Incidental Mutation 'R9790:Cyp4a29'
ID 735862
Institutional Source Beutler Lab
Gene Symbol Cyp4a29
Ensembl Gene ENSMUSG00000083138
Gene Name cytochrome P450, family 4, subfamily a, polypeptide 29
Synonyms Cyp4a29-ps
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # R9790 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 115099281-115111754 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 115108380 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 368 (M368K)
Ref Sequence ENSEMBL: ENSMUSP00000139717 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000118278]
AlphaFold A0A087WPC3
Predicted Effect probably damaging
Transcript: ENSMUST00000118278
AA Change: M368K

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000139717
Gene: ENSMUSG00000083138
AA Change: M368K

DomainStartEndE-ValueType
transmembrane domain 9 31 N/A INTRINSIC
Pfam:p450 51 504 1.1e-127 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.3%
  • 20x: 98.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1a T C 5: 8,748,604 (GRCm39) Y312H probably damaging Het
Abcc10 A T 17: 46,633,185 (GRCm39) I549N probably damaging Het
Agpat2 A G 2: 26,486,395 (GRCm39) Y134H probably damaging Het
Alms1 A G 6: 85,596,425 (GRCm39) D417G probably benign Het
Apol11b T A 15: 77,519,475 (GRCm39) I202F probably benign Het
Arap1 C A 7: 101,037,376 (GRCm39) Q468K probably benign Het
Arhgef4 T C 1: 34,832,445 (GRCm39) probably null Het
Asap3 A T 4: 135,961,914 (GRCm39) N285I probably damaging Het
Aspm A T 1: 139,408,375 (GRCm39) I2421F probably damaging Het
Banp C A 8: 122,701,285 (GRCm39) D17E probably benign Het
Bsx T G 9: 40,788,905 (GRCm39) V154G probably damaging