Incidental Mutation 'IGL02814:Cyp4f37'
ID360690
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp4f37
Ensembl Gene ENSMUSG00000062464
Gene Namecytochrome P450, family 4, subfamily f, polypeptide 37
SynonymsGm9705
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.080) question?
Stock #IGL02814
Quality Score
Status
Chromosome17
Chromosomal Location32621319-32636184 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 32634671 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Serine at position 443 (F443S)
Ref Sequence ENSEMBL: ENSMUSP00000076827 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077639]
Predicted Effect probably benign
Transcript: ENSMUST00000077639
AA Change: F443S

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000076827
Gene: ENSMUSG00000062464
AA Change: F443S

DomainStartEndE-ValueType
Pfam:p450 52 515 1.1e-136 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700081O15Rik C A 19: 7,420,422 N111K possibly damaging Het
Abca9 A T 11: 110,154,467 F347I possibly damaging Het
Adcy5 A G 16: 35,303,649 T1233A probably benign Het
Blnk C T 19: 40,962,429 D93N probably damaging Het
Cadps2 T C 6: 23,321,707 E1083G probably damaging Het
Capn8 C A 1: 182,598,771 L224M probably damaging Het
Cdh4 A T 2: 179,780,474 E130D probably benign Het
Cgn G A 3: 94,774,240 T515M probably benign Het
Chrna10 C T 7: 102,112,262 G374D probably benign Het
Chrnb1 T A 11: 69,795,680 Y38F probably damaging Het
Cyld A G 8: 88,744,897 D621G probably benign Het
Dctn1 C A 6: 83,189,914 A152E probably damaging Het
Eml4 T A 17: 83,441,362 Y228* probably null Het
Fbln2 T A 6: 91,265,857 C846* probably null Het
Fut2 C T 7: 45,650,769 G193E possibly damaging Het
Gart T C 16: 91,623,457 S833G possibly damaging Het
Gda T C 19: 21,428,475 probably null Het
Gjb5 C T 4: 127,355,562 R263Q probably benign Het
Gtf2i T C 5: 134,286,704 K193E probably damaging Het
Hist2h4 C A 3: 96,263,287 K6N probably benign Het
Ints1 C T 5: 139,772,391 E244K possibly damaging Het
Kat14 G A 2: 144,402,463 S412N probably benign Het
Kcnn3 A T 3: 89,521,175 H236L possibly damaging Het
Kif15 T A 9: 123,003,640 I1005K possibly damaging Het
Klrc1 T C 6: 129,678,892 T7A possibly damaging Het
Lcp2 T C 11: 34,071,033 S130P probably damaging Het
Ldha T A 7: 46,850,891 Y133* probably null Het
Lrp2 A G 2: 69,506,736 C1231R probably damaging Het
Lrrn1 T A 6: 107,567,352 V37D probably damaging Het
Mep1a T A 17: 43,477,221 H648L probably benign Het
Mmp25 C T 17: 23,639,762 G272R probably damaging Het
Myh15 A G 16: 49,145,438 probably benign Het
Myl3 G T 9: 110,767,991 E140* probably null Het
Nlrp4f A G 13: 65,185,042 S809P probably damaging Het
Nrde2 T C 12: 100,144,135 I207M probably null Het
Olfr1373 C T 11: 52,144,810 C240Y probably damaging Het
Olfr474 T C 7: 107,954,770 I43T probably benign Het
Olfr541 T C 7: 140,705,133 L294P probably damaging Het
Paics T G 5: 76,962,473 V245G probably damaging Het
Pank1 A G 19: 34,840,855 F95L probably damaging Het
Pde4dip A C 3: 97,767,100 C167G probably damaging Het
Picalm C A 7: 90,191,749 T542K possibly damaging Het
Piezo1 A G 8: 122,498,215 Y651H probably damaging Het
Pikfyve T A 1: 65,250,194 C1208* probably null Het
Pkd1l1 T A 11: 8,902,582 T634S probably benign Het
Rab32 T C 10: 10,546,427 T183A probably benign Het
Rad18 T C 6: 112,644,622 I206V possibly damaging Het
Rbm15b T C 9: 106,885,776 I398V probably benign Het
Rbm28 T C 6: 29,159,726 E101G probably benign Het
Rsf1 T C 7: 97,661,227 L388P probably damaging Het
Scnn1g A G 7: 121,740,365 Y129C probably damaging Het
Slc7a13 G A 4: 19,839,387 C330Y probably benign Het
Spock1 A T 13: 57,587,673 V101E probably damaging Het
Sympk T A 7: 19,053,273 W1029R probably damaging Het
Syne2 T A 12: 75,945,376 H2008Q possibly damaging Het
Tgs1 T A 4: 3,585,719 Y199N probably damaging Het
Trim10 T A 17: 36,877,336 C481* probably null Het
Vmn2r102 A G 17: 19,677,908 E395G probably damaging Het
Wfs1 A C 5: 36,967,669 V626G possibly damaging Het
Zfp689 A G 7: 127,445,021 S146P possibly damaging Het
Zfp786 T C 6: 47,819,841 H721R probably damaging Het
Other mutations in Cyp4f37
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01140:Cyp4f37 APN 17 32629053 missense probably benign 0.20
IGL01994:Cyp4f37 APN 17 32625176 nonsense probably null
IGL02073:Cyp4f37 APN 17 32627851 missense possibly damaging 0.59
IGL02145:Cyp4f37 APN 17 32630035 missense probably benign 0.43
IGL02873:Cyp4f37 APN 17 32625168 missense probably benign 0.00
IGL02937:Cyp4f37 APN 17 32625189 missense probably benign 0.00
IGL03170:Cyp4f37 APN 17 32625119 splice site probably benign
R0625:Cyp4f37 UTSW 17 32634678 missense probably damaging 1.00
R1774:Cyp4f37 UTSW 17 32629890 missense possibly damaging 0.59
R1871:Cyp4f37 UTSW 17 32634665 missense probably damaging 1.00
R2232:Cyp4f37 UTSW 17 32634270 missense probably benign 0.23
R2847:Cyp4f37 UTSW 17 32629125 missense probably damaging 1.00
R2848:Cyp4f37 UTSW 17 32629125 missense probably damaging 1.00
R4027:Cyp4f37 UTSW 17 32631672 missense probably benign 0.00
R4463:Cyp4f37 UTSW 17 32627736 critical splice acceptor site probably null
R4517:Cyp4f37 UTSW 17 32631592 missense probably benign 0.00
R4573:Cyp4f37 UTSW 17 32629087 missense probably benign 0.23
R4670:Cyp4f37 UTSW 17 32625152 missense probably benign
R5752:Cyp4f37 UTSW 17 32631332 missense probably damaging 1.00
R5930:Cyp4f37 UTSW 17 32629983 missense possibly damaging 0.79
R6248:Cyp4f37 UTSW 17 32629890 missense possibly damaging 0.59
R7412:Cyp4f37 UTSW 17 32629844 missense possibly damaging 0.87
R8066:Cyp4f37 UTSW 17 32635073 missense probably benign 0.21
X0057:Cyp4f37 UTSW 17 32625224 missense probably benign 0.01
Posted On2015-12-18