Incidental Mutation 'R4280:Mtres1'
ID 322853
Institutional Source Beutler Lab
Gene Symbol Mtres1
Ensembl Gene ENSMUSG00000019797
Gene Name mitochondrial transcription rescue factor 1
Synonyms 1700021F05Rik
MMRRC Submission 041648-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.137) question?
Stock # R4280 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 43401129-43416990 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 43408905 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 79 (F79L)
Ref Sequence ENSEMBL: ENSMUSP00000119053 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000147196]
AlphaFold Q9CQF4
Predicted Effect probably benign
Transcript: ENSMUST00000019932
AA Change: F79L

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000019932
Gene: ENSMUSG00000019797
AA Change: F79L

DomainStartEndE-ValueType
low complexity region 84 96 N/A INTRINSIC
low complexity region 100 125 N/A INTRINSIC
Blast:S4 142 212 4e-37 BLAST
low complexity region 229 240 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126463
Predicted Effect probably benign
Transcript: ENSMUST00000147196
AA Change: F79L

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000119053
Gene: ENSMUSG00000019797
AA Change: F79L

DomainStartEndE-ValueType
low complexity region 84 96 N/A INTRINSIC
low complexity region 100 125 N/A INTRINSIC
Blast:S4 142 188 1e-19 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216546
Meta Mutation Damage Score 0.0728 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 100% (51/51)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap32 T C 9: 32,171,185 (GRCm39) C1322R probably damaging Het
Arl6ip1 AAAATAAATAAATAAATAAATAAATA AAAATAAATAAATAAATAAATAAATAAATA 7: 117,721,122 (GRCm39) probably benign Het
Arvcf G A 16: 18,216,741 (GRCm39) R292H probably damaging Het
Ccdc102a C A 8: 95,634,444 (GRCm39) G382* probably null Het
Cd274 A T 19: 29,357,871 (GRCm39) M188L probably benign Het
Cep76 T A 18: 67,773,229 (GRCm39) D23V probably benign Het
Cimip3 T C 17: 47,724,780 (GRCm39) M17V probably benign Het
Clec12a A G 6: 129,340,892 (GRCm39) Y224C probably damaging Het
Cplx2 A G 13: 54,527,377 (GRCm39) E87G probably damaging Het
Ctr9 A G 7: 110,645,930 (GRCm39) probably benign Het
Dgat2 A G 7: 98,808,204 (GRCm39) I157T probably damaging Het
Epha1 G T 6: 42,341,986 (GRCm39) P355T probably damaging Het
Fabp3 C T 4: 130,206,245 (GRCm39) probably null Het
Gmip T A 8: 70,266,251 (GRCm39) probably benign Het
Hephl1 A G 9: 15,023,330 (GRCm39) V24A probably benign Het
Itgb4 T A 11: 115,881,761 (GRCm39) M771K probably damaging Het
Mov10 A C 3: 104,707,095 (GRCm39) F635V probably damaging Het
Or10ag60 A G 2: 87,438,595 (GRCm39) T288A possibly damaging Het
Or5an9 A G 19: 12,187,302 (GRCm39) Y124C probably damaging Het
Pbrm1 T C 14: 30,829,269 (GRCm39) probably null Het
Plscr1l1 T C 9: 92,225,701 (GRCm39) Y8H possibly damaging Het
Plxnd1 C A 6: 115,933,055 (GRCm39) probably benign Het
Plxnd1 A T 6: 115,933,056 (GRCm39) probably null Het
Pnma5 T C X: 72,079,036 (GRCm39) M549V probably benign Het
Polq C A 16: 36,902,419 (GRCm39) Q2205K probably damaging Het
Ppp4r3c1 A T X: 88,976,105 (GRCm39) W31R probably damaging Het
Pramel24 A G 4: 143,452,592 (GRCm39) T8A possibly damaging Het
Psma8 T A 18: 14,854,292 (GRCm39) D57E probably benign Het
Rbm47 T C 5: 66,183,520 (GRCm39) Y361C probably damaging Het
Rec8 A G 14: 55,856,091 (GRCm39) H11R probably damaging Het
Ric1 A G 19: 29,563,950 (GRCm39) Y568C probably damaging Het
Rrp36 G A 17: 46,983,302 (GRCm39) T104I probably damaging Het
Rrs1 G A 1: 9,616,364 (GRCm39) G206S probably damaging Het
Scgb2b6 A G 7: 31,318,367 (GRCm39) noncoding transcript Het
Skint5 T A 4: 113,799,749 (GRCm39) K126I probably damaging Het
Slc38a10 C T 11: 120,028,704 (GRCm39) G202D probably damaging Het
Supt5 G A 7: 28,016,498 (GRCm39) R761W probably damaging Het
Tmtc2 A G 10: 105,184,294 (GRCm39) probably null Het
Tob1 T C 11: 94,105,148 (GRCm39) V228A probably benign Het
Traj44 T C 14: 54,411,148 (GRCm39) probably benign Het
Trps1 G A 15: 50,709,478 (GRCm39) L291F probably benign Het
Ttn T A 2: 76,585,168 (GRCm39) I22042F probably damaging Het
Ush2a A G 1: 188,310,658 (GRCm39) Q2078R probably benign Het
Zbtb24 T C 10: 41,340,916 (GRCm39) S649P probably benign Het
Zfp28 A T 7: 6,396,700 (GRCm39) Q378H probably benign Het
Zfp429 A C 13: 67,538,914 (GRCm39) C177G probably damaging Het
Other mutations in Mtres1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1531:Mtres1 UTSW 10 43,401,316 (GRCm39) missense probably benign 0.01
R2497:Mtres1 UTSW 10 43,401,263 (GRCm39) unclassified probably benign
R4574:Mtres1 UTSW 10 43,409,006 (GRCm39) missense probably damaging 1.00
R5460:Mtres1 UTSW 10 43,408,861 (GRCm39) missense probably benign 0.07
R5782:Mtres1 UTSW 10 43,408,899 (GRCm39) missense probably benign 0.05
R6103:Mtres1 UTSW 10 43,408,916 (GRCm39) missense probably benign 0.08
R6850:Mtres1 UTSW 10 43,408,721 (GRCm39) small deletion probably benign
R6866:Mtres1 UTSW 10 43,408,721 (GRCm39) small deletion probably benign
R6867:Mtres1 UTSW 10 43,408,721 (GRCm39) small deletion probably benign
R6899:Mtres1 UTSW 10 43,408,780 (GRCm39) missense possibly damaging 0.47
R7997:Mtres1 UTSW 10 43,401,356 (GRCm39) missense probably benign 0.00
R8483:Mtres1 UTSW 10 43,408,915 (GRCm39) missense probably benign 0.17
R8676:Mtres1 UTSW 10 43,408,933 (GRCm39) missense probably benign 0.14
R8990:Mtres1 UTSW 10 43,401,233 (GRCm39) missense unknown
X0022:Mtres1 UTSW 10 43,401,379 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAAAGACTGCACCACCTTTTCC -3'
(R):5'- CACAGGTGCTCTAAGGAAGC -3'

Sequencing Primer
(F):5'- CAGGTCTTTGTAGTCCTTCGC -3'
(R):5'- CTCTAAGGAAGCCAGATGCCTG -3'
Posted On 2015-06-20