Incidental Mutation 'R1462:Cyp2c38'
ID 158993
Institutional Source Beutler Lab
Gene Symbol Cyp2c38
Ensembl Gene ENSMUSG00000032808
Gene Name cytochrome P450, family 2, subfamily c, polypeptide 38
Synonyms
MMRRC Submission 039516-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # R1462 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 39379109-39451519 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 39380632 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 418 (N418D)
Ref Sequence ENSEMBL: ENSMUSP00000044722 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035488]
AlphaFold P56655
Predicted Effect probably damaging
Transcript: ENSMUST00000035488
AA Change: N418D

PolyPhen 2 Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000044722
Gene: ENSMUSG00000032808
AA Change: N418D

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:p450 30 487 1.5e-161 PFAM
Meta Mutation Damage Score 0.1494 question?
Coding Region Coverage
  • 1x: 98.7%
  • 3x: 97.4%
  • 10x: 92.6%
  • 20x: 79.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930433I11Rik C A 7: 40,642,370 (GRCm39) S104* probably null Het
Abca9 T C 11: 110,051,342 (GRCm39) D118G probably benign Het
Adamts16 A G 13: 70,984,253 (GRCm39) F137L probably benign Het
Adamts3 T C 5: 90,009,208 (GRCm39) I152V probably benign Het
Adcy4 T A 14: 56,015,765 (GRCm39) E441D possibly damaging Het
Adgra1 T A 7: 139,455,745 (GRCm39) Y458N probably damaging Het
Bhlhe22 C G 3: 18,109,946 (GRCm39) S332C probably damaging Het
Card19 T A 13: 49,358,760 (GRCm39) Q71L probably benign Het
Ccdc12 T C 9: 110,485,662 (GRCm39) L11P probably damaging Het
Cdadc1 A G 14: 59,813,307 (GRCm39) Y367H probably damaging Het
Cdc5l G T 17: 45,719,288 (GRCm39) Q542K possibly damaging Het
Cep170 T C 1: 176,584,211 (GRCm39) K723E possibly damaging Het
Cep70 A G 9: 99,145,773 (GRCm39) I147V probably benign Het
Cfap58 A T 19: 47,950,869 (GRCm39) H410L probably damaging Het
Chat T C 14: 32,142,735 (GRCm39) K418R probably damaging Het
Cic T G 7: 24,971,032 (GRCm39) D254E probably damaging Het
Ckap4 T C 10: 84,363,431 (GRCm39) E544G probably damaging Het
Crnkl1 C T 2: 145,763,739 (GRCm39) A500T probably damaging Het
Daam1 A T 12: 71,990,916 (GRCm39) I177L unknown Het
Ercc5 A G 1: 44,219,784 (GRCm39) T1019A probably damaging Het
F13b T A 1: 139,435,374 (GRCm39) V173E probably damaging Het
Fam20a A C 11: 109,568,143 (GRCm39) F316V probably damaging Het
Flrt2 T C 12: 95,746,112 (GRCm39) V150A probably damaging Het
Fnta A C 8: 26,489,599 (GRCm39) probably null Het
Ghsr A G 3: 27,426,025 (GRCm39) D27G probably benign Het
Gtpbp1 A G 15: 79,592,086 (GRCm39) N96D probably damaging Het
H1f7 A T 15: 98,154,454 (GRCm39) W232R unknown Het
Ibtk A T 9: 85,606,198 (GRCm39) I443N probably damaging Het
Ifi207 T C 1: 173,552,513 (GRCm39) H968R probably damaging Het
Ifit2 A G 19: 34,550,586 (GRCm39) D42G probably null Het
Il17rc A T 6: 113,455,950 (GRCm39) D265V probably damaging Het
Itfg2 T C 6: 128,401,691 (GRCm39) D29G probably damaging Het
Itprid1 A G 6: 55,952,649 (GRCm39) H864R probably damaging Het
Lrrc1 A G 9: 77,349,547 (GRCm39) F295L probably benign Het
Mrps28 T A 3: 8,965,184 (GRCm39) H85L possibly damaging Het
Mtpn T A 6: 35,499,693 (GRCm39) K37M possibly damaging Het
Mug1 C T 6: 121,859,588 (GRCm39) H1196Y probably benign Het
Mup4 T C 4: 59,960,084 (GRCm39) H60R possibly damaging Het
Mybl2 T C 2: 162,914,628 (GRCm39) S249P probably benign Het
Naip6 A G 13: 100,436,748 (GRCm39) Y592H possibly damaging Het
Nrp1 A G 8: 129,229,279 (GRCm39) N919S probably benign Het
Nudt9 C T 5: 104,212,904 (GRCm39) Q326* probably null Het
Or5w13 A T 2: 87,523,720 (GRCm39) C169S probably damaging Het
Or6c76b A G 10: 129,693,100 (GRCm39) T238A probably damaging Het
Or7g17 T A 9: 18,768,407 (GRCm39) M162K probably benign Het
Or9k7 T A 10: 130,046,592 (GRCm39) I136F probably benign Het
