Incidental Mutation 'R7184:Cyp3a41a'
ID 559172
Institutional Source Beutler Lab
Gene Symbol Cyp3a41a
Ensembl Gene ENSMUSG00000075551
Gene Name cytochrome P450, family 3, subfamily a, polypeptide 41A
Synonyms steroid inducible, Cyp3a41
MMRRC Submission 045236-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.179) question?
Stock # R7184 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 145630859-145656946 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 145642663 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 232 (V232A)
Ref Sequence ENSEMBL: ENSMUSP00000091659 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094111]
AlphaFold Q9JMA7
Predicted Effect probably benign
Transcript: ENSMUST00000094111
AA Change: V232A

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000091659
Gene: ENSMUSG00000075551
AA Change: V232A

DomainStartEndE-ValueType
Pfam:p450 38 494 1.7e-136 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (63/63)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass A G 6: 23,094,219 (GRCm39) S500P possibly damaging Het
Aldh9a1 T A 1: 167,184,965 (GRCm39) N292K probably benign Het
Art2b A T 7: 101,229,658 (GRCm39) S80R probably benign Het
Atp6v1b2 G T 8: 69,555,219 (GRCm39) A194S possibly damaging Het
Bsnd T C 4: 106,349,109 (GRCm39) M44V probably damaging Het
Cadps2 A T 6: 23,583,428 (GRCm39) V383E probably benign Het
Cd93 T C 2: 148,284,459 (GRCm39) T296A possibly damaging Het
Cdk15 G T 1: 59,304,814 (GRCm39) E138D probably benign Het
Cdon A G 9: 35,375,191 (GRCm39) I406V probably benign Het
Cfhr4 A G 1: 139,660,822 (GRCm39) V622A possibly damaging Het
Dbndd1 T A 8: 124,235,860 (GRCm39) D130V probably damaging Het
Dnah14 C T 1: 181,532,094 (GRCm39) R2294* probably null Het
Eddm3b A G 14: 51,354,387 (GRCm39) Y125C probably damaging Het
Eif1ad14 G A 12: 87,886,492 (GRCm39) R46W possibly damaging Het
Enah A T 1: 181,749,957 (GRCm39) V294E probably damaging Het
Farp2 A G 1: 93,531,137 (GRCm39) E545G probably damaging Het
Farsb T C 1: 78,458,994 (GRCm39) E22G possibly damaging Het
Fcsk G A 8: 111,613,788 (GRCm39) P758S probably damaging Het
Fezf1 A G 6: 23,247,835 (GRCm39) V80A probably benign Het
Fpr2 T C 17: 18,113,533 (GRCm39) Y39H unknown Het
Fsd1l C A 4: 53,694,054 (GRCm39) R344S probably damaging Het
Fxyd1 G T 7: 30,751,401 (GRCm39) R90S unknown Het
Galnt4 T A 10: 98,944,466 (GRCm39) Y64N probably damaging Het
Gatb C T 3: 85,544,258 (GRCm39) Q409* probably null Het
Glipr2 A C 4: 43,968,667 (GRCm39) D73A possibly damaging Het
Gm40460 ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG 7: 141,794,450 (GRCm39) probably benign Het
Gpr88 C T 3: 116,045,643 (GRCm39) V223I possibly damaging Het
Gtf2h3 A G 5: 124,722,067 (GRCm39) N55S probably benign Het
Htr4 T A 18: 62,570,498 (GRCm39) C184* probably null Het
Ighv6-3 T A 12: 114,355,475 (GRCm39) R71S probably benign Het
Itpr2 G C 6: 146,212,585 (GRCm39) I1510M possibly damaging Het
Keap1 T C 9: 21,145,134 (GRCm39) Q292R probably benign Het
Mab21l4 T C 1: 93,082,237 (GRCm39) N294S probably benign Het
Malt1 A C 18: 65,580,764 (GRCm39) E219D probably benign Het
Manba T C 3: 135,228,915 (GRCm39) V279A possibly damaging Het
Map4k5 T A 12: 69,921,095 (GRCm39) H41L probably benign Het
Mcm2 T G 6: 88,868,776 (GRCm39) Y327S probably damaging Het
Nectin3 A G 16: 46,215,484 (GRCm39) I503T possibly damaging Het
Nqo1 T C 8: 108,119,279 (GRCm39) I99M probably damaging Het
