Incidental Mutation 'R4034:Mroh9'
ID 313613
Institutional Source Beutler Lab
Gene Symbol Mroh9
Ensembl Gene ENSMUSG00000071890
Gene Name maestro heat-like repeat family member 9
Synonyms 4921528O07Rik, Armc11
MMRRC Submission 040962-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4034 (G1)
Quality Score 124
Status Not validated
Chromosome 1
Chromosomal Location 162851871-162913239 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 162908122 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000094365 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096608] [ENSMUST00000096608]
AlphaFold G5E8L9
Predicted Effect probably null
Transcript: ENSMUST00000096608
SMART Domains Protein: ENSMUSP00000094365
Gene: ENSMUSG00000071890

DomainStartEndE-ValueType
SCOP:d1gw5b_ 231 716 2e-8 SMART
Predicted Effect probably null
Transcript: ENSMUST00000096608
SMART Domains Protein: ENSMUSP00000094365
Gene: ENSMUSG00000071890

DomainStartEndE-ValueType
SCOP:d1gw5b_ 231 716 2e-8 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik2 A T 11: 48,910,108 (GRCm39) L775* probably null Het
Aarsd1 C T 11: 101,302,158 (GRCm39) V301I probably damaging Het
Arap1 A T 7: 101,049,484 (GRCm39) Y982F possibly damaging Het
Aspa T C 11: 73,199,597 (GRCm39) K227E possibly damaging Het
Ccdc168 A G 1: 44,098,026 (GRCm39) V1024A probably benign Het
Ccdc88c G A 12: 100,896,783 (GRCm39) A1389V possibly damaging Het
Cngb1 C A 8: 95,991,078 (GRCm39) C708F possibly damaging Het
Csn1s2a A G 5: 87,929,746 (GRCm39) Q115R probably benign Het
Cwf19l2 A T 9: 3,456,803 (GRCm39) H712L probably benign Het
Eml6 C A 11: 29,753,137 (GRCm39) V925L probably benign Het
Fbll1 G A 11: 35,688,505 (GRCm39) H253Y possibly damaging Het
Hmgcr C G 13: 96,787,571 (GRCm39) L852F probably damaging Het
Ltbp2 A T 12: 84,851,248 (GRCm39) C836S probably damaging Het
Muc5ac G A 7: 141,353,581 (GRCm39) probably null Het
Or2y1 A G 11: 49,386,287 (GRCm39) D309G possibly damaging Het
Pgm5 T A 19: 24,839,021 (GRCm39) I45F probably damaging Het
Ppl T C 16: 4,924,721 (GRCm39) T115A probably benign Het
Sgpp1 A G 12: 75,762,964 (GRCm39) Y406H probably damaging Het
Srsf4 C T 4: 131,627,413 (GRCm39) probably benign Het
St18 G A 1: 6,925,697 (GRCm39) probably null Het
Tcerg1 T A 18: 42,652,598 (GRCm39) N75K unknown Het
Tmco4 T C 4: 138,748,172 (GRCm39) Y251H probably damaging Het
Usp42 C T 5: 143,701,194 (GRCm39) S943N probably benign Het
Utp20 C T 10: 88,598,668 (GRCm39) V103I probably benign Het
Vmn1r14 G A 6: 57,211,310 (GRCm39) R252H possibly damaging Het
Wapl T C 14: 34,459,871 (GRCm39) V1013A possibly damaging Het
Zfp37 G A 4: 62,109,933 (GRCm39) T414I probably damaging Het
Zfp423 A G 8: 88,507,972 (GRCm39) C666R probably damaging 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
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
R6182:Mroh9 UTSW 1 162,893,612 (GRCm39) nonsense probably null
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'- ACAGATCCCCTGCCTTTGTC -3'
(R):5'- AACCTATGCTTAGTTTTGGACCTAC -3'

Sequencing Primer
(F):5'- AGATCCCCTGCCTTTGTCTCTTTG -3'
(R):5'- TTTGGACCTACAAAAACTAAAACGAC -3'
Posted On 2015-04-30