Incidental Mutation 'R9728:Miox'
ID 731181
Institutional Source Beutler Lab
Gene Symbol Miox
Ensembl Gene ENSMUSG00000022613
Gene Name myo-inositol oxygenase
Synonyms RSOR, C85427, 0610009I10Rik, Aldrl6
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.158) question?
Stock # R9728 (G1)
Quality Score 225.009
Status Not validated
Chromosome 15
Chromosomal Location 89218676-89221210 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 89218703 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000023282]
AlphaFold Q9QXN5
Predicted Effect probably benign
Transcript: ENSMUST00000023282
SMART Domains Protein: ENSMUSP00000023282
Gene: ENSMUSG00000022613

DomainStartEndE-ValueType
Pfam:MIOX 31 285 2.1e-125 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000162033
SMART Domains Protein: ENSMUSP00000123732
Gene: ENSMUSG00000022613

DomainStartEndE-ValueType
Pfam:MIOX 1 53 7.2e-20 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atr G A 9: 95,797,050 (GRCm39) A1698T probably benign Het
Caml T A 13: 55,779,670 (GRCm39) S248T possibly damaging Het
Copg1 A G 6: 87,879,225 (GRCm39) I424V probably damaging Het
Cwh43 A T 5: 73,565,629 (GRCm39) N65Y possibly damaging Het
Defb1 A G 8: 22,284,486 (GRCm39) Y35C probably damaging Het
Disc1 A T 8: 125,959,795 (GRCm39) E769V probably null Het
Egln1 G A 8: 125,675,093 (GRCm39) T234I possibly damaging Het
Esco2 A T 14: 66,069,069 (GRCm39) F80L probably benign Het
Frem2 C T 3: 53,564,052 (GRCm39) A152T probably benign Het
Gcc1 T C 6: 28,420,544 (GRCm39) R258G probably damaging Het
Gm19410 A G 8: 36,247,594 (GRCm39) T469A possibly damaging Het
Gm4884 A T 7: 40,692,689 (GRCm39) Q219H probably benign Het
Gpr160 A G 3: 30,950,144 (GRCm39) N72S probably damaging Het
Hps3 C A 3: 20,065,128 (GRCm39) A771S probably benign Het
Igkv12-46 G T 6: 69,741,967 (GRCm39) P4T possibly damaging Het
Iqcf5 A T 9: 106,393,168 (GRCm39) I142L probably damaging Het
Kcna10 A T 3: 107,101,513 (GRCm39) N48I possibly damaging Het
Klhdc9 A G 1: 171,187,357 (GRCm39) S214P probably damaging Het
Knop1 C T 7: 118,451,840 (GRCm39) S293N Het
Lgr6 A G 1: 134,915,245 (GRCm39) L778P probably damaging Het
Lrrk2 A G 15: 91,618,228 (GRCm39) N909S probably benign Het
Mcm5 C T 8: 75,844,168 (GRCm39) S313F probably benign Het
Mei1 G A 15: 81,966,098 (GRCm39) G240D Het
Myo1e A G 9: 70,223,924 (GRCm39) Y128C probably damaging Het
Nlrp9a T A 7: 26,256,915 (GRCm39) Y178N probably damaging Het
Or14a259 A G 7: 86,012,771 (GRCm39) L258P probably damaging Het
Or5m13 A G 2: 85,748,887 (GRCm39) N206S possibly damaging Het
Or8u8 A T 2: 86,011,636 (GRCm39) M273K possibly damaging Het
Pde11a C A 2: 76,121,608 (GRCm39) L324F probably damaging Het
Pprc1 T C 19: 46,060,639 (GRCm39) V1568A probably damaging Het
Ralgps1 C T 2: 33,163,626 (GRCm39) V144M probably damaging Het
Rgs22 A T 15: 36,040,856 (GRCm39) V1001E probably benign Het
Sapcd2 C A 2: 25,262,669 (GRCm39) A76D probably damaging Het
Sec24b A G 3: 129,790,422 (GRCm39) I701T probably damaging Het
Sema4a T C 3: 88,348,187 (GRCm39) probably null Het
Setd5 G T 6: 113,128,366 (GRCm39) V1440L probably benign Het
Sik3 A G 9: 46,106,142 (GRCm39) K337E possibly damaging Het
Slc14a1 C A 18: 78,152,807 (GRCm39) A367S probably damaging Het
Slc23a2 G T 2: 131,900,130 (GRCm39) N568K probably damaging Het
Spag16 A G 1: 69,962,842 (GRCm39) R330G probably benign Het
Sspo G A 6: 48,432,707 (GRCm39) G861D probably damaging Het