Pcsk4 T C 10: 80,161,815 (GRCm39) E142G probably damaging Het
Pde3a C A 6: 141,405,560 (GRCm39) P471T probably benign Het
Pign A T 1: 105,512,727 (GRCm39) V652E possibly damaging Het
Prkcb T A 7: 122,181,672 (GRCm39) M420K probably damaging Het
Prr14 T A 7: 127,073,160 (GRCm39) probably null Het
Rchy1 T A 5: 92,105,741 (GRCm39) Q69L probably damaging Het
Sec23ip T G 7: 128,367,862 (GRCm39) S625A probably benign Het
Smpdl3b A G 4: 132,473,925 (GRCm39) S47P probably damaging Het
Speer4a3 T A 5: 26,156,623 (GRCm39) I119F possibly damaging Het
Stil G A 4: 114,881,161 (GRCm39) M568I probably benign Het
Syt3 T A 7: 44,045,434 (GRCm39) V558E probably damaging Het
Szt2 A G 4: 118,231,164 (GRCm39) V2533A unknown Het
Tenm4 A G 7: 96,353,360 (GRCm39) Y384C probably damaging Het
Tfam T C 10: 71,071,380 (GRCm39) E94G probably damaging Het
Tmbim7 A G 5: 3,714,304 (GRCm39) T14A probably damaging Het
Tmtc2 A T 10: 105,409,566 (GRCm39) Y15* probably null Het
Uhrf1 C T 17: 56,625,035 (GRCm39) A526V probably damaging Het
Vmn2r67 T C 7: 84,805,046 (GRCm39) D22G probably benign Het
Vmn2r96 A G 17: 18,817,660 (GRCm39) I412M possibly damaging Het
Wdr17 A T 8: 55,123,363 (GRCm39) I479K probably damaging Het
Wt1 T C 2: 104,997,176 (GRCm39) V371A probably damaging Het
Zfp536 G T 7: 37,178,735 (GRCm39) S226Y probably damaging Het
Zfp827 T C 8: 79,803,108 (GRCm39) V560A probably benign Het
Other mutations in Cyp2c38
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00508:Cyp2c38 APN 19 39,449,169 (GRCm39) nonsense probably null
IGL01109:Cyp2c38 APN 19 39,451,329 (GRCm39) critical splice donor site probably null
IGL01521:Cyp2c38 APN 19 39,449,114 (GRCm39) missense probably damaging 0.99
IGL02036:Cyp2c38 APN 19 39,448,760 (GRCm39) missense probably null 0.97
IGL02187:Cyp2c38 APN 19 39,424,649 (GRCm39) missense probably benign 0.14
IGL02954:Cyp2c38 APN 19 39,379,520 (GRCm39) missense probably damaging 0.99
R0479:Cyp2c38 UTSW 19 39,451,449 (GRCm39) missense probably damaging 0.99
R0684:Cyp2c38 UTSW 19 39,379,500 (GRCm39) missense probably damaging 0.99
R0919:Cyp2c38 UTSW 19 39,393,113 (GRCm39) missense probably benign 0.07
R1462:Cyp2c38 UTSW 19 39,380,632 (GRCm39) missense probably damaging 0.96
R1642:Cyp2c38 UTSW 19 39,390,153 (GRCm39) missense probably damaging 1.00
R1715:Cyp2c38 UTSW 19 39,393,239 (GRCm39) missense probably benign 0.25
R1900:Cyp2c38 UTSW 19 39,426,756 (GRCm39) missense probably benign 0.40
R1954:Cyp2c38 UTSW 19 39,393,131 (GRCm39) missense probably damaging 0.99
R1955:Cyp2c38 UTSW 19 39,393,131 (GRCm39) missense probably damaging 0.99
R2860:Cyp2c38 UTSW 19 39,449,138 (GRCm39) missense probably benign 0.01
R2861:Cyp2c38 UTSW 19 39,449,138 (GRCm39) missense probably benign 0.01
R2862:Cyp2c38 UTSW 19 39,449,138 (GRCm39) missense probably benign 0.01
R3084:Cyp2c38 UTSW 19 39,390,145 (GRCm39) missense probably benign 0.00
R3727:Cyp2c38 UTSW 19 39,380,739 (GRCm39) splice site probably benign
R4648:Cyp2c38 UTSW 19 39,449,132 (GRCm39) missense probably benign 0.05
R5119:Cyp2c38 UTSW 19 39,449,065 (GRCm39) missense probably damaging 1.00
R5636:Cyp2c38 UTSW 19 39,426,750 (GRCm39) nonsense probably null
R5651:Cyp2c38 UTSW 19 39,449,156 (GRCm39) missense probably damaging 0.99
R6263:Cyp2c38 UTSW 19 39,380,659 (GRCm39) missense probably damaging 1.00
R6384:Cyp2c38 UTSW 19 39,380,737 (GRCm39) splice site probably null
R6853:Cyp2c38 UTSW 19 39,426,748 (GRCm39) missense probably benign 0.02
R6915:Cyp2c38 UTSW 19 39,424,512 (GRCm39) missense probably damaging 0.99
R7201:Cyp2c38 UTSW 19 39,390,220 (GRCm39) missense probably damaging 1.00
R7570:Cyp2c38 UTSW 19 39,393,187 (GRCm39) missense possibly damaging 0.76
R7625:Cyp2c38 UTSW 19 39,451,368 (GRCm39) missense possibly damaging 0.78
R7666:Cyp2c38 UTSW 19 39,426,686 (GRCm39) missense possibly damaging 0.52
R8681:Cyp2c38 UTSW 19 39,390,135 (GRCm39) missense possibly damaging 0.70
Predicted Primers
Posted On 2014-03-14