Incidental Mutation 'R4078:Cyp2b23'
ID 316688
Institutional Source Beutler Lab
Gene Symbol Cyp2b23
Ensembl Gene ENSMUSG00000040650
Gene Name cytochrome P450, family 2, subfamily b, polypeptide 23
Synonyms EG243881
MMRRC Submission 041623-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # R4078 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 26364652-26385862 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 26372517 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Valine at position 366 (G366V)
Ref Sequence ENSEMBL: ENSMUSP00000076578 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077356]
AlphaFold E9Q593
Predicted Effect probably damaging
Transcript: ENSMUST00000077356
AA Change: G366V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000076578
Gene: ENSMUSG00000040650
AA Change: G366V

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:p450 31 488 2.9e-148 PFAM
Meta Mutation Damage Score 0.7560 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 96% (70/73)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931429L15Rik A T 9: 46,215,359 (GRCm39) L367* probably null Het
Agfg1 T A 1: 82,860,008 (GRCm39) S312T possibly damaging Het
Akap8 C T 17: 32,531,272 (GRCm39) R380Q probably damaging Het
Ambp T A 4: 63,068,680 (GRCm39) K112N probably damaging Het
Arl5c A T 11: 97,884,327 (GRCm39) I88N probably damaging Het
Asah1 A G 8: 41,807,119 (GRCm39) S102P probably damaging Het
Atp10b T C 11: 43,044,110 (GRCm39) V112A probably benign Het
C3 C T 17: 57,512,303 (GRCm39) D1542N possibly damaging Het
Cabs1 G A 5: 88,128,161 (GRCm39) E271K probably damaging Het
Car8 T C 4: 8,169,731 (GRCm39) K259R possibly damaging Het
Ccdc18 C T 5: 108,306,394 (GRCm39) Q270* probably null Het
Cdh4 A G 2: 179,530,966 (GRCm39) E616G possibly damaging Het
Cdk11b C T 4: 155,724,204 (GRCm39) probably benign Het
Cfap74 A G 4: 155,540,128 (GRCm39) D975G probably damaging Het
Col27a1 G T 4: 63,142,669 (GRCm39) R119L probably damaging Het
Col7a1 A G 9: 108,790,059 (GRCm39) N918S unknown Het
Colec11 T C 12: 28,645,246 (GRCm39) N142D possibly damaging Het
Cox7a2 G A 9: 79,665,852 (GRCm39) Q10* probably null Het
Eif1ad3 A G 12: 87,843,401 (GRCm39) K16R unknown Het
Emsy G A 7: 98,239,932 (GRCm39) P1108S probably damaging Het
Etl4 A T 2: 20,812,772 (GRCm39) R1442S probably damaging Het
Fam151a G A 4: 106,604,954 (GRCm39) G439S probably benign Het
Fat1 C T 8: 45,442,159 (GRCm39) P1154S probably damaging Het
Fat4 G A 3: 39,034,169 (GRCm39) S2607N probably damaging Het
Fzd7 T A 1: 59,522,948 (GRCm39) M277K possibly damaging Het
Fzd9 A G 5: 135,278,490 (GRCm39) V465A probably benign Het
Gm38706 G T 6: 130,460,700 (GRCm39) noncoding transcript Het
Gm9758 T A 5: 14,961,536 (GRCm39) probably null Het
Gpr3 T C 4: 132,938,226 (GRCm39) T149A probably damaging Het
Heatr9 C A 11: 83,403,254 (GRCm39) K428N probably benign Het
Hgs T A 11: 120,373,874 (GRCm39) S723T probably benign Het
Hsh2d G A 8: 72,954,304 (GRCm39) D229N probably benign Het
Kcnn3 A G 3: 89,568,495 (GRCm39) K591R possibly damaging Het
Khdrbs2 T C 1: 32,558,895 (GRCm39) probably benign Het
Lpp G A 16: 24,500,611 (GRCm39) R141H probably damaging Het
Lrpap1 A G 5: 35,253,381 (GRCm39) I261T possibly damaging Het
Macf1 T A 4: 123,365,884 (GRCm39) Q2959L probably benign Het
Mipep T A 14: 61,083,926 (GRCm39) Y606N probably damaging Het
Mroh5 C A 15: 73,657,889 (GRCm39) C547F possibly damaging Het
Nek3 A T 8: 22,622,153 (GRCm39) W363R probably damaging Het
Nphs1 T A 7: 30,166,945 (GRCm39) Y717* probably null Het
Obscn A G 11: 58,929,189 (GRCm39) V6145A probably benign Het
Optc T C 1: 133,826,087 (GRCm39) H270R probably damaging Het
Or1l4 T A 2: 37,092,024 (GRCm39) I257N possibly damaging Het
Or2l5 T A 16: 19,333,982 (GRCm39) M135L possibly damaging Het
Or5p80 T A 7: 108,230,114 (GRCm39) M305K probably benign Het
Or9r7 G A 10: 129,962,587 (GRCm39) T113I probably damaging Het
Pik3c2g A G 6: 139,612,608 (GRCm39) probably benign Het
