Incidental Mutation 'R9254:Cyp2j7'
ID 701709
Institutional Source Beutler Lab
Gene Symbol Cyp2j7
Ensembl Gene ENSMUSG00000081362
Gene Name cytochrome P450, family 2, subfamily j, polypeptide 7
Synonyms OTTMUSG00000007941, Cyp2j7-ps
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R9254 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 96083434-96124896 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 96105740 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 257 (K257*)
Ref Sequence ENSEMBL: ENSMUSP00000134331 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000162514]
AlphaFold A0A140T8U1
Predicted Effect probably null
Transcript: ENSMUST00000162514
AA Change: K257*
SMART Domains Protein: ENSMUSP00000134331
Gene: ENSMUSG00000081362
AA Change: K257*

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
Pfam:p450 44 499 3.7e-130 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aak1 A G 6: 86,914,049 (GRCm39) I173V possibly damaging Het
Abca14 G T 7: 119,807,202 (GRCm39) E83* probably null Het
Abcc5 T C 16: 20,152,437 (GRCm39) T1370A probably damaging Het
Abtb2 A G 2: 103,541,580 (GRCm39) T828A probably benign Het
Agap1 T A 1: 89,653,741 (GRCm39) V370D probably damaging Het
Ankhd1 T C 18: 36,777,680 (GRCm39) V1621A probably benign Het
Atp2a2 T C 5: 122,611,315 (GRCm39) I168V probably benign Het
Atxn2 G A 5: 121,885,509 (GRCm39) V239I probably damaging Het
B230219D22Rik C A 13: 55,847,283 (GRCm39) A132E probably damaging Het
Bod1l T C 5: 41,979,223 (GRCm39) E697G probably damaging Het
Ccdc162 T G 10: 41,488,944 (GRCm39) probably null Het
Chd7 A G 4: 8,752,210 (GRCm39) S236G unknown Het
Csmd2 A G 4: 128,091,112 (GRCm39) E217G Het
D630003M21Rik C T 2: 158,042,883 (GRCm39) A886T probably damaging Het
D630044L22Rik A G 17: 26,180,856 (GRCm39) H102R possibly damaging Het
Dact3 G A 7: 16,620,013 (GRCm39) V503I unknown Het
Dcn G T 10: 97,343,643 (GRCm39) R201L probably damaging Het
Dmxl1 T C 18: 50,024,567 (GRCm39) V1747A possibly damaging Het
Dnajc14 T A 10: 128,652,743 (GRCm39) probably null Het
Dner A G 1: 84,673,193 (GRCm39) V86A probably benign Het
Dspp A T 5: 104,322,760 (GRCm39) probably null Het
Gphn T C 12: 78,674,036 (GRCm39) probably null Het
Gpr158 A G 2: 21,373,042 (GRCm39) probably benign Het
Grip1 G T 10: 119,780,961 (GRCm39) L203F probably damaging Het
Hgfac T C 5: 35,202,133 (GRCm39) W345R probably damaging Het
Hoga1 T C 19: 42,051,697 (GRCm39) L250P probably damaging Het
Ighv1-24 T C 12: 114,736,663 (GRCm39) Y79C possibly damaging Het
Katnip T C 7: 125,469,848 (GRCm39) L1439P probably damaging Het
Kif21a C T 15: 90,854,030 (GRCm39) R779Q probably damaging Het
Klkb1 T C 8: 45,742,067 (GRCm39) T71A probably benign Het
Lama2 A G 10: 27,298,685 (GRCm39) V137A probably damaging Het
Lrp2 T C 2: 69,333,891 (GRCm39) D1450G probably benign Het
