Incidental Mutation 'R1715:Cyp2c38'
ID 190971
Institutional Source Beutler Lab
Gene Symbol Cyp2c38
Ensembl Gene ENSMUSG00000032808
Gene Name cytochrome P450, family 2, subfamily c, polypeptide 38
Synonyms
MMRRC Submission 039748-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # R1715 (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 39393239 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 276 (H276R)
Ref Sequence ENSEMBL: ENSMUSP00000044722 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035488]
AlphaFold P56655
Predicted Effect probably benign
Transcript: ENSMUST00000035488
AA Change: H276R

PolyPhen 2 Score 0.248 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000044722
Gene: ENSMUSG00000032808
AA Change: H276R

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:p450 30 487 1.5e-161 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a G A 11: 109,982,406 (GRCm39) T12M probably damaging Het
Alms1 T A 6: 85,606,034 (GRCm39) Y2561* probably null Het
Atp10a G A 7: 58,436,253 (GRCm39) V348I probably damaging Het
Best2 T C 8: 85,737,852 (GRCm39) Y181C probably benign Het
Btaf1 T A 19: 36,946,521 (GRCm39) D442E probably damaging Het
Carmil3 T G 14: 55,741,989 (GRCm39) V1153G probably benign Het
Cc2d2a A G 5: 43,876,003 (GRCm39) I993M probably damaging Het
Ccng1 G A 11: 40,642,941 (GRCm39) P169S probably benign Het
Cip2a C T 16: 48,826,082 (GRCm39) T383I probably benign Het
Cmtr2 T C 8: 110,949,430 (GRCm39) L580P probably damaging Het
Col22a1 T C 15: 71,878,830 (GRCm39) E109G possibly damaging Het
Cplane1 T A 15: 8,256,384 (GRCm39) probably null Het
Crispld2 G T 8: 120,750,388 (GRCm39) W264L possibly damaging Het
Dag1 A T 9: 108,085,914 (GRCm39) V409E possibly damaging Het
Efcab15 T C 11: 103,090,650 (GRCm39) probably null Het
Emc8 T C 8: 121,385,294 (GRCm39) N146S probably benign Het
Glt8d1 T C 14: 30,733,478 (GRCm39) V321A possibly damaging Het
Gm5174 C T 10: 86,492,776 (GRCm39) noncoding transcript Het
Hdac10 G T 15: 89,010,912 (GRCm39) probably null Het
Hectd4 A G 5: 121,482,881 (GRCm39) D3144G possibly damaging Het
Ifna11 C T 4: 88,738,473 (GRCm39) S93L probably damaging Het
Il16 T C 7: 83,297,936 (GRCm39) N431S probably benign Het
Irf8 A T 8: 121,481,127 (GRCm39) E237V probably damaging Het
Lrp1b A G 2: 41,075,993 (GRCm39) Y1769H probably damaging Het
Lrrc9 A G 12: 72,524,073 (GRCm39) N761D probably damaging Het
Mbtps1 T C 8: 120,269,469 (GRCm39) Y207C probably benign Het
Myo9a A G 9: 59,739,583 (GRCm39) E765G probably damaging Het
Nlrp3 A G 11: 59,434,177 (GRCm39) D80G probably damaging Het
Or12k8 G A 2: 36,975,188 (GRCm39) P191S probably damaging Het
Or2ag15 G C 7: 106,340,755 (GRCm39) P129A probably damaging Het
Or7g18 A T 9: 18,787,090 (GRCm39) I156F probably benign Het
Pcyt2 T A 11: 120,506,677 (GRCm39) probably null Het
Plxnd1 T C 6: 115,945,642 (GRCm39) T944A probably benign Het
Prss3b A G 6: 41,009,870 (GRCm39) probably null Het
Psd4 A T 2: 24,295,344 (GRCm39) I833F probably damaging Het
Psmd7 A G 8: 108,307,817 (GRCm39) I222T probably benign Het
Rap2b A G 3: 61,272,611 (GRCm39) E45G probably damaging Het
Rbm22 T C 18: 60,693,916 (GRCm39) S7P possibly damaging Het
Rbpms2 ACTGCTGCTGCTGCTGC ACTGCTGCTGCTGCTGCTGC 9: 65,558,948 (GRCm39) probably benign Het
Rfx4 A G 10: 84,680,144 (GRCm39) N107S probably damaging Het
Ripk2 T A 4: 16,155,192 (GRCm39) probably null Het
Rpgrip1 T A 14: 52,378,148 (GRCm39) C499S possibly damaging Het
Scarf1 T C 11: 75,414,870 (GRCm39) S515P probably damaging Het
Sgip1 T C 4: 102,772,256 (GRCm39) V215A probably benign Het
Sis T C 3: 72,796,343 (GRCm39) I1813V possibly damaging Het
Slc17a3 A T 13: 24,040,724 (GRCm39) T317S probably benign Het
Slc35e1 T C 8: 73,237,821 (GRCm39) N340S probably benign Het
Smg6 A G 11: 74,820,256 (GRCm39) I176V probably benign Het
Smim17 T C 7: 6,432,325 (GRCm39) L89S probably damaging Het
Synm T C 7: 67,386,051 (GRCm39) N95S probably damaging Het
Tdrd9 A G 12: 112,002,873 (GRCm39) K841E possibly damaging Het
Tep1 G T 14: 51,092,024 (GRCm39) F570L possibly damaging Het
Tgm3 G A 2: 129,868,734 (GRCm39) probably null Het
Tra2b T C 16: 22,071,496 (GRCm39) Y128C possibly damaging Het
Vmn2r17 T C 5: 109,576,110 (GRCm39) V327A probably benign Het
Wdr20rt A T 12: 65,274,088 (GRCm39) D344V probably damaging Het
Zfp940 A G 7: 29,544,363 (GRCm39) C515R probably damaging 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
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
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 PCR Primer
(F):5'- TCCAGCAACTTAGAGGACCACTGT -3'
(R):5'- ttctgggctaataAGGGGCAAAGAATC -3'

Sequencing Primer
(F):5'- CACTGTGGTTTACCAACTATGC -3'
(R):5'- GGACTCAAAGTCTATTCAACTTGGTG -3'
Posted On 2014-05-14