Incidental Mutation 'IGL01816:Cyp2j11'
ID 154398
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp2j11
Ensembl Gene ENSMUSG00000066097
Gene Name cytochrome P450, family 2, subfamily j, polypeptide 11
Synonyms Cyp2j11-ps
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # IGL01816
Quality Score
Status
Chromosome 4
Chromosomal Location 96182745-96236899 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 96183161 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Proline at position 469 (Q469P)
Ref Sequence ENSEMBL: ENSMUSP00000132180 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015368]
AlphaFold Q3UNV2
Predicted Effect probably damaging
Transcript: ENSMUST00000015368
AA Change: Q469P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000132180
Gene: ENSMUSG00000066097
AA Change: Q469P

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
Pfam:p450 44 500 4.3e-133 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 T A 13: 81,677,168 (GRCm39) T1888S probably benign Het
Asxl3 T C 18: 22,655,545 (GRCm39) V1185A probably benign Het
Bmp8a G A 4: 123,210,190 (GRCm39) R299C probably damaging Het
Cactin T C 10: 81,161,699 (GRCm39) Y744H possibly damaging Het
Ccr2 A T 9: 123,906,235 (GRCm39) I172L probably benign Het
Dync1i1 T C 6: 5,767,146 (GRCm39) probably null Het
Epb41 A G 4: 131,731,006 (GRCm39) S192P probably benign Het
Gpd2 T A 2: 57,254,078 (GRCm39) Y601* probably null Het
Ift140 G A 17: 25,305,999 (GRCm39) probably null Het
Obscn A G 11: 58,886,605 (GRCm39) probably benign Het
Or10j27 A G 1: 172,957,840 (GRCm39) probably benign Het
Pcdhb13 A C 18: 37,576,028 (GRCm39) R135S probably benign Het
Phtf2 A T 5: 21,008,274 (GRCm39) W136R probably damaging Het
Prpf40b G A 15: 99,213,099 (GRCm39) A662T probably damaging Het
Retsat A G 6: 72,578,588 (GRCm39) N100S probably benign Het
Saxo1 T A 4: 86,363,851 (GRCm39) M211L probably benign Het
Slc5a9 A G 4: 111,755,811 (GRCm39) L29P probably damaging Het
St14 A G 9: 31,019,563 (GRCm39) V86A possibly damaging Het
Tfap4 T C 16: 4,369,956 (GRCm39) N13S probably damaging Het
Other mutations in Cyp2j11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01101:Cyp2j11 APN 4 96,227,332 (GRCm39) missense probably benign
IGL02406:Cyp2j11 APN 4 96,236,776 (GRCm39) missense possibly damaging 0.56
E7848:Cyp2j11 UTSW 4 96,207,602 (GRCm39) missense probably benign 0.09
R0020:Cyp2j11 UTSW 4 96,195,641 (GRCm39) missense probably benign 0.19
R0020:Cyp2j11 UTSW 4 96,195,641 (GRCm39) missense probably benign 0.19
R1298:Cyp2j11 UTSW 4 96,195,497 (GRCm39) critical splice donor site probably null
R1411:Cyp2j11 UTSW 4 96,233,453 (GRCm39) missense probably benign 0.03
R1428:Cyp2j11 UTSW 4 96,183,117 (GRCm39) missense probably benign 0.01
R1740:Cyp2j11 UTSW 4 96,207,613 (GRCm39) missense probably benign 0.00
R1818:Cyp2j11 UTSW 4 96,185,976 (GRCm39) missense probably damaging 0.97
R1819:Cyp2j11 UTSW 4 96,185,976 (GRCm39) missense probably damaging 0.97
R1917:Cyp2j11 UTSW 4 96,228,211 (GRCm39) missense probably damaging 1.00
R2084:Cyp2j11 UTSW 4 96,227,438 (GRCm39) missense probably damaging 1.00
R2146:Cyp2j11 UTSW 4 96,204,595 (GRCm39) missense probably damaging 1.00
R2148:Cyp2j11 UTSW 4 96,204,595 (GRCm39) missense probably damaging 1.00
R2150:Cyp2j11 UTSW 4 96,204,595 (GRCm39) missense probably damaging 1.00
R4963:Cyp2j11 UTSW 4 96,204,619 (GRCm39) missense probably damaging 1.00
R5335:Cyp2j11 UTSW 4 96,195,589 (GRCm39) missense probably damaging 1.00
R5450:Cyp2j11 UTSW 4 96,228,113 (GRCm39) missense probably benign 0.44
R5688:Cyp2j11 UTSW 4 96,233,358 (GRCm39) missense probably damaging 1.00
R5978:Cyp2j11 UTSW 4 96,207,589 (GRCm39) missense probably damaging 1.00
R6061:Cyp2j11 UTSW 4 96,236,853 (GRCm39) start gained probably benign
R6075:Cyp2j11 UTSW 4 96,233,322 (GRCm39) missense probably benign 0.04
R6912:Cyp2j11 UTSW 4 96,183,108 (GRCm39) missense probably benign 0.00
R7338:Cyp2j11 UTSW 4 96,195,524 (GRCm39) missense possibly damaging 0.64
R7394:Cyp2j11 UTSW 4 96,204,677 (GRCm39) missense probably benign 0.00
R7464:Cyp2j11 UTSW 4 96,233,357 (GRCm39) missense probably damaging 1.00
R7972:Cyp2j11 UTSW 4 96,185,871 (GRCm39) missense probably damaging 1.00
R8152:Cyp2j11 UTSW 4 96,195,529 (GRCm39) missense probably damaging 1.00
R8328:Cyp2j11 UTSW 4 96,236,605 (GRCm39) missense probably benign 0.03
R8383:Cyp2j11 UTSW 4 96,236,695 (GRCm39) missense probably benign 0.00
R8519:Cyp2j11 UTSW 4 96,207,539 (GRCm39) missense probably benign 0.44
R8789:Cyp2j11 UTSW 4 96,227,405 (GRCm39) missense probably damaging 0.99
R9268:Cyp2j11 UTSW 4 96,207,781 (GRCm39) intron probably benign
R9323:Cyp2j11 UTSW 4 96,195,619 (GRCm39) missense probably benign 0.01
R9457:Cyp2j11 UTSW 4 96,195,596 (GRCm39) missense probably damaging 0.98
R9590:Cyp2j11 UTSW 4 96,195,614 (GRCm39) missense probably benign 0.11
Z1176:Cyp2j11 UTSW 4 96,195,673 (GRCm39) missense probably damaging 0.99
Z1176:Cyp2j11 UTSW 4 96,195,540 (GRCm39) missense probably damaging 0.99
Posted On 2014-02-04