Incidental Mutation 'R1937:Cyp3a59'
ID 213532
Institutional Source Beutler Lab
Gene Symbol Cyp3a59
Ensembl Gene ENSMUSG00000061292
Gene Name cytochrome P450, family 3, subfamily a, polypeptide 59
Synonyms
MMRRC Submission 039955-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1937 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 146016067-146050097 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 146031187 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 117 (S117P)
Ref Sequence ENSEMBL: ENSMUSP00000049494 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035571] [ENSMUST00000199212]
AlphaFold D3Z2W7
Predicted Effect possibly damaging
Transcript: ENSMUST00000035571
AA Change: S117P

PolyPhen 2 Score 0.796 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000049494
Gene: ENSMUSG00000061292
AA Change: S117P

DomainStartEndE-ValueType
Pfam:p450 38 493 5.3e-128 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000199212
AA Change: S117P

PolyPhen 2 Score 0.490 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000142591
Gene: ENSMUSG00000061292
AA Change: S117P

DomainStartEndE-ValueType
signal peptide 1 29 N/A INTRINSIC
Pfam:p450 38 148 3.3e-20 PFAM
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 97.0%
  • 10x: 95.7%
  • 20x: 93.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730480H06Rik C A 5: 48,531,777 (GRCm39) T35K probably benign Het
Abhd14a A G 9: 106,317,446 (GRCm39) probably benign Het
Abhd8 A G 8: 71,914,506 (GRCm39) F41L possibly damaging Het
Ace2 A T X: 162,939,524 (GRCm39) M123L possibly damaging Het
Actr5 T C 2: 158,477,949 (GRCm39) Y440H possibly damaging Het
Akr1c6 T A 13: 4,496,383 (GRCm39) N81K probably benign Het
Aqp11 T A 7: 97,386,725 (GRCm39) N157I possibly damaging Het
Arhgap10 T C 8: 78,071,282 (GRCm39) E568G probably damaging Het
Asb7 T A 7: 66,329,001 (GRCm39) Q13L probably benign Het
Atf7ip C A 6: 136,537,778 (GRCm39) A345E probably benign Het
Atp8a2 T C 14: 60,097,719 (GRCm39) K770E probably benign Het
Bpifb4 A T 2: 153,785,996 (GRCm39) I259F probably damaging Het
Cand1 A T 10: 119,038,925 (GRCm39) D1218E probably damaging Het
Capg A G 6: 72,535,236 (GRCm39) probably null Het
Cep290 C T 10: 100,333,815 (GRCm39) T289M possibly damaging Het
Cfap69 T C 5: 5,643,818 (GRCm39) Y548C probably damaging Het
Cfap97d1 A T 11: 101,877,989 (GRCm39) H17L probably damaging Het
Cimip2b T A 4: 43,427,586 (GRCm39) K220N probably damaging Het
Clock A G 5: 76,377,340 (GRCm39) L652P probably damaging Het
Col3a1 C T 1: 45,373,453 (GRCm39) probably benign Het
Coro7 T C 16: 4,446,596 (GRCm39) E843G probably benign Het
Crebrf T C 17: 26,961,442 (GRCm39) S188P probably damaging Het
Crppa G A 12: 36,440,367 (GRCm39) V92I probably benign Het
Cul1 T C 6: 47,485,289 (GRCm39) F307L probably benign Het
Cyb561d2 G A 9: 107,417,515 (GRCm39) R79W probably damaging Het
Ddias A G 7: 92,507,830 (GRCm39) I695T probably benign Het
Dhx29 G A 13: 113,101,864 (GRCm39) G1311D probably benign Het