Nrxn2 A G 19: 6,540,582 (GRCm39) H845R probably damaging Het
Otogl C T 10: 107,599,061 (GRCm39) C2254Y probably damaging Het
Pmm1 T C 15: 81,840,415 (GRCm39) N110S probably damaging Het
Poc1b G T 10: 98,970,199 (GRCm39) C68F probably benign Het
Polr1b A G 2: 128,965,842 (GRCm39) Y828C possibly damaging Het
Prl3d1 A G 13: 27,282,619 (GRCm39) H119R probably damaging Het
Pum3 A G 19: 27,403,412 (GRCm39) S30P probably benign Het
Rgl2 T C 17: 34,153,964 (GRCm39) F457L possibly damaging Het
Rusc1 T C 3: 88,999,194 (GRCm39) E196G possibly damaging Het
Sf3a3 A G 4: 124,608,772 (GRCm39) K29E probably benign Het
Slc13a1 A T 6: 24,092,311 (GRCm39) I475K probably damaging Het
Slc26a5 G T 5: 22,042,244 (GRCm39) Y237* probably null Het
Slc7a14 C T 3: 31,281,212 (GRCm39) G366D probably damaging Het
Tbc1d5 A G 17: 51,107,110 (GRCm39) V482A probably benign Het
Tdrd5 G T 1: 156,087,505 (GRCm39) Q883K probably benign Het
Tet2 T C 3: 133,179,391 (GRCm39) Y1258C probably damaging Het
Upf2 A G 2: 6,028,131 (GRCm39) D739G unknown Het
Vmn1r122 A T 7: 20,867,820 (GRCm39) F78L probably benign Het
Vmn1r75 A T 7: 11,614,915 (GRCm39) K216* probably null Het
Vmn2r11 A T 5: 109,201,281 (GRCm39) Y408N probably damaging Het
Wscd1 T A 11: 71,679,543 (GRCm39) V472D probably damaging Het
Zdbf2 G T 1: 63,345,664 (GRCm39) V1348F possibly damaging Het
Zfp442 G T 2: 150,250,056 (GRCm39) H615Q possibly damaging Het
Zfp457 C A 13: 67,442,065 (GRCm39) C170F possibly damaging Het
Zscan10 A G 17: 23,826,003 (GRCm39) probably null Het
Other mutations in Cyp3a41a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02284:Cyp3a41a APN 5 145,641,673 (GRCm39) splice site probably benign
IGL03003:Cyp3a41a APN 5 145,642,640 (GRCm39) missense probably benign
R0006:Cyp3a41a UTSW 5 145,641,606 (GRCm39) missense probably benign 0.01
R0515:Cyp3a41a UTSW 5 145,654,810 (GRCm39) missense probably damaging 1.00
R1052:Cyp3a41a UTSW 5 145,642,621 (GRCm39) missense possibly damaging 0.49
R3708:Cyp3a41a UTSW 5 145,654,733 (GRCm39) critical splice donor site probably null
R4049:Cyp3a41a UTSW 5 145,650,350 (GRCm39) missense probably damaging 1.00
R4755:Cyp3a41a UTSW 5 145,652,316 (GRCm39) missense probably damaging 1.00
R4975:Cyp3a41a UTSW 5 145,656,858 (GRCm39) start codon destroyed probably null 1.00
R6519:Cyp3a41a UTSW 5 145,652,308 (GRCm39) missense probably damaging 1.00
R6788:Cyp3a41a UTSW 5 145,642,639 (GRCm39) missense probably benign 0.00
R7372:Cyp3a41a UTSW 5 145,650,374 (GRCm39) missense possibly damaging 0.67
R7451:Cyp3a41a UTSW 5 145,636,550 (GRCm39) missense probably benign 0.10
R7463:Cyp3a41a UTSW 5 145,650,374 (GRCm39) missense probably damaging 1.00
R7766:Cyp3a41a UTSW 5 145,654,827 (GRCm39) missense probably damaging 0.99
R9179:Cyp3a41a UTSW 5 145,642,654 (GRCm39) missense probably benign
R9225:Cyp3a41a UTSW 5 145,650,414 (GRCm39) missense probably benign 0.03
R9300:Cyp3a41a UTSW 5 145,656,906 (GRCm39) start gained probably benign
R9308:Cyp3a41a UTSW 5 145,656,858 (GRCm39) start codon destroyed probably null 1.00
R9403:Cyp3a41a UTSW 5 145,639,008 (GRCm39) missense probably damaging 0.99
R9635:Cyp3a41a UTSW 5 145,652,320 (GRCm39) missense possibly damaging 0.95
R9682:Cyp3a41a UTSW 5 145,652,326 (GRCm39) missense possibly damaging 0.66
Predicted Primers PCR Primer
(F):5'- TTGTATCTTCCACTAGCACACAG -3'
(R):5'- GTCAGGTCGCAGATTTGGCTAC -3'

Sequencing Primer
(F):5'- AGCTTACATGTTCACAGCCC -3'
(R):5'- GTCGCAGATTTGGCTACTACACAG -3'
Posted On 2019-06-26