Incidental Mutation 'IGL02213:Mroh9'
ID 284758
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mroh9
Ensembl Gene ENSMUSG00000071890
Gene Name maestro heat-like repeat family member 9
Synonyms 4921528O07Rik, Armc11
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02213
Quality Score
Status
Chromosome 1
Chromosomal Location 162851871-162913239 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 162885648 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 328 (T328K)
Ref Sequence ENSEMBL: ENSMUSP00000094365 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096608]
AlphaFold G5E8L9
Predicted Effect probably damaging
Transcript: ENSMUST00000096608
AA Change: T328K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000094365
Gene: ENSMUSG00000071890
AA Change: T328K

DomainStartEndE-ValueType
SCOP:d1gw5b_ 231 716 2e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104420
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195132
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg1 G A 9: 54,523,254 (GRCm39) R458C probably damaging Het
Aldh6a1 T A 12: 84,479,326 (GRCm39) probably benign Het
Ankrd13a C T 5: 114,924,029 (GRCm39) R42W probably damaging Het
Arhgef17 T C 7: 100,539,633 (GRCm39) M73V probably benign Het
Borcs6 A G 11: 68,950,679 (GRCm39) E19G probably benign Het
Cacna2d2 C T 9: 107,391,247 (GRCm39) R425C probably damaging Het
Cap2 T A 13: 46,789,087 (GRCm39) probably benign Het
Ccdc146 C T 5: 21,521,902 (GRCm39) R374H probably benign Het
Cdk5rap2 A G 4: 70,235,839 (GRCm39) probably benign Het
Cyp3a57 A G 5: 145,318,090 (GRCm39) D357G probably damaging Het
Dleu7 C T 14: 62,514,404 (GRCm39) V193M probably benign Het
Dmxl1 T A 18: 50,010,741 (GRCm39) probably benign Het
Dnah7b T A 1: 46,272,752 (GRCm39) F2293L probably damaging Het
Fgf22 G T 10: 79,592,449 (GRCm39) V75L probably damaging Het
Fras1 C A 5: 96,793,730 (GRCm39) C1017* probably null Het
Frmd3 A C 4: 74,054,109 (GRCm39) I173L probably benign Het
Fst T C 13: 114,592,390 (GRCm39) N109S possibly damaging Het
Greb1 A G 12: 16,756,233 (GRCm39) L801P probably damaging Het
Ift88 A G 14: 57,715,502 (GRCm39) D515G probably damaging Het
Kcnh7 T C 2: 62,569,706 (GRCm39) D730G probably damaging Het
Mbd1 A T 18: 74,408,453 (GRCm39) I231F probably damaging Het
Mre11a T A 9: 14,723,180 (GRCm39) F358I probably damaging Het
Nostrin T C 2: 69,014,262 (GRCm39) L406P probably benign Het
Ntrk3 T A 7: 78,112,679 (GRCm39) Q159L probably benign Het
Oca2 T C 7: 55,971,232 (GRCm39) probably benign Het
Or4k49 A T 2: 111,495,020 (GRCm39) T150S probably benign Het
Or51af1 T A 7: 103,141,695 (GRCm39) H130L probably benign Het
Or5p54 T C 7: 107,554,511 (GRCm39) I221T probably damaging Het
Pfdn4 C T 2: 170,357,695 (GRCm39) Q21* probably null Het
Pkd1l3 T C 8: 110,357,977 (GRCm39) F823S probably damaging Het
Rnf212 C T 5: 108,895,276 (GRCm39) probably benign Het
Sbspon T C 1: 15,929,150 (GRCm39) S214G probably benign Het
Slc12a7 T C 13: 73,945,822 (GRCm39) probably null Het
Ugt3a1 A T 15: 9,370,310 (GRCm39) M485L probably benign Het
Vav1 T C 17: 57,612,351 (GRCm39) V561A possibly damaging Het
Vldlr A G 19: 27,218,726 (GRCm39) T485A probably benign Het
Wiz T C 17: 32,586,834 (GRCm39) T159A 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
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
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
Posted On 2015-04-16