Dync2h1 A G 9: 7,139,159 (GRCm39) probably null Het
Ece2 T A 16: 20,436,616 (GRCm39) V146E probably damaging Het
Eml2 A G 7: 18,937,889 (GRCm39) K586E possibly damaging Het
Eps8l3 A G 3: 107,791,708 (GRCm39) E316G probably benign Het
Fam135b A T 15: 71,493,863 (GRCm39) L22H probably damaging Het
Focad T A 4: 88,319,318 (GRCm39) M1K probably null Het
Fryl A G 5: 73,290,710 (GRCm39) S65P probably damaging Het
Gm14190 C T 11: 99,581,556 (GRCm39) C4Y unknown Het
H2-T5 T A 17: 36,478,899 (GRCm39) T117S probably damaging Het
Ift74 T A 4: 94,550,883 (GRCm39) M345K probably benign Het
Jag1 C G 2: 136,925,393 (GRCm39) V1070L possibly damaging Het
Kcng1 T C 2: 168,104,941 (GRCm39) T302A probably benign Het
Kif20b T C 19: 34,930,278 (GRCm39) V1221A possibly damaging Het
Kif23 A T 9: 61,853,892 (GRCm39) probably null Het
Lpxn T G 19: 12,802,274 (GRCm39) S200A probably benign Het
Meiob A G 17: 25,037,305 (GRCm39) H61R probably benign Het
Mfhas1 C T 8: 36,056,799 (GRCm39) L425F probably damaging Het
Myo3a A T 2: 22,401,126 (GRCm39) S632C probably damaging Het
Naip2 T C 13: 100,298,362 (GRCm39) E558G probably benign Het
Naip2 C T 13: 100,298,368 (GRCm39) G556D probably benign Het
Nbeal1 T A 1: 60,307,100 (GRCm39) Y374* probably null Het
Notch3 T C 17: 32,372,826 (GRCm39) S582G probably benign Het
Nphs1 A T 7: 30,173,798 (GRCm39) Q985L probably damaging Het
Oas1c T A 5: 120,941,049 (GRCm39) H248L probably benign Het
Or5c1 A T 2: 37,221,896 (GRCm39) N46Y probably damaging Het
Or5g26 T C 2: 85,494,341 (GRCm39) I146V probably benign Het
Or5h25 A T 16: 58,930,157 (GRCm39) M272K probably benign Het
Or8g35 A G 9: 39,381,333 (GRCm39) S230P possibly damaging Het
Pamr1 A T 2: 102,472,617 (GRCm39) I639F possibly damaging Het
Panx1 G T 9: 14,918,980 (GRCm39) T293K possibly damaging Het
Papss1 G T 3: 131,305,632 (GRCm39) V226F probably benign Het
Pax1 G T 2: 147,209,809 (GRCm39) G301V possibly damaging Het
Pdlim5 C A 3: 141,950,742 (GRCm39) R557L possibly damaging Het
Pdyn C A 2: 129,531,729 (GRCm39) M20I probably benign Het
Pelp1 G A 11: 70,284,541 (GRCm39) probably null Het
Pkd2 T C 5: 104,626,790 (GRCm39) V324A probably damaging Het
Pkdrej A G 15: 85,703,368 (GRCm39) I856T probably benign Het
Polr1a T C 6: 71,913,536 (GRCm39) probably null Het
Pot1a A T 6: 25,753,323 (GRCm39) D404E probably benign Het
Ppp2r2a A T 14: 67,253,878 (GRCm39) I430N possibly damaging Het
Prob1 C T 18: 35,787,279 (GRCm39) R325Q possibly damaging Het
Prrc2a T C 17: 35,376,884 (GRCm39) D742G probably damaging Het
Psmc1 C T 12: 100,081,102 (GRCm39) P54S probably benign Het
Rab22a A G 2: 173,530,004 (GRCm39) T61A probably damaging Het
Rims1 T A 1: 22,358,754 (GRCm39) K184N probably damaging Het
Rnf213 G A 11: 119,322,511 (GRCm39) R1376H probably damaging Het
Ryr2 T C 13: 11,683,848 (GRCm39) E3072G probably damaging Het
Serpina1b T C 12: 103,698,420 (GRCm39) K143R probably benign Het
Slc22a15 T G 3: 101,787,505 (GRCm39) probably null Het
Slc25a14 G A X: 47,740,840 (GRCm39) V210I probably benign Het