Lrrc8c T A 5: 105,756,356 (GRCm39) Y710* probably null Het
Mixl1 A G 1: 180,522,258 (GRCm39) S208P probably benign Het
Mroh1 A G 15: 76,292,215 (GRCm39) H229R probably benign Het
Muc16 T A 9: 18,557,467 (GRCm39) Q2942L unknown Het
Nicn1 C T 9: 108,171,708 (GRCm39) R163C possibly damaging Het
Nos1 G C 5: 118,017,402 (GRCm39) R255P probably benign Het
Nup85 T C 11: 115,469,424 (GRCm39) I322T probably benign Het
Odad1 A G 7: 45,597,116 (GRCm39) T456A probably benign Het
Odad2 T C 18: 7,265,089 (GRCm39) D426G possibly damaging Het
Or10n7-ps1 A G 9: 39,598,114 (GRCm39) L42P probably damaging Het
Or5w15 T A 2: 87,568,372 (GRCm39) M99L probably benign Het
Or7e169 T A 9: 19,757,212 (GRCm39) K234N possibly damaging Het
Or8b4 C T 9: 37,830,447 (GRCm39) L165F probably damaging Het
Or9k2b A G 10: 130,016,605 (GRCm39) M48T possibly damaging Het
Pcyt1a G A 16: 32,288,894 (GRCm39) R245Q probably benign Het
Pi15 T C 1: 17,695,180 (GRCm39) Y266H probably benign Het
Plxna2 C T 1: 194,492,474 (GRCm39) T1777I probably damaging Het
Ppp3cb T C 14: 20,581,874 (GRCm39) D47G probably benign Het
Pram1 T C 17: 33,860,441 (GRCm39) V336A probably damaging Het
Prl T A 13: 27,243,503 (GRCm39) I58N probably damaging Het
Qrich2 T C 11: 116,348,934 (GRCm39) D630G unknown Het
Ralgapa1 G C 12: 55,769,583 (GRCm39) P803A probably damaging Het
Rin1 A G 19: 5,103,249 (GRCm39) K513E probably damaging Het
Rtcb A T 10: 85,779,071 (GRCm39) probably null Het
Ryr2 C T 13: 11,898,002 (GRCm39) C131Y probably damaging Het
Sspo G T 6: 48,464,928 (GRCm39) V3954L probably damaging Het
Taf4b C T 18: 14,946,431 (GRCm39) T418M probably damaging Het
Taf6 A G 5: 138,181,952 (GRCm39) I92T possibly damaging Het
Tfg A T 16: 56,526,050 (GRCm39) D64E probably damaging Het
Tkfc T A 19: 10,574,712 (GRCm39) E176V probably damaging Het
Tmco1 C T 1: 167,136,132 (GRCm39) probably benign Het
Tmem200a A T 10: 25,869,654 (GRCm39) L205Q probably damaging Het
Trav13n-3 T G 14: 53,574,853 (GRCm39) L32V probably damaging Het
Tsen2 T A 6: 115,553,864 (GRCm39) M414K probably damaging Het
Tut7 T C 13: 59,936,288 (GRCm39) Y1271C possibly damaging Het
Txlna A T 4: 129,530,900 (GRCm39) Y196N probably damaging Het
Usp44 T A 10: 93,688,635 (GRCm39) I562K possibly damaging Het
Vmn1r24 T A 6: 57,932,736 (GRCm39) I261F probably benign Het
Vmn2r106 T C 17: 20,496,066 (GRCm39) T553A probably damaging Het
Vmn2r65 A G 7: 84,596,650 (GRCm39) V135A probably damaging Het
Other mutations in Cyp2j7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00426:Cyp2j7 APN 4 96,115,750 (GRCm39) splice site probably null
IGL00426:Cyp2j7 APN 4 96,115,749 (GRCm39) splice site probably benign
IGL01505:Cyp2j7 APN 4 96,115,917 (GRCm39) critical splice acceptor site probably null
IGL02100:Cyp2j7 APN 4 96,124,793 (GRCm39) missense probably damaging 0.99
