam1 C T 12: 72,006,661 (GRCm39) Q693* probably null Het
Dgcr8 A T 16: 18,098,172 (GRCm39) D406E probably benign Het
Dock2 G T 11: 34,179,476 (GRCm39) P1760Q probably damaging Het
Epb41l2 G A 10: 25,383,715 (GRCm39) R940H probably damaging Het
Erc2 A C 14: 28,039,210 (GRCm39) D951A probably damaging Het
Fbxw7 T C 3: 84,723,078 (GRCm39) probably null Het
Frem2 T A 3: 53,555,390 (GRCm39) I1716F probably damaging Het
Fus A G 7: 127,576,465 (GRCm39) D295G probably damaging Het
Gm5093 A G 17: 46,750,568 (GRCm39) I153T probably benign Het
Gnptab T C 10: 88,265,342 (GRCm39) V318A possibly damaging Het
Gpc2 T C 5: 138,276,676 (GRCm39) D150G probably benign Het
Gsc2 A G 16: 17,731,483 (GRCm39) *215R probably null Het
Hectd3 T C 4: 116,857,476 (GRCm39) S552P probably damaging Het
Katnal1 C A 5: 148,841,407 (GRCm39) K152N possibly damaging Het
Kcnh1 A T 1: 191,873,361 (GRCm39) T16S probably damaging Het
Lrrc71 T C 3: 87,653,101 (GRCm39) D105G probably benign Het
Mon2 T C 10: 122,874,564 (GRCm39) probably null Het
Mtmr14 A G 6: 113,246,469 (GRCm39) S81G possibly damaging Het
Nrap T A 19: 56,350,130 (GRCm39) M628L probably benign Het
Odad3 A G 9: 21,901,698 (GRCm39) F553S probably damaging Het
Or1o1 T A 17: 37,716,883 (GRCm39) I148K possibly damaging Het
Or5k1 A G 16: 58,617,655 (GRCm39) Y185H probably damaging Het
Pals2 A G 6: 50,175,206 (GRCm39) I506V probably benign Het
Pate4 A T 9: 35,519,586 (GRCm39) S35T possibly damaging Het
Pkd1l1 T C 11: 8,815,555 (GRCm39) E1452G probably benign Het
Pld5 T C 1: 175,872,420 (GRCm39) D239G probably benign Het
Ppef2 C T 5: 92,374,925 (GRCm39) V728M probably damaging Het
Rasip1 TGCCGCCGCCGCCGCCGCCGCCGC TGCCGCCGCCGCCGCCGCCGC 7: 45,277,879 (GRCm39) probably benign Het
Rsf1 G A 7: 97,229,117 (GRCm39) probably benign Het
Serpina3c C A 12: 104,115,690 (GRCm39) V285L probably benign Het
Serpinb9f T C 13: 33,518,405 (GRCm39) S302P probably damaging Het
Sis C T 3: 72,811,626 (GRCm39) V1642I probably benign Het
Slc12a4 G A 8: 106,674,531 (GRCm39) L601F probably damaging Het
Slc39a6 G T 18: 24,734,013 (GRCm39) N225K probably benign Het
Snrnp70 G A 7: 45,026,497 (GRCm39) R291* probably null Het
Spin1 C T 13: 51,298,374 (GRCm39) T131I probably benign Het
St18 T G 1: 6,914,342 (GRCm39) probably null Het
Stox1 A G 10: 62,500,721 (GRCm39) L613P probably damaging Het
Tgm3 T G 2: 129,867,221 (GRCm39) Y155* probably null Het
Tmem67 T C 4: 12,051,402 (GRCm39) I809V probably benign Het
Tnc T A 4: 63,927,033 (GRCm39) D831V probably damaging Het
Ttll13 A T 7: 79,909,981 (GRCm39) E762D probably benign Het
Unc5b A T 10: 60,601,015 (GRCm39) V937E probably damaging Het
Vmn1r34 A G 6: 66,614,312 (GRCm39) I142T probably damaging Het
Vmn2r104 A G 17: 20,250,507 (GRCm39) M588T probably benign Het
Vmn2r77 T C 7: 86,460,957 (GRCm39) V761A probably damaging Het
Wdr48 G T 9: 119,753,832 (GRCm39) G665W probably damaging Het
Xpot T A 10: 121,442,163 (GRCm39) R550S probably damaging Het
Ydjc A G 16: 16,964,943 (GRCm39) T33A probably benign Het
Zfc3h1 A G 10: 115,226,764 (GRCm39) T274A probably benign Het
Zfp202 G A 9: 40,118,638 (GRCm39) G17E probably damaging Het
Zfp788 T A 7: 41,299,940 (GRCm39) C859S probably damaging Het
