Incidental Mutation 'IGL03328:Cyp4f17'
ID 416755
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp4f17
Ensembl Gene ENSMUSG00000091586
Gene Name cytochrome P450, family 4, subfamily f, polypeptide 17
Synonyms EG208285
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL03328
Quality Score
Status
Chromosome 17
Chromosomal Location 32725404-32749132 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 32739600 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Arginine at position 174 (M174R)
Ref Sequence ENSEMBL: ENSMUSP00000129514 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165999]
AlphaFold G3UW78
Predicted Effect probably damaging
Transcript: ENSMUST00000165999
AA Change: M174R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129514
Gene: ENSMUSG00000091586
AA Change: M174R

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
Pfam:p450 52 515 3.5e-135 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acaca A T 11: 84,211,355 (GRCm39) M1556L probably benign Het
Aicda T G 6: 122,539,396 (GRCm39) D187E probably benign Het
Arfgap3 A C 15: 83,227,282 (GRCm39) F43L probably damaging Het
AW551984 T C 9: 39,508,412 (GRCm39) E368G probably damaging Het
Bbs4 T C 9: 59,251,401 (GRCm39) E33G probably damaging Het
Bcas1 T A 2: 170,208,316 (GRCm39) K437* probably null Het
Brwd1 A T 16: 95,803,925 (GRCm39) W2082R probably damaging Het
Card6 A T 15: 5,134,927 (GRCm39) probably benign Het
Cd200r4 A G 16: 44,653,882 (GRCm39) I226M possibly damaging Het
Cep57l1 T C 10: 41,619,148 (GRCm39) E73G probably damaging Het
Chaf1a T G 17: 56,370,374 (GRCm39) F613C probably damaging Het
Clybl G T 14: 122,639,406 (GRCm39) K323N probably damaging Het
Coa7 A G 4: 108,195,479 (GRCm39) D136G probably damaging Het
Col5a2 C A 1: 45,415,306 (GRCm39) V1478L possibly damaging Het
Ctnnd2 T C 15: 30,921,993 (GRCm39) probably benign Het
Dnah10 A T 5: 124,831,354 (GRCm39) D794V probably benign Het
Eapp A G 12: 54,738,878 (GRCm39) S87P probably benign Het
Efnb3 A G 11: 69,448,031 (GRCm39) I137T probably damaging Het
Eif4e T A 3: 138,259,488 (GRCm39) probably benign Het
Fam83b T A 9: 76,400,324 (GRCm39) I260L probably benign Het
Fras1 A G 5: 96,929,619 (GRCm39) T4008A probably damaging Het
Fut8 A T 12: 77,412,003 (GRCm39) R118W probably damaging Het
Glt1d1 A C 5: 127,734,183 (GRCm39) D119A probably benign Het
Gm3727 T A 14: 7,261,685 (GRCm38) *206C probably null Het
Gmip G A 8: 70,264,261 (GRCm39) V174M possibly damaging Het
Gtf2ird1 A G 5: 134,417,983 (GRCm39) probably null Het
Haao C T 17: 84,154,078 (GRCm39) C23Y probably damaging Het
Hip1 A T 5: 135,453,728 (GRCm39) V400E probably damaging Het
Keg1 A G 19: 12,696,461 (GRCm39) N215S probably damaging Het
Lss T G 10: 76,376,785 (GRCm39) I334S probably damaging Het
Lyn A C 4: 3,745,327 (GRCm39) E77D probably benign Het
Myo3a A G 2: 22,468,210 (GRCm39) E1426G probably benign Het
Ncapg2 A G 12: 116,403,677 (GRCm39) E863G possibly damaging Het
Ncl T C 1: 86,280,319 (GRCm39) Y496C probably damaging Het
Nefm A T 14: 68,358,739 (GRCm39) S432T probably benign Het
Nipsnap1 A G 11: 4,834,096 (GRCm39) Y95C possibly damaging Het
Npc1l1 C A 11: 6,168,643 (GRCm39) E913* probably null Het
Nup205 T C 6: 35,209,349 (GRCm39) L1552P probably damaging Het
Or2t46 A G 11: 58,472,539 (GRCm39) N290D probably damaging Het
Or4c112 G T 2: 88,854,199 (GRCm39) Y49* probably null Het
Or52h7 T A 7: 104,213,677 (GRCm39) V83D probably damaging Het
Or7c70 C T 10: 78,683,201 (GRCm39) E183K probably benign Het
Osm A C 11: 4,188,426 (GRCm39) I18L unknown Het
Otoa T A 7: 120,710,217 (GRCm39) S254R probably damaging Het
Parp1 T C 1: 180,427,155 (GRCm39) probably benign Het
Pcdh17 A G 14: 84,770,551 (GRCm39) I1010V probably benign Het
Peli2 A T 14: 48,490,032 (GRCm39) probably null Het