Slc25a48 A C 13: 56,596,811 (GRCm39) T31P probably damaging Het
Slc9a3 C T 13: 74,314,175 (GRCm39) probably null Het
Slx4 T C 16: 3,805,030 (GRCm39) *105W probably null Het
Smc6 A G 12: 11,349,399 (GRCm39) N794S probably benign Het
Spata18 G A 5: 73,834,307 (GRCm39) R387Q probably damaging Het
Sphkap C A 1: 83,245,162 (GRCm39) E1486* probably null Het
Srsf6 C T 2: 162,776,403 (GRCm39) probably benign Het
St8sia1 C T 6: 142,909,398 (GRCm39) A33T probably damaging Het
Tet2 T C 3: 133,194,399 (GRCm39) T12A possibly damaging Het
Tmem144 G T 3: 79,732,611 (GRCm39) S222R probably damaging Het
Tnrc6c A G 11: 117,646,849 (GRCm39) D1450G possibly damaging Het
Top1 A T 2: 160,512,042 (GRCm39) K27N unknown Het
Tox2 A G 2: 163,067,476 (GRCm39) H30R probably benign Het
Tra2b T C 16: 22,065,993 (GRCm39) probably benign Het
Trio A T 15: 27,833,142 (GRCm39) V1165E probably damaging Het
Troap T A 15: 98,975,269 (GRCm39) S145R probably damaging Het
Ttc34 G A 4: 154,950,139 (GRCm39) A1031T possibly damaging Het
Ttc6 C T 12: 57,663,109 (GRCm39) P302S probably benign Het
Ubiad1 A G 4: 148,528,468 (GRCm39) L147P probably damaging Het
Ugt2b35 G T 5: 87,149,141 (GRCm39) V131F probably damaging Het
Utp25 A T 1: 192,804,401 (GRCm39) D200E probably damaging Het
Vmn1r167 G A 7: 23,204,452 (GRCm39) T188I probably benign Het
Vmn1r46 G T 6: 89,953,716 (GRCm39) M188I probably benign Het
Vmn2r115 T A 17: 23,578,388 (GRCm39) N620K probably damaging Het
Vmn2r66 A G 7: 84,644,344 (GRCm39) S689P probably damaging Het
Wipf2 C T 11: 98,783,236 (GRCm39) R221* probably null Het
Zbtb16 T C 9: 48,571,078 (GRCm39) S563G probably benign Het
Zfp319 T C 8: 96,055,199 (GRCm39) T335A probably damaging Het
Zfp418 A G 7: 7,185,401 (GRCm39) R455G possibly damaging Het
Other mutations in Cyp3a59
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01120:Cyp3a59 APN 5 146,039,671 (GRCm39) missense probably damaging 0.99
IGL01129:Cyp3a59 APN 5 146,035,089 (GRCm39) missense probably benign 0.06
IGL01628:Cyp3a59 APN 5 146,036,629 (GRCm39) missense possibly damaging 0.94
IGL01982:Cyp3a59 APN 5 146,041,545 (GRCm39) missense probably benign 0.00
IGL02094:Cyp3a59 APN 5 146,041,631 (GRCm39) missense probably benign 0.05
IGL02140:Cyp3a59 APN 5 146,039,690 (GRCm39) missense probably damaging 1.00
IGL02350:Cyp3a59 APN 5 146,016,152 (GRCm39) missense probably damaging 1.00
IGL02357:Cyp3a59 APN 5 146,016,152 (GRCm39) missense probably damaging 1.00
IGL02445:Cyp3a59 APN 5 146,033,463 (GRCm39) missense probably benign 0.00
IGL02681:Cyp3a59 APN 5 146,027,556 (GRCm39) splice site probably benign
IGL02870:Cyp3a59 APN 5 146,034,994 (GRCm39) missense probably benign
IGL03023:Cyp3a59 APN 5 146,022,660 (GRCm39) missense probably benign 0.02
PIT4802001:Cyp3a59 UTSW 5 146,039,611 (GRCm39) missense probably benign 0.00
R0220:Cyp3a59 UTSW 5 146,035,080 (GRCm39) missense probably benign 0.02
R0532:Cyp3a59 UTSW 5 146,033,463 (GRCm39) nonsense probably null
R1084:Cyp3a59 UTSW 5 146,033,484 (GRCm39) missense probably benign
