Incidental Mutation 'R8303:Cyp4f37'
ID 639356
Institutional Source Beutler Lab
Gene Symbol Cyp4f37
Ensembl Gene ENSMUSG00000062464
Gene Name cytochrome P450, family 4, subfamily f, polypeptide 37
Synonyms Gm9705
MMRRC Submission 067715-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.222) question?
Stock # R8303 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 32840283-32855158 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) G to A at 32853152 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000076827 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077639] [ENSMUST00000077639]
AlphaFold Q3V1F1
Predicted Effect probably null
Transcript: ENSMUST00000077639
SMART Domains Protein: ENSMUSP00000076827
Gene: ENSMUSG00000062464

DomainStartEndE-ValueType
Pfam:p450 52 515 1.1e-136 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000077639
SMART Domains Protein: ENSMUSP00000076827
Gene: ENSMUSG00000062464

DomainStartEndE-ValueType
Pfam:p450 52 515 1.1e-136 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 100% (65/65)
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik T A 11: 58,770,966 (GRCm39) D149E probably benign Het
Aars2 T C 17: 45,818,523 (GRCm39) C103R probably damaging Het
Aass T C 6: 23,092,367 (GRCm39) D591G probably benign Het
Arhgap32 A G 9: 32,172,205 (GRCm39) T1662A probably benign Het
Arhgap42 A T 9: 9,009,327 (GRCm39) I520N probably damaging Het
Arhgef3 T C 14: 27,116,095 (GRCm39) I279T probably damaging Het
Arid4b A G 13: 14,294,808 (GRCm39) K30R probably damaging Het
Asxl3 C T 18: 22,657,473 (GRCm39) R1828W probably benign Het
Bid T C 6: 120,877,200 (GRCm39) Y47C probably benign Het
Card6 T C 15: 5,134,847 (GRCm39) T119A probably benign Het
Cbr1 T C 16: 93,406,905 (GRCm39) I207T probably damaging Het
Cep135 T C 5: 76,759,575 (GRCm39) L443P probably damaging Het
Cfap251 T A 5: 123,460,650 (GRCm39) V1204E probably damaging Het
Cfap43 T A 19: 47,754,274 (GRCm39) R1017* probably null Het
Cfap52 T A 11: 67,830,621 (GRCm39) S280C probably benign Het
Cntnap5b T C 1: 100,069,022 (GRCm39) F81L probably damaging Het
Cyp4a12a A G 4: 115,186,130 (GRCm39) D430G probably damaging Het
Dclre1a A G 19: 56,531,121 (GRCm39) S742P probably damaging Het
Ddx54 T C 5: 120,759,855 (GRCm39) F414S probably damaging Het
Dsp A G 13: 38,381,319 (GRCm39) N2688S probably benign Het
Elovl4 A T 9: 83,670,320 (GRCm39) probably null Het
Erbin A C 13: 103,966,694 (GRCm39) probably null Het
Fsip2 A G 2: 82,818,724 (GRCm39) D4819G probably benign Het
Gapvd1 G A 2: 34,602,212 (GRCm39) P645L probably damaging Het
Gbp9 T C 5: 105,229,171 (GRCm39) E492G possibly damaging Het
Gpc5 T A 14: 115,665,667 (GRCm39) I497K probably benign Het
Hlx A G 1: 184,459,905 (GRCm39) L411P probably damaging Het
Hmmr G A 11: 40,612,499 (GRCm39) S206F probably damaging Het
Ice1 A T 13: 70,754,526 (GRCm39) I520N probably benign Het
Ist1 T C 8: 110,410,412 (GRCm39) probably null Het
Itga3 T C 11: 94,953,466 (GRCm39) D292G probably benign Het
Kif21a T C 15: 90,855,399 (GRCm39) N655S probably damaging Het
Lrrtm1 A G 6: 77,221,662 (GRCm39) H373R probably benign Het
Ngdn A T 14: 55,260,602 (GRCm39) H270L probably benign Het
Nol4 G A 18: 23,173,231 (GRCm39) probably benign Het
Nup50l T C 6: 96,142,702 (GRCm39) E114G probably benign Het
Nxpe5 G A 5: 138,239,264 (GRCm39) probably benign Het
Or1j18 A G 2: 36,624,467 (GRCm39) I45V probably damaging Het
Or4c11c G A 2: 88,661,633 (GRCm39) M57I possibly damaging Het
Or8d1 A C 9: 38,766,837 (GRCm39) T160P probably damaging Het
Or8g30 A C 9: 39,230,689 (GRCm39) S74A probably damaging Het
Pask C A 1: 93,248,286 (GRCm39) R1005L probably benign Het
Pcm1 A G 8: 41,736,758 (GRCm39) T875A probably damaging Het
Pdrg1 A T 2: 152,851,587 (GRCm39) I130N probably damaging Het
Plec A T 15: 76,073,466 (GRCm39) M448K unknown Het
R3hdml T G 2: 163,341,832 (GRCm39) V204G probably damaging Het