Pkd1l3 T G 8: 110,388,738 (GRCm39) probably benign Het
Pkhd1 A G 1: 20,151,524 (GRCm39) probably benign Het
Polg2 A C 11: 106,659,163 (GRCm39) V450G probably benign Het
Potegl A T 2: 23,102,817 (GRCm39) Y185F possibly damaging Het
Ptpn13 A T 5: 103,664,214 (GRCm39) T401S probably benign Het
Rgs22 C T 15: 36,043,350 (GRCm39) probably null Het
Rttn T G 18: 89,061,152 (GRCm39) S1107A probably benign Het
Scn5a G T 9: 119,366,702 (GRCm39) N328K probably benign Het
Sned1 G A 1: 93,217,089 (GRCm39) A1325T probably benign Het
St8sia4 T A 1: 95,588,595 (GRCm39) E80V probably benign Het
Stard7 T C 2: 127,134,176 (GRCm39) probably benign Het
Suco G T 1: 161,647,990 (GRCm39) P1099T probably damaging Het
Syn2 G T 6: 115,251,221 (GRCm39) C459F probably damaging Het
Tas2r117 A C 6: 132,780,041 (GRCm39) I60L probably benign Het
Tomm70a T C 16: 56,965,150 (GRCm39) C445R probably damaging Het
Tpsab1 T A 17: 25,564,102 (GRCm39) D87V probably benign Het
Trgc4 A G 13: 19,536,416 (GRCm39) Y158C unknown Het
Trpm6 A T 19: 18,815,446 (GRCm39) E1177D possibly damaging Het
Vmn2r71 A T 7: 85,273,499 (GRCm39) D771V probably damaging Het
Vmn2r93 A T 17: 18,525,220 (GRCm39) T293S probably damaging Het
Other mutations in Cyp4f17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00580:Cyp4f17 APN 17 32,743,849 (GRCm39) nonsense probably null
IGL01767:Cyp4f17 APN 17 32,725,956 (GRCm39) missense probably benign
IGL01867:Cyp4f17 APN 17 32,747,057 (GRCm39) missense probably benign 0.30
IGL02009:Cyp4f17 APN 17 32,743,854 (GRCm39) missense probably damaging 1.00
IGL02423:Cyp4f17 APN 17 32,725,923 (GRCm39) missense possibly damaging 0.93
IGL02503:Cyp4f17 APN 17 32,743,940 (GRCm39) critical splice donor site probably null
IGL02571:Cyp4f17 APN 17 32,743,878 (GRCm39) missense probably benign 0.42
IGL03047:Cyp4f17 UTSW 17 32,743,023 (GRCm39) missense possibly damaging 0.88
PIT4810001:Cyp4f17 UTSW 17 32,743,574 (GRCm39) missense possibly damaging 0.56
R0486:Cyp4f17 UTSW 17 32,743,797 (GRCm39) splice site probably benign
R0606:Cyp4f17 UTSW 17 32,746,817 (GRCm39) missense probably damaging 0.98
R0655:Cyp4f17 UTSW 17 32,743,871 (GRCm39) missense possibly damaging 0.95
R1781:Cyp4f17 UTSW 17 32,742,993 (GRCm39) missense possibly damaging 0.94
R1795:Cyp4f17 UTSW 17 32,736,943 (GRCm39) missense probably benign 0.00
R1833:Cyp4f17 UTSW 17 32,743,184 (GRCm39) missense probably benign 0.01
R2268:Cyp4f17 UTSW 17 32,736,928 (GRCm39) missense probably benign 0.44
R3030:Cyp4f17 UTSW 17 32,725,950 (GRCm39) missense possibly damaging 0.93
R3861:Cyp4f17 UTSW 17 32,747,078 (GRCm39) missense probably damaging 0.97
R5236:Cyp4f17 UTSW 17 32,739,606 (GRCm39) critical splice donor site probably null
R5450:Cyp4f17 UTSW 17 32,747,860 (GRCm39) missense probably benign
R5866:Cyp4f17 UTSW 17 32,725,887 (GRCm39) missense probably benign 0.03
R5886:Cyp4f17 UTSW 17 32,743,013 (GRCm39) missense possibly damaging 0.78
R5965:Cyp4f17 UTSW 17 32,743,611 (GRCm39) missense probably damaging 0.99
R6692:Cyp4f17 UTSW 17 32,725,950 (GRCm39) missense possibly damaging 0.93
R7056:Cyp4f17 UTSW 17 32,746,846 (GRCm39) missense possibly damaging 0.94
R7968:Cyp4f17 UTSW 17 32,743,116 (GRCm39) missense possibly damaging 0.87
R8458:Cyp4f17 UTSW 17 32,739,550 (GRCm39) missense probably damaging 1.00
R8550:Cyp4f17 UTSW 17 32,746,936 (GRCm39) missense probably benign 0.01
R8818:Cyp4f17 UTSW 17 32,743,068 (GRCm39) missense probably damaging 1.00
R9139:Cyp4f17 UTSW 17 32,743,868 (GRCm39) nonsense probably null
R9360:Cyp4f17 UTSW 17 32,743,880 (GRCm39) missense probably benign 0.25
R9375:Cyp4f17 UTSW 17 32,747,746 (GRCm39) missense probably damaging 0.97
R9690:Cyp4f17 UTSW 17 32,725,950 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02