Incidental Mutation 'IGL02723:Cyp2j7'
ID 305051
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp2j7
Ensembl Gene ENSMUSG00000081362
Gene Name cytochrome P450, family 2, subfamily j, polypeptide 7
Synonyms OTTMUSG00000007941, Cyp2j7-ps
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02723
Quality Score
Status
Chromosome 4
Chromosomal Location 96083434-96124896 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 96118366 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 76 (K76E)
Ref Sequence ENSEMBL: ENSMUSP00000134331 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000162514]
AlphaFold A0A140T8U1
Predicted Effect probably benign
Transcript: ENSMUST00000162514
AA Change: K76E

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000134331
Gene: ENSMUSG00000081362
AA Change: K76E

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
Pfam:p450 44 499 3.7e-130 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Capn9 A T 8: 125,335,922 (GRCm39) probably benign Het
Cchcr1 A C 17: 35,841,699 (GRCm39) K761Q probably benign Het
Cfap20dc T C 14: 8,516,507 (GRCm38) N347S probably benign Het
Csk G T 9: 57,538,672 (GRCm39) probably benign Het
Dpep1 G A 8: 123,920,888 (GRCm39) A23T possibly damaging Het
Dpp8 T A 9: 64,949,549 (GRCm39) M98K possibly damaging Het
Dspp C A 5: 104,323,041 (GRCm39) N61K probably benign Het
Eno2 T C 6: 124,738,626 (GRCm39) Y364C probably damaging Het
Gfra1 A G 19: 58,441,683 (GRCm39) S83P probably benign Het
Gramd1b T C 9: 40,218,127 (GRCm39) E563G probably damaging Het
Kcns2 G T 15: 34,838,961 (GRCm39) W108L probably damaging Het
Mroh4 T C 15: 74,480,086 (GRCm39) probably benign Het
Obscn A T 11: 59,015,446 (GRCm39) S1009T probably benign Het
Or2y11 A G 11: 49,443,506 (GRCm39) R311G probably benign Het
Or5b119 A G 19: 13,456,699 (GRCm39) Y288H probably damaging Het
Or7g32 T C 9: 19,388,805 (GRCm39) H244R probably damaging Het
Or8b41 A G 9: 38,054,707 (GRCm39) K92R probably benign Het
Plcb2 G A 2: 118,547,500 (GRCm39) probably benign Het
Rpl13a-ps1 T A 19: 50,019,111 (GRCm39) I22F possibly damaging Het
Skil A G 3: 31,171,673 (GRCm39) E599G probably damaging Het
Snx19 A G 9: 30,343,556 (GRCm39) N572S possibly damaging Het
Spata31 T C 13: 65,068,463 (GRCm39) S204P probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tenm3 A T 8: 48,729,938 (GRCm39) V1356E probably benign Het
Trpc3 T A 3: 36,704,377 (GRCm39) I527F probably benign Het
Vmn2r69 A G 7: 85,059,416 (GRCm39) W498R probably damaging Het
Vwde T A 6: 13,205,759 (GRCm39) I263L probably damaging Het
Vwf G T 6: 125,619,893 (GRCm39) V1524L possibly damaging Het
Wdr55 A G 18: 36,896,435 (GRCm39) E375G probably benign 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
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
R9254:Cyp2j7 UTSW 4 96,105,740 (GRCm39) nonsense 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
Posted On 2015-04-16