Rasa4 G A 5: 136,118,235 (GRCm39) V32M possibly damaging Het
Scaf8 T C 17: 3,198,827 (GRCm39) V44A unknown Het
Smad3 G T 9: 63,574,760 (GRCm39) P177T probably benign Het
Smpd4 T A 16: 17,457,195 (GRCm39) F384L probably damaging Het
Sycp2l G C 13: 41,283,275 (GRCm39) L170F probably damaging Het
Tas2r107 T C 6: 131,636,585 (GRCm39) S155G probably benign Het
Tmem143 T A 7: 45,565,994 (GRCm39) M439K probably benign Het
Ttc41 A T 10: 86,555,494 (GRCm39) T317S probably benign Het
Umps A G 16: 33,784,240 (GRCm39) V71A possibly damaging Het
Usp17lc G A 7: 103,067,389 (GRCm39) G228D possibly damaging Het
Usp17ld C T 7: 102,900,023 (GRCm39) C303Y probably damaging Het
Vmn2r65 C A 7: 84,589,391 (GRCm39) E842* probably null Het
Vmn2r94 A G 17: 18,464,433 (GRCm39) F619S probably damaging Het
Vps13a T C 19: 16,594,270 (GRCm39) T3154A probably benign Het
Vps13b C T 15: 35,640,063 (GRCm39) T1311I probably damaging Het
Xpot A T 10: 121,447,405 (GRCm39) Y353* probably null Het
Zfp319 A T 8: 96,055,765 (GRCm39) L146Q probably damaging Het
Zfp422 T A 6: 116,603,612 (GRCm39) H129L probably damaging Het
Zzef1 T C 11: 72,808,015 (GRCm39) F2709L probably damaging Het
Other mutations in Cyp4f37
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01140:Cyp4f37 APN 17 32,848,027 (GRCm39) missense probably benign 0.20
IGL01994:Cyp4f37 APN 17 32,844,150 (GRCm39) nonsense probably null
IGL02073:Cyp4f37 APN 17 32,846,825 (GRCm39) missense possibly damaging 0.59
IGL02145:Cyp4f37 APN 17 32,849,009 (GRCm39) missense probably benign 0.43
IGL02814:Cyp4f37 APN 17 32,853,645 (GRCm39) missense probably benign 0.01
IGL02873:Cyp4f37 APN 17 32,844,142 (GRCm39) missense probably benign 0.00
IGL02937:Cyp4f37 APN 17 32,844,163 (GRCm39) missense probably benign 0.00
IGL03170:Cyp4f37 APN 17 32,844,093 (GRCm39) splice site probably benign
R0625:Cyp4f37 UTSW 17 32,853,652 (GRCm39) missense probably damaging 1.00
R1774:Cyp4f37 UTSW 17 32,848,864 (GRCm39) missense possibly damaging 0.59
R1871:Cyp4f37 UTSW 17 32,853,639 (GRCm39) missense probably damaging 1.00
R2232:Cyp4f37 UTSW 17 32,853,244 (GRCm39) missense probably benign 0.23
R2847:Cyp4f37 UTSW 17 32,848,099 (GRCm39) missense probably damaging 1.00
R2848:Cyp4f37 UTSW 17 32,848,099 (GRCm39) missense probably damaging 1.00
R4027:Cyp4f37 UTSW 17 32,850,646 (GRCm39) missense probably benign 0.00
R4463:Cyp4f37 UTSW 17 32,846,710 (GRCm39) critical splice acceptor site probably null
R4517:Cyp4f37 UTSW 17 32,850,566 (GRCm39) missense probably benign 0.00
R4573:Cyp4f37 UTSW 17 32,848,061 (GRCm39) missense probably benign 0.23
R4670:Cyp4f37 UTSW 17 32,844,126 (GRCm39) missense probably benign
R5752:Cyp4f37 UTSW 17 32,850,306 (GRCm39) missense probably damaging 1.00
R5930:Cyp4f37 UTSW 17 32,848,957 (GRCm39) missense possibly damaging 0.79
R6248:Cyp4f37 UTSW 17 32,848,864 (GRCm39) missense possibly damaging 0.59
R7412:Cyp4f37 UTSW 17 32,848,818 (GRCm39) missense possibly damaging 0.87
R7969:Cyp4f37 UTSW 17 32,844,181 (GRCm39) missense probably benign 0.00
R8066:Cyp4f37 UTSW 17 32,854,047 (GRCm39) missense probably benign 0.21
R8187:Cyp4f37 UTSW 17 32,854,171 (GRCm39) missense probably benign
R8309:Cyp4f37 UTSW 17 32,853,952 (GRCm39) missense probably damaging 1.00
R8407:Cyp4f37 UTSW 17 32,853,158 (GRCm39) missense probably damaging 1.00
R8869:Cyp4f37 UTSW 17 32,844,096 (GRCm39) missense probably benign 0.01
R9054:Cyp4f37 UTSW 17 32,853,253 (GRCm39) missense probably benign 0.25
R9565:Cyp4f37 UTSW 17 32,844,205 (GRCm39) missense possibly damaging 0.79
R9674:Cyp4f37 UTSW 17 32,846,841 (GRCm39) critical splice donor site probably null
X0057:Cyp4f37 UTSW 17 32,844,198 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- TGGCATCAAAACTTGGGAAGTG -3'
(R):5'- AGTACTAGCCAGGTCCAAGC -3'

Sequencing Primer
(F):5'- CAAATACAGGAGTTCAAGGTTGTTC -3'
(R):5'- TCCAAGCTGCCCCTAGAG -3'
Posted On 2020-07-28