Zscan4c T C 7: 10,740,709 (GRCm39) M76T probably benign Het
Other mutations in Mroh9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00593:Mroh9 APN 1 162,873,350 (GRCm39) missense possibly damaging 0.89
IGL00705:Mroh9 APN 1 162,907,072 (GRCm39) missense probably damaging 1.00
IGL00788:Mroh9 APN 1 162,852,227 (GRCm39) missense probably benign 0.06
IGL00795:Mroh9 APN 1 162,888,191 (GRCm39) missense probably damaging 1.00
IGL00815:Mroh9 APN 1 162,866,700 (GRCm39) missense probably damaging 1.00
IGL01025:Mroh9 APN 1 162,875,435 (GRCm39) missense possibly damaging 0.67
IGL01303:Mroh9 APN 1 162,908,144 (GRCm39) missense probably benign 0.00
IGL01526:Mroh9 APN 1 162,883,172 (GRCm39) missense probably damaging 0.99
IGL01680:Mroh9 APN 1 162,875,551 (GRCm39) splice site probably null
IGL01823:Mroh9 APN 1 162,883,178 (GRCm39) missense probably benign 0.39
IGL02024:Mroh9 APN 1 162,890,071 (GRCm39) missense possibly damaging 0.65
IGL02213:Mroh9 APN 1 162,885,648 (GRCm39) missense probably damaging 1.00
IGL02455:Mroh9 APN 1 162,903,149 (GRCm39) missense probably benign 0.03
IGL02546:Mroh9 APN 1 162,908,145 (GRCm39) missense probably benign 0.04
IGL03059:Mroh9 APN 1 162,852,205 (GRCm39) missense possibly damaging 0.95
IGL03061:Mroh9 APN 1 162,854,071 (GRCm39) missense probably damaging 1.00
IGL03071:Mroh9 APN 1 162,866,766 (GRCm39) missense probably damaging 1.00
R0048:Mroh9 UTSW 1 162,890,056 (GRCm39) missense probably damaging 0.97
R0048:Mroh9 UTSW 1 162,890,056 (GRCm39) missense probably damaging 0.97
R0441:Mroh9 UTSW 1 162,888,331 (GRCm39) missense probably damaging 1.00
R0506:Mroh9 UTSW 1 162,888,205 (GRCm39) missense possibly damaging 0.90
R0629:Mroh9 UTSW 1 162,888,205 (GRCm39) missense possibly damaging 0.90
R0751:Mroh9 UTSW 1 162,893,693 (GRCm39) missense possibly damaging 0.84
R1301:Mroh9 UTSW 1 162,871,552 (GRCm39) critical splice donor site probably null
R1481:Mroh9 UTSW 1 162,854,078 (GRCm39) missense probably damaging 1.00
R1618:Mroh9 UTSW 1 162,852,110 (GRCm39) missense probably benign 0.00
R1647:Mroh9 UTSW 1 162,873,625 (GRCm39) missense probably damaging 1.00
R1648:Mroh9 UTSW 1 162,873,625 (GRCm39) missense probably damaging 1.00
R1668:Mroh9 UTSW 1 162,852,161 (GRCm39) missense possibly damaging 0.52
R1795:Mroh9 UTSW 1 162,884,347 (GRCm39) missense probably damaging 0.97
R1796:Mroh9 UTSW 1 162,873,279 (GRCm39) missense probably damaging 1.00
R1857:Mroh9 UTSW 1 162,866,714 (GRCm39) missense probably damaging 0.98
R1869:Mroh9 UTSW 1 162,854,082 (GRCm39) missense probably damaging 0.97
R1923:Mroh9 UTSW 1 162,903,860 (GRCm39) missense probably damaging 1.00
R2325:Mroh9 UTSW 1 162,854,099 (GRCm39) splice site probably null
R2511:Mroh9 UTSW 1 162,866,514 (GRCm39) missense probably benign 0.13
R2912:Mroh9 UTSW 1 162,871,572 (GRCm39) missense probably damaging 1.00
R2913:Mroh9 UTSW 1 162,871,572 (GRCm39) missense probably damaging 1.00
R2919:Mroh9 UTSW 1 162,884,341 (GRCm39) missense probably damaging 1.00
R2973:Mroh9 UTSW 1 162,884,338 (GRCm39) missense probably damaging 1.00
R3912:Mroh9 UTSW 1 162,893,638 (GRCm39) missense probably damaging 0.97