Sun5 T A 2: 153,709,466 (GRCm39) M75L probably benign Het
Syde1 AGCCCGAAAACACGGGGCTCTGC AGC 10: 78,424,638 (GRCm39) probably null Het
Synrg A G 11: 83,915,117 (GRCm39) Y963C probably damaging Het
Tdpoz6 A T 3: 93,599,807 (GRCm39) C187* probably null Het
Trbv15 A T 6: 41,118,550 (GRCm39) E102V possibly damaging Het
Trim43b G T 9: 88,973,395 (GRCm39) H113N probably benign Het
Trrap G T 5: 144,726,193 (GRCm39) D381Y probably benign Het
Tubb6 A G 18: 67,534,671 (GRCm39) H190R probably benign Het
Unc45a G T 7: 79,978,448 (GRCm39) L667I probably benign Het
Vav1 A G 17: 57,612,459 (GRCm39) D570G probably benign Het
Vmn1r214 T C 13: 23,219,007 (GRCm39) V167A probably benign Het
Vmn2r112 G A 17: 22,824,108 (GRCm39) M454I probably damaging Het
Vwf C A 6: 125,568,670 (GRCm39) L398I possibly damaging Het
Zfp13 C T 17: 23,799,788 (GRCm39) R107K possibly damaging Het
Zfp318 G A 17: 46,707,713 (GRCm39) R257Q probably benign Het
Zfp9 G T 6: 118,443,851 (GRCm39) A58E probably benign Het
Other mutations in Miox
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03070:Miox APN 15 89,220,287 (GRCm39) missense possibly damaging 0.48
R0001:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0011:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0011:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0039:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0043:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0079:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0081:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0109:Miox UTSW 15 89,219,784 (GRCm39) missense probably benign 0.17
R0109:Miox UTSW 15 89,219,784 (GRCm39) missense probably benign 0.17
R0134:Miox UTSW 15 89,218,657 (GRCm39) unclassified probably benign
R0166:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0172:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0173:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0225:Miox UTSW 15 89,218,657 (GRCm39) unclassified probably benign
R0284:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0285:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0288:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R0681:Miox UTSW 15 89,220,477 (GRCm39) missense possibly damaging 0.48
R1383:Miox UTSW 15 89,219,245 (GRCm39) missense probably damaging 1.00
R4620:Miox UTSW 15 89,220,324 (GRCm39) missense probably benign 0.43
R5016:Miox UTSW 15 89,219,767 (GRCm39) missense probably null 1.00
R5110:Miox UTSW 15 89,219,759 (GRCm39) missense probably benign
R5393:Miox UTSW 15 89,220,450 (GRCm39) nonsense probably null
R6136:Miox UTSW 15 89,219,524 (GRCm39) missense probably damaging 1.00
R6339:Miox UTSW 15 89,219,702 (GRCm39) nonsense probably null
R7309:Miox UTSW 15 89,220,252 (GRCm39) missense probably damaging 1.00
R7402:Miox UTSW 15 89,219,206 (GRCm39) missense probably benign 0.01
R7891:Miox UTSW 15 89,220,742 (GRCm39) missense probably benign 0.10
R7913:Miox UTSW 15 89,220,785 (GRCm39) missense probably damaging 0.99
R9136:Miox UTSW 15 89,220,740 (GRCm39) missense probably damaging 1.00
R9660:Miox UTSW 15 89,218,703 (GRCm39) unclassified probably benign
R9711:Miox UTSW 15 89,220,785 (GRCm39) missense probably damaging 0.99
Z1177:Miox UTSW 15 89,219,847 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TAACTTGCTGAGGTCAGGAGG -3'
(R):5'- TGCTGATCTCCTTGCATTTAGAAG -3'

Sequencing Primer
(F):5'- GAAGGAGCATGGTCACTTATTAC -3'
(R):5'- CGGTTGCCTGATTCAACAAG -3'
Posted On 2022-10-06