Incidental Mutation 'IGL02720:Cyp4a12b'
ID 304984
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp4a12b
Ensembl Gene ENSMUSG00000078597
Gene Name cytochrome P450, family 4, subfamily a, polypeptide 12B
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL02720
Quality Score
Status
Chromosome 4
Chromosomal Location 115268821-115296231 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 115292368 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000092487 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094887]
AlphaFold A2A974
Predicted Effect probably benign
Transcript: ENSMUST00000094887
SMART Domains Protein: ENSMUSP00000092487
Gene: ENSMUSG00000078597

DomainStartEndE-ValueType
low complexity region 18 39 N/A INTRINSIC
Pfam:p450 51 503 1.9e-132 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass G A 6: 23,122,702 (GRCm39) probably benign Het
Adgrv1 A G 13: 81,726,991 (GRCm39) S454P probably damaging Het
Adh4 A T 3: 138,124,981 (GRCm39) I51F possibly damaging Het
Amigo2 A T 15: 97,143,578 (GRCm39) C281* probably null Het
Btn2a2 C T 13: 23,664,637 (GRCm39) R307Q probably benign Het
C2cd6 T C 1: 59,090,307 (GRCm39) I483M probably damaging Het
Capn9 T C 8: 125,327,236 (GRCm39) probably benign Het
Carmil3 A G 14: 55,744,867 (GRCm39) K1279E probably damaging Het
Cdadc1 T C 14: 59,823,496 (GRCm39) Y332C probably damaging Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cep112 T G 11: 108,750,177 (GRCm39) F893L probably damaging Het
Cit A G 5: 116,133,511 (GRCm39) S1867G probably benign Het
Clptm1l T C 13: 73,762,721 (GRCm39) probably benign Het
Dlx3 G T 11: 95,014,470 (GRCm39) W251L possibly damaging Het
Dnah1 C T 14: 30,984,177 (GRCm39) V3993M probably damaging Het
Efs A T 14: 55,157,172 (GRCm39) Y380N probably damaging Het
Fam53c T A 18: 34,903,720 (GRCm39) W331R probably damaging Het
Gm5414 T C 15: 101,533,990 (GRCm39) E331G probably damaging Het
Gstcd A G 3: 132,777,722 (GRCm39) V363A probably benign Het
Jak1 A G 4: 101,021,647 (GRCm39) probably benign Het
Kifc3 A G 8: 95,834,993 (GRCm39) V264A probably benign Het
Mapk8ip2 A G 15: 89,341,785 (GRCm39) D332G probably damaging Het
Nbeal1 G A 1: 60,323,146 (GRCm39) E2075K probably damaging Het
Opn5 T G 17: 42,907,517 (GRCm39) S120R probably damaging Het
Or52m2 C T 7: 102,264,046 (GRCm39) G50E probably damaging Het
Paqr8 C T 1: 21,005,733 (GRCm39) Q296* probably null Het
Pcsk6 C T 7: 65,629,995 (GRCm39) R374* probably null Het
Pld1 A G 3: 28,141,411 (GRCm39) H469R probably damaging Het
Rbl1 A G 2: 157,041,349 (GRCm39) S93P possibly damaging Het
Reln C T 5: 22,202,939 (GRCm39) R1287Q probably damaging Het
Rev3l C T 10: 39,698,391 (GRCm39) R963* probably null Het
Serinc4 C T 2: 121,282,908 (GRCm39) S418N probably benign Het
Slc6a18 A G 13: 73,818,087 (GRCm39) M310T probably benign Het
Slitrk3 T A 3: 72,958,101 (GRCm39) S224C probably damaging Het
Slu7 T C 11: 43,336,030 (GRCm39) I471T probably benign Het
Stxbp5 A G 10: 9,665,105 (GRCm39) probably null Het
Tm7sf3 A T 6: 146,514,872 (GRCm39) probably benign Het
Trem1 C T 17: 48,539,869 (GRCm39) S16L probably benign Het
Trp53bp2 T A 1: 182,281,289 (GRCm39) D963E probably benign Het
Trp63 A T 16: 25,682,491 (GRCm39) D184V probably damaging Het
Ttll6 T C 11: 96,042,899 (GRCm39) probably null Het
Usp32 A G 11: 84,897,817 (GRCm39) probably null Het
Vmn2r14 A T 5: 109,369,305 (GRCm39) N89K probably damaging Het
Vmn2r76 T C 7: 85,874,914 (GRCm39) R688G probably benign Het