R1263:Cyp3a59 UTSW 5 146,041,521 (GRCm39) missense probably damaging 1.00
R1573:Cyp3a59 UTSW 5 146,039,684 (GRCm39) missense probably damaging 1.00
R1747:Cyp3a59 UTSW 5 146,041,568 (GRCm39) missense probably benign
R1759:Cyp3a59 UTSW 5 146,035,060 (GRCm39) missense probably benign 0.10
R1812:Cyp3a59 UTSW 5 146,039,621 (GRCm39) missense probably damaging 1.00
R2026:Cyp3a59 UTSW 5 146,033,098 (GRCm39) missense probably damaging 1.00
R2060:Cyp3a59 UTSW 5 146,041,524 (GRCm39) missense probably damaging 1.00
R2355:Cyp3a59 UTSW 5 146,036,622 (GRCm39) missense probably benign 0.09
R3721:Cyp3a59 UTSW 5 146,033,407 (GRCm39) missense probably damaging 0.96
R4013:Cyp3a59 UTSW 5 146,016,193 (GRCm39) missense probably benign 0.01
R4421:Cyp3a59 UTSW 5 146,041,713 (GRCm39) splice site probably null
R4432:Cyp3a59 UTSW 5 146,041,596 (GRCm39) missense probably benign 0.04
R4633:Cyp3a59 UTSW 5 146,031,248 (GRCm39) missense probably damaging 1.00
R4843:Cyp3a59 UTSW 5 146,033,071 (GRCm39) missense possibly damaging 0.61
R4886:Cyp3a59 UTSW 5 146,024,197 (GRCm39) missense probably damaging 1.00
R5236:Cyp3a59 UTSW 5 146,039,635 (GRCm39) missense probably benign 0.20
R5386:Cyp3a59 UTSW 5 146,022,578 (GRCm39) missense probably benign 0.01
R5627:Cyp3a59 UTSW 5 146,049,664 (GRCm39) missense probably benign 0.00
R5792:Cyp3a59 UTSW 5 146,036,661 (GRCm39) missense possibly damaging 0.92
R5935:Cyp3a59 UTSW 5 146,027,455 (GRCm39) nonsense probably null
R6531:Cyp3a59 UTSW 5 146,035,027 (GRCm39) missense probably benign 0.00
R6790:Cyp3a59 UTSW 5 146,033,143 (GRCm39) missense probably benign
R7108:Cyp3a59 UTSW 5 146,033,143 (GRCm39) missense probably benign
R7222:Cyp3a59 UTSW 5 146,033,385 (GRCm39) critical splice acceptor site probably null
R7447:Cyp3a59 UTSW 5 146,024,215 (GRCm39) missense probably benign 0.25
R7457:Cyp3a59 UTSW 5 146,041,560 (GRCm39) missense probably damaging 1.00
R7723:Cyp3a59 UTSW 5 146,016,154 (GRCm39) missense probably benign 0.06
R8171:Cyp3a59 UTSW 5 146,022,584 (GRCm39) missense probably damaging 1.00
R8417:Cyp3a59 UTSW 5 146,027,495 (GRCm39) missense possibly damaging 0.49
R8474:Cyp3a59 UTSW 5 146,041,487 (GRCm39) missense probably benign 0.01
R8716:Cyp3a59 UTSW 5 146,033,411 (GRCm39) missense probably damaging 0.99
R8728:Cyp3a59 UTSW 5 146,035,122 (GRCm39) critical splice donor site probably null
R8839:Cyp3a59 UTSW 5 146,045,896 (GRCm39) missense probably benign
R8969:Cyp3a59 UTSW 5 146,049,630 (GRCm39) missense probably benign 0.15
R9478:Cyp3a59 UTSW 5 146,034,997 (GRCm39) missense probably damaging 0.98
R9697:Cyp3a59 UTSW 5 146,031,190 (GRCm39) missense probably damaging 0.99
R9705:Cyp3a59 UTSW 5 146,033,120 (GRCm39) missense probably benign 0.00
Z1088:Cyp3a59 UTSW 5 146,035,032 (GRCm39) missense probably benign 0.33
Predicted Primers PCR Primer
(F):5'- AGCTGTGACAGATGGATAGATATCAC -3'
(R):5'- TCATAGGATCGACCCTTGGAAAG -3'

Sequencing Primer
(F):5'- GAACATCTAGTAAGACCCAGAC -3'
(R):5'- CCTTGGAAAGGGTCTCTTGG -3'
Posted On 2014-07-14