IGL02183:Cyp2j7 APN 4 96,118,384 (GRCm39) splice site probably benign
IGL02596:Cyp2j7 APN 4 96,103,659 (GRCm39) missense possibly damaging 0.56
IGL02661:Cyp2j7 APN 4 96,124,887 (GRCm39) missense probably benign
IGL02723:Cyp2j7 APN 4 96,118,366 (GRCm39) missense probably benign 0.33
IGL03053:Cyp2j7 APN 4 96,118,274 (GRCm39) missense probably benign 0.00
IGL03159:Cyp2j7 APN 4 96,115,749 (GRCm39) splice site probably benign
IGL03168:Cyp2j7 APN 4 96,118,274 (GRCm39) missense probably benign 0.00
IGL03174:Cyp2j7 APN 4 96,083,607 (GRCm39) nonsense probably null
PIT4449001:Cyp2j7 UTSW 4 96,103,575 (GRCm39) missense probably damaging 0.96
R0016:Cyp2j7 UTSW 4 96,090,384 (GRCm39) missense probably damaging 0.99
R0016:Cyp2j7 UTSW 4 96,090,384 (GRCm39) missense probably damaging 0.99
R0392:Cyp2j7 UTSW 4 96,087,671 (GRCm39) missense probably damaging 1.00
R1447:Cyp2j7 UTSW 4 96,083,530 (GRCm39) missense possibly damaging 0.90
R1778:Cyp2j7 UTSW 4 96,087,627 (GRCm39) missense probably damaging 1.00
R1876:Cyp2j7 UTSW 4 96,105,656 (GRCm39) missense probably benign 0.01
R4105:Cyp2j7 UTSW 4 96,087,687 (GRCm39) missense possibly damaging 0.84
R4106:Cyp2j7 UTSW 4 96,087,687 (GRCm39) missense possibly damaging 0.84
R4107:Cyp2j7 UTSW 4 96,087,687 (GRCm39) missense possibly damaging 0.84
R4108:Cyp2j7 UTSW 4 96,087,687 (GRCm39) missense possibly damaging 0.84
R4438:Cyp2j7 UTSW 4 96,105,646 (GRCm39) missense probably benign 0.01
R4660:Cyp2j7 UTSW 4 96,083,579 (GRCm39) missense probably benign 0.29
R6193:Cyp2j7 UTSW 4 96,083,440 (GRCm39) missense probably damaging 1.00
R6380:Cyp2j7 UTSW 4 96,118,211 (GRCm39) critical splice donor site probably null
R6427:Cyp2j7 UTSW 4 96,115,904 (GRCm39) missense probably damaging 0.96
R6624:Cyp2j7 UTSW 4 96,115,855 (GRCm39) missense probably damaging 0.99
R7196:Cyp2j7 UTSW 4 96,103,651 (GRCm39) missense probably benign 0.03
R7417:Cyp2j7 UTSW 4 96,090,225 (GRCm39) critical splice donor site probably null
R7780:Cyp2j7 UTSW 4 96,118,256 (GRCm39) missense probably benign 0.00
R8062:Cyp2j7 UTSW 4 96,103,587 (GRCm39) missense probably null 1.00
R8097:Cyp2j7 UTSW 4 96,103,647 (GRCm39) missense possibly damaging 0.95
R8201:Cyp2j7 UTSW 4 96,083,564 (GRCm39) missense probably damaging 1.00
R8279:Cyp2j7 UTSW 4 96,116,796 (GRCm39) critical splice donor site probably null
R9328:Cyp2j7 UTSW 4 96,115,869 (GRCm39) missense probably damaging 1.00
R9377:Cyp2j7 UTSW 4 96,124,786 (GRCm39) missense probably benign 0.01
R9489:Cyp2j7 UTSW 4 96,103,591 (GRCm39) missense probably damaging 1.00
R9499:Cyp2j7 UTSW 4 96,115,840 (GRCm39) missense probably damaging 1.00
R9552:Cyp2j7 UTSW 4 96,115,840 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GACAGCATGATGTAAGGTCCACTG -3'
(R):5'- GAGCTGAAGCACATGATAACC -3'

Sequencing Primer
(F):5'- GATGTAAGGTCCACTGAAAACTTG -3'
(R):5'- CATGATAACCTGAAACCAAGATGG -3'
Posted On 2022-03-25