Vmn2r93 A T 17: 18,525,296 (GRCm39) H318L probably damaging Het
Vstm4 A G 14: 32,585,574 (GRCm39) H47R probably damaging Het
Wdr55 A G 18: 36,896,435 (GRCm39) E375G probably benign Het
Ybx2 T A 11: 69,831,157 (GRCm39) S56T probably benign Het
Ybx2 C A 11: 69,831,158 (GRCm39) S251Y probably benign Het
Zbtb3 T C 19: 8,781,578 (GRCm39) probably null Het
Other mutations in Cyp4a12b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00850:Cyp4a12b APN 4 115,295,246 (GRCm39) splice site probably null
IGL01571:Cyp4a12b APN 4 115,295,354 (GRCm39) missense probably benign 0.00
IGL02230:Cyp4a12b APN 4 115,291,193 (GRCm39) missense probably damaging 1.00
IGL03118:Cyp4a12b APN 4 115,290,173 (GRCm39) missense possibly damaging 0.54
IGL03389:Cyp4a12b APN 4 115,291,005 (GRCm39) missense possibly damaging 0.90
R0360:Cyp4a12b UTSW 4 115,290,117 (GRCm39) missense probably benign 0.01
R0364:Cyp4a12b UTSW 4 115,290,117 (GRCm39) missense probably benign 0.01
R0844:Cyp4a12b UTSW 4 115,289,721 (GRCm39) missense possibly damaging 0.67
R1226:Cyp4a12b UTSW 4 115,290,164 (GRCm39) missense possibly damaging 0.80
R1232:Cyp4a12b UTSW 4 115,289,760 (GRCm39) missense possibly damaging 0.81
R1372:Cyp4a12b UTSW 4 115,290,146 (GRCm39) missense probably benign 0.08
R1559:Cyp4a12b UTSW 4 115,291,181 (GRCm39) missense probably damaging 0.98
R1782:Cyp4a12b UTSW 4 115,291,178 (GRCm39) missense probably damaging 1.00
R1817:Cyp4a12b UTSW 4 115,271,259 (GRCm39) splice site probably benign
R1941:Cyp4a12b UTSW 4 115,295,256 (GRCm39) missense probably damaging 1.00
R1978:Cyp4a12b UTSW 4 115,295,342 (GRCm39) missense probably benign 0.01
R2063:Cyp4a12b UTSW 4 115,290,700 (GRCm39) missense possibly damaging 0.87
R2109:Cyp4a12b UTSW 4 115,290,110 (GRCm39) missense probably damaging 0.97
R2911:Cyp4a12b UTSW 4 115,290,723 (GRCm39) nonsense probably null
R3791:Cyp4a12b UTSW 4 115,292,167 (GRCm39) missense probably benign 0.01
R3815:Cyp4a12b UTSW 4 115,289,667 (GRCm39) missense probably damaging 0.98
R3816:Cyp4a12b UTSW 4 115,289,667 (GRCm39) missense probably damaging 0.98
R3817:Cyp4a12b UTSW 4 115,289,667 (GRCm39) missense probably damaging 0.98
R3818:Cyp4a12b UTSW 4 115,289,667 (GRCm39) missense probably damaging 0.98
R4586:Cyp4a12b UTSW 4 115,289,703 (GRCm39) missense probably damaging 1.00
R5004:Cyp4a12b UTSW 4 115,295,310 (GRCm39) missense probably benign 0.39
R5105:Cyp4a12b UTSW 4 115,290,958 (GRCm39) missense probably damaging 1.00
R5354:Cyp4a12b UTSW 4 115,290,661 (GRCm39) splice site probably null
R5655:Cyp4a12b UTSW 4 115,290,994 (GRCm39) missense probably damaging 1.00
R5814:Cyp4a12b UTSW 4 115,289,694 (GRCm39) missense probably damaging 0.97
R5952:Cyp4a12b UTSW 4 115,271,714 (GRCm39) nonsense probably null
R6004:Cyp4a12b UTSW 4 115,290,664 (GRCm39) missense probably benign 0.35
R6059:Cyp4a12b UTSW 4 115,295,301 (GRCm39) missense possibly damaging 0.94
R6261:Cyp4a12b UTSW 4 115,271,740 (GRCm39) nonsense probably null
R7484:Cyp4a12b UTSW 4 115,289,760 (GRCm39) missense possibly damaging 0.81
R7734:Cyp4a12b UTSW 4 115,268,937 (GRCm39) missense possibly damaging 0.89
R8545:Cyp4a12b UTSW 4 115,290,227 (GRCm39) missense probably benign 0.23
R9031:Cyp4a12b UTSW 4 115,290,865 (GRCm39) missense probably benign 0.00
R9497:Cyp4a12b UTSW 4 115,271,768 (GRCm39) missense probably benign 0.36
RF045:Cyp4a12b UTSW 4 115,289,690 (GRCm39) missense probably benign 0.23
Posted On 2015-04-16