R4034:Mroh9 UTSW 1 162,908,122 (GRCm39) critical splice donor site probably null
R4551:Mroh9 UTSW 1 162,871,662 (GRCm39) missense probably damaging 0.98
R4656:Mroh9 UTSW 1 162,893,593 (GRCm39) missense probably damaging 1.00
R4662:Mroh9 UTSW 1 162,883,162 (GRCm39) missense probably damaging 0.97
R4743:Mroh9 UTSW 1 162,852,061 (GRCm39) missense probably benign 0.05
R4890:Mroh9 UTSW 1 162,854,093 (GRCm39) missense probably damaging 1.00
R5128:Mroh9 UTSW 1 162,888,329 (GRCm39) missense probably damaging 1.00
R5129:Mroh9 UTSW 1 162,888,329 (GRCm39) missense probably damaging 1.00
R5147:Mroh9 UTSW 1 162,888,329 (GRCm39) missense probably damaging 1.00
R5157:Mroh9 UTSW 1 162,871,690 (GRCm39) missense probably damaging 0.96
R5324:Mroh9 UTSW 1 162,888,329 (GRCm39) missense probably damaging 1.00
R5325:Mroh9 UTSW 1 162,888,329 (GRCm39) missense probably damaging 1.00
R5340:Mroh9 UTSW 1 162,908,156 (GRCm39) start gained probably benign
R6005:Mroh9 UTSW 1 162,903,246 (GRCm39) missense probably damaging 0.99
R6414:Mroh9 UTSW 1 162,902,271 (GRCm39) missense probably damaging 1.00
R6477:Mroh9 UTSW 1 162,903,873 (GRCm39) missense probably damaging 1.00
R6540:Mroh9 UTSW 1 162,866,541 (GRCm39) missense possibly damaging 0.87
R6541:Mroh9 UTSW 1 162,885,607 (GRCm39) missense possibly damaging 0.78
R6643:Mroh9 UTSW 1 162,903,130 (GRCm39) missense probably damaging 1.00
R6811:Mroh9 UTSW 1 162,873,610 (GRCm39) missense possibly damaging 0.86
R6830:Mroh9 UTSW 1 162,903,935 (GRCm39) missense probably benign
R7026:Mroh9 UTSW 1 162,888,251 (GRCm39) missense probably benign 0.00
R7052:Mroh9 UTSW 1 162,866,525 (GRCm39) missense possibly damaging 0.92
R7068:Mroh9 UTSW 1 162,866,750 (GRCm39) missense probably damaging 1.00
R7350:Mroh9 UTSW 1 162,903,858 (GRCm39) critical splice donor site probably null
R7545:Mroh9 UTSW 1 162,902,277 (GRCm39) missense possibly damaging 0.56
R7615:Mroh9 UTSW 1 162,873,601 (GRCm39) missense probably benign 0.40
R7743:Mroh9 UTSW 1 162,852,122 (GRCm39) missense probably benign
R7808:Mroh9 UTSW 1 162,866,678 (GRCm39) missense probably damaging 1.00
R8024:Mroh9 UTSW 1 162,866,802 (GRCm39) missense probably benign 0.02
R8062:Mroh9 UTSW 1 162,866,544 (GRCm39) missense probably damaging 1.00
R8145:Mroh9 UTSW 1 162,890,096 (GRCm39) missense probably benign 0.00
R8426:Mroh9 UTSW 1 162,852,294 (GRCm39) missense probably damaging 0.98
R8458:Mroh9 UTSW 1 162,883,250 (GRCm39) missense probably damaging 1.00
R8555:Mroh9 UTSW 1 162,899,595 (GRCm39) splice site probably null
R8960:Mroh9 UTSW 1 162,883,196 (GRCm39) missense probably benign 0.25
R9040:Mroh9 UTSW 1 162,890,069 (GRCm39) missense probably benign 0.06
R9125:Mroh9 UTSW 1 162,875,412 (GRCm39) missense probably benign 0.19
R9154:Mroh9 UTSW 1 162,890,030 (GRCm39) missense
R9596:Mroh9 UTSW 1 162,893,576 (GRCm39) missense probably damaging 0.98
R9612:Mroh9 UTSW 1 162,866,498 (GRCm39) missense probably damaging 1.00
RF003:Mroh9 UTSW 1 162,885,630 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAAGTGTAGCTATATCTTGAAGCTG -3'
(R):5'- AGTGTTCTTCTCCTACTTTAGAGG -3'

Sequencing Primer
(F):5'- AGCTGTAAAGATCTTGAAATACCAAC -3'
(R):5'- GATCCAGTGCAAACTTGTACCGTTG -3'
Posted On 2017-10-10