Incidental Mutation 'IGL01348:Cyp3a11'
ID 75131
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp3a11
Ensembl Gene ENSMUSG00000056035
Gene Name cytochrome P450, family 3, subfamily a, polypeptide 11
Synonyms Cyp3a, Pcn, IIIAm1
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01348
Quality Score
Status
Chromosome 5
Chromosomal Location 145791417-145816664 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 145805817 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 157 (V157E)
Ref Sequence ENSEMBL: ENSMUSP00000037665 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035918]
AlphaFold Q64459
Predicted Effect possibly damaging
Transcript: ENSMUST00000035918
AA Change: V157E

PolyPhen 2 Score 0.804 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000037665
Gene: ENSMUSG00000056035
AA Change: V157E

DomainStartEndE-ValueType
Pfam:p450 38 494 2.4e-136 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199857
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700093K21Rik T C 11: 23,467,213 (GRCm39) E140G probably null Het
Adgrl3 A G 5: 81,874,570 (GRCm39) T956A probably damaging Het
Aff4 G A 11: 53,293,327 (GRCm39) S772N probably benign Het
Ark2n A G 18: 77,761,613 (GRCm39) I233T possibly damaging Het
Atad5 A G 11: 79,986,390 (GRCm39) I492M probably benign Het
Atf4 T C 15: 80,140,728 (GRCm39) probably benign Het
Atrip A G 9: 108,898,363 (GRCm39) S219P probably damaging Het
Axl G A 7: 25,462,734 (GRCm39) R656W probably damaging Het
B3gnt3 T A 8: 72,145,648 (GRCm39) Q240L possibly damaging Het
Baz2b A G 2: 59,764,031 (GRCm39) V915A possibly damaging Het
Cacna1s T C 1: 136,002,890 (GRCm39) V329A possibly damaging Het
Celf3 C A 3: 94,395,535 (GRCm39) Q388K possibly damaging Het
Ciita T C 16: 10,328,591 (GRCm39) S292P probably damaging Het
Cip2a A G 16: 48,833,551 (GRCm39) I551V probably damaging Het
Clec18a G A 8: 111,798,245 (GRCm39) A423V probably damaging Het
Clnk T C 5: 38,870,550 (GRCm39) D336G probably damaging Het
Csmd1 T G 8: 15,960,596 (GRCm39) H3273P probably damaging Het
Dcp1b T C 6: 119,160,679 (GRCm39) I87T probably damaging Het
Ell3 A G 2: 121,272,277 (GRCm39) S66P probably damaging Het
Ercc4 T C 16: 12,950,798 (GRCm39) F631L probably damaging Het
Etl4 T A 2: 20,811,784 (GRCm39) V1289D probably damaging Het
Gm16372 T C 12: 24,543,606 (GRCm39) probably benign Het
Gm4553 C T 7: 141,718,909 (GRCm39) C173Y unknown Het
Gvin-ps5 T A 7: 105,929,042 (GRCm39) H285L unknown Het
Gykl1 A T 18: 52,827,808 (GRCm39) I339F possibly damaging Het
H60b A C 10: 22,162,078 (GRCm39) N101T possibly damaging Het
Inpp4a C T 1: 37,427,986 (GRCm39) T407I probably damaging Het
Itga11 A G 9: 62,651,861 (GRCm39) N331S possibly damaging Het
Kbtbd6 T A 14: 79,690,783 (GRCm39) C430S probably damaging Het
Mfsd4a T C 1: 131,995,564 (GRCm39) S1G probably null Het
Mybpc2 C A 7: 44,165,352 (GRCm39) M372I probably benign Het
Myh10 A T 11: 68,702,629 (GRCm39) T1768S probably benign Het
Myh8 A G 11: 67,188,606 (GRCm39) K1063E probably damaging Het
Nat8f5 A T 6: 85,794,862 (GRCm39) F33I probably damaging Het
Nbeal2 T G 9: 110,458,214 (GRCm39) N2119T probably damaging Het
Nek11 C T 9: 105,270,112 (GRCm39) G37S probably damaging Het
Npc1l1 T C 11: 6,177,974 (GRCm39) N479D probably damaging Het
Nup160 A G 2: 90,530,772 (GRCm39) T477A probably benign Het
Or10al5 A T 17: 38,063,177 (GRCm39) H144L probably benign Het
Or5h18 T A 16: 58,848,157 (GRCm39) T38S probably damaging Het
Pcgf2 A G 11: 97,581,066 (GRCm39) V259A probably benign Het
Pmm1 A G 15: 81,836,219 (GRCm39) V131A probably damaging Het
Polr3a A T 14: 24,511,831 (GRCm39) D908E probably damaging Het
Psg29 A C 7: 16,944,598 (GRCm39) R369S probably benign Het
Ptprq T A 10: 107,547,765 (GRCm39) D211V probably damaging Het
Rdh9 A G 10: 127,612,661 (GRCm39) N103S probably benign Het
Riok3 T C 18: 12,286,020 (GRCm39) probably benign Het
Serpinb1b A T 13: 33,275,398 (GRCm39) Q174H probably benign Het
Sgip1 G T 4: 102,772,353 (GRCm39) probably null Het
Sgpp1 A T 12: 75,781,767 (GRCm39) Y191N probably damaging Het
Slc12a1 A G 2: 125,036,051 (GRCm39) N641S probably damaging Het
Slc5a4b T C 10: 75,906,422 (GRCm39) N399S probably damaging Het
Snx16 C T 3: 10,484,219 (GRCm39) A335T probably damaging Het
Sos2 C T 12: 69,664,866 (GRCm39) R355H probably damaging Het
Szt2 A G 4: 118,250,821 (GRCm39) probably benign Het
Tbcd T A 11: 121,387,902 (GRCm39) D344E probably benign Het
Tek C A 4: 94,747,895 (GRCm39) Q988K probably damaging Het
Tgm6 A G 2: 129,979,299 (GRCm39) D143G probably damaging Het
Tpx2 A G 2: 152,735,511 (GRCm39) K713R probably damaging Het
Trappc9 T A 15: 72,808,858 (GRCm39) E556V possibly damaging Het
Trpm6 A T 19: 18,855,015 (GRCm39) K1891N probably damaging Het
Trpv1 G A 11: 73,129,078 (GRCm39) probably null Het
Usp37 T C 1: 74,500,861 (GRCm39) S567G probably damaging Het
Zfp773 A T 7: 7,138,314 (GRCm39) V107D possibly damaging Het
Other mutations in Cyp3a11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00848:Cyp3a11 APN 5 145,799,275 (GRCm39) missense probably damaging 1.00
IGL01316:Cyp3a11 APN 5 145,791,961 (GRCm39) missense possibly damaging 0.78
IGL01591:Cyp3a11 APN 5 145,812,291 (GRCm39) splice site probably benign
IGL01665:Cyp3a11 APN 5 145,805,475 (GRCm39) missense probably benign 0.00
IGL02203:Cyp3a11 APN 5 145,805,976 (GRCm39) missense probably damaging 1.00
IGL02894:Cyp3a11 APN 5 145,805,836 (GRCm39) nonsense probably null
IGL03201:Cyp3a11 APN 5 145,797,189 (GRCm39) missense possibly damaging 0.94
IGL03342:Cyp3a11 APN 5 145,791,927 (GRCm39) missense probably damaging 0.96
PIT4486001:Cyp3a11 UTSW 5 145,797,302 (GRCm39) missense probably damaging 0.99
R0347:Cyp3a11 UTSW 5 145,802,735 (GRCm39) missense possibly damaging 0.93
R0376:Cyp3a11 UTSW 5 145,799,262 (GRCm39) nonsense probably null
R0378:Cyp3a11 UTSW 5 145,805,417 (GRCm39) missense probably benign 0.43
R0448:Cyp3a11 UTSW 5 145,799,204 (GRCm39) missense probably benign 0.00
R0567:Cyp3a11 UTSW 5 145,805,959 (GRCm39) missense probably damaging 1.00
R0968:Cyp3a11 UTSW 5 145,799,324 (GRCm39) splice site probably benign
R1292:Cyp3a11 UTSW 5 145,802,804 (GRCm39) missense probably benign 0.04
R1400:Cyp3a11 UTSW 5 145,799,299 (GRCm39) missense probably damaging 0.98
R1478:Cyp3a11 UTSW 5 145,795,581 (GRCm39) missense probably benign 0.01
R1520:Cyp3a11 UTSW 5 145,799,263 (GRCm39) missense probably damaging 1.00
R1716:Cyp3a11 UTSW 5 145,805,776 (GRCm39) missense probably benign
R2060:Cyp3a11 UTSW 5 145,791,891 (GRCm39) missense probably benign 0.00
R2076:Cyp3a11 UTSW 5 145,816,576 (GRCm39) missense probably benign
R2227:Cyp3a11 UTSW 5 145,805,357 (GRCm39) missense possibly damaging 0.90
R3725:Cyp3a11 UTSW 5 145,802,810 (GRCm39) missense probably benign 0.02
R4222:Cyp3a11 UTSW 5 145,797,276 (GRCm39) missense probably damaging 0.99
R4256:Cyp3a11 UTSW 5 145,806,005 (GRCm39) missense probably benign 0.04
R4294:Cyp3a11 UTSW 5 145,806,005 (GRCm39) missense probably benign 0.04
R4852:Cyp3a11 UTSW 5 145,797,305 (GRCm39) missense probably damaging 1.00
R5229:Cyp3a11 UTSW 5 145,791,945 (GRCm39) missense probably benign 0.00
R5285:Cyp3a11 UTSW 5 145,791,893 (GRCm39) missense probably benign 0.00
R5590:Cyp3a11 UTSW 5 145,802,787 (GRCm39) missense probably benign 0.00
R5703:Cyp3a11 UTSW 5 145,797,183 (GRCm39) missense probably benign
R5786:Cyp3a11 UTSW 5 145,799,284 (GRCm39) missense possibly damaging 0.47
R6291:Cyp3a11 UTSW 5 145,799,237 (GRCm39) missense possibly damaging 0.89
R6405:Cyp3a11 UTSW 5 145,799,230 (GRCm39) missense probably damaging 0.96
R6892:Cyp3a11 UTSW 5 145,797,258 (GRCm39) missense probably damaging 0.98
R7114:Cyp3a11 UTSW 5 145,795,593 (GRCm39) missense probably benign 0.16
R7243:Cyp3a11 UTSW 5 145,795,613 (GRCm39) missense probably damaging 0.96
R7438:Cyp3a11 UTSW 5 145,802,710 (GRCm39) missense probably benign 0.39
R7611:Cyp3a11 UTSW 5 145,797,191 (GRCm39) missense probably benign 0.25
R8346:Cyp3a11 UTSW 5 145,795,612 (GRCm39) missense probably damaging 1.00
R8371:Cyp3a11 UTSW 5 145,805,438 (GRCm39) missense possibly damaging 0.92
R8895:Cyp3a11 UTSW 5 145,797,330 (GRCm39) missense probably benign
R9043:Cyp3a11 UTSW 5 145,805,995 (GRCm39) missense probably benign 0.02
R9300:Cyp3a11 UTSW 5 145,799,164 (GRCm39) missense possibly damaging 0.60
R9404:Cyp3a11 UTSW 5 145,799,258 (GRCm39) missense probably benign 0.40
Posted On 2013-10-07