Pms1 A T 1: 53,306,948 (GRCm39) probably null Het
Pramel51 T A 12: 88,142,683 (GRCm39) I312F probably benign Het
Prkg1 T C 19: 31,562,978 (GRCm39) Y156C probably damaging Het
Prol1 A G 5: 88,476,075 (GRCm39) N155S unknown Het
Rapgefl1 A G 11: 98,740,803 (GRCm39) T552A probably benign Het
Slc22a28 T A 19: 8,078,777 (GRCm39) H304L probably benign Het
Stox1 C T 10: 62,501,810 (GRCm39) C250Y probably benign Het
Sult2a3 A G 7: 13,855,662 (GRCm39) W65R possibly damaging Het
Syce1 C A 7: 140,359,809 (GRCm39) L83F probably damaging Het
Syne2 C A 12: 76,082,398 (GRCm39) T4857K probably damaging Het
Tcp1 T C 17: 13,136,970 (GRCm39) L64S probably benign Het
Thap11 G T 8: 106,582,548 (GRCm39) E186* probably null Het
Tmem67 A G 4: 12,040,633 (GRCm39) probably null Het
Trappc10 T C 10: 78,046,216 (GRCm39) Y458C probably damaging Het
Ufd1 A G 16: 18,644,528 (GRCm39) Y197C possibly damaging Het
Ung G T 5: 114,268,684 (GRCm39) probably null Het
Usp49 A G 17: 47,985,674 (GRCm39) T245A probably damaging Het
Washc1 A T 17: 66,424,156 (GRCm39) E289D probably benign Het
Zc3h7a A T 16: 10,969,011 (GRCm39) V450E probably benign Het
Zcchc17 T G 4: 130,223,418 (GRCm39) I123L possibly damaging Het
Zfp955a A G 17: 33,460,675 (GRCm39) Y486H probably benign Het
Other mutations in Cyp2b23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01716:Cyp2b23 APN 7 26,378,915 (GRCm39) missense probably damaging 0.98
IGL01879:Cyp2b23 APN 7 26,372,279 (GRCm39) missense probably benign 0.04
IGL02207:Cyp2b23 APN 7 26,381,180 (GRCm39) missense probably damaging 1.00
IGL03047:Cyp2b23 APN 7 26,380,892 (GRCm39) splice site probably benign
R0117:Cyp2b23 UTSW 7 26,372,539 (GRCm39) missense probably benign 0.25
R0265:Cyp2b23 UTSW 7 26,372,304 (GRCm39) splice site probably benign
R1457:Cyp2b23 UTSW 7 26,372,574 (GRCm39) missense probably damaging 1.00
R1605:Cyp2b23 UTSW 7 26,385,843 (GRCm39) missense probably benign 0.02
R1639:Cyp2b23 UTSW 7 26,385,842 (GRCm39) missense possibly damaging 0.77
R1741:Cyp2b23 UTSW 7 26,372,502 (GRCm39) missense possibly damaging 0.94
R2042:Cyp2b23 UTSW 7 26,365,533 (GRCm39) missense probably damaging 1.00
R3911:Cyp2b23 UTSW 7 26,380,842 (GRCm39) missense probably benign 0.02
R4279:Cyp2b23 UTSW 7 26,365,452 (GRCm39) missense possibly damaging 0.89
R4668:Cyp2b23 UTSW 7 26,372,159 (GRCm39) missense probably damaging 1.00
R5419:Cyp2b23 UTSW 7 26,380,848 (GRCm39) nonsense probably null
R5516:Cyp2b23 UTSW 7 26,372,482 (GRCm39) nonsense probably null
R5723:Cyp2b23 UTSW 7 26,380,821 (GRCm39) missense probably benign 0.41
R5873:Cyp2b23 UTSW 7 26,374,431 (GRCm39) missense probably benign 0.02
R6346:Cyp2b23 UTSW 7 26,381,150 (GRCm39) missense probably damaging 0.98
R6977:Cyp2b23 UTSW 7 26,380,745 (GRCm39) missense possibly damaging 0.87
R7131:Cyp2b23 UTSW 7 26,380,838 (GRCm39) missense probably benign 0.25
R7181:Cyp2b23 UTSW 7 26,373,828 (GRCm39) missense probably damaging 1.00
R7715:Cyp2b23 UTSW 7 26,381,120 (GRCm39) missense probably benign
R7877:Cyp2b23 UTSW 7 26,385,851 (GRCm39) missense probably damaging 0.97
R7880:Cyp2b23 UTSW 7 26,372,559 (GRCm39) missense probably damaging 1.00
R8004:Cyp2b23 UTSW 7 26,378,891 (GRCm39) missense probably benign
R8072:Cyp2b23 UTSW 7 26,365,431 (GRCm39) missense probably damaging 1.00
R8083:Cyp2b23 UTSW 7 26,385,828 (GRCm39) missense possibly damaging 0.62
R8968:Cyp2b23 UTSW 7 26,378,963 (GRCm39) missense probably damaging 0.99
R9129:Cyp2b23 UTSW 7 26,381,189 (GRCm39) splice site probably benign
R9437:Cyp2b23 UTSW 7 26,372,199 (GRCm39) missense possibly damaging 0.68
R9794:Cyp2b23 UTSW 7 26,381,121 (GRCm39) missense probably benign 0.14
Z1088:Cyp2b23 UTSW 7 26,380,836 (GRCm39) missense probably benign 0.06
Predicted Primers PCR Primer
(F):5'- AGATGTTCACAAACCCTGACTC -3'
(R):5'- TGCTCTGAACTGTTCCTGGG -3'

Sequencing Primer
(F):5'- GATGTTCACAAACCCTGACTCACATG -3'
(R):5'- ACAGGGTCATTGTGCATCAC -3'
Posted On 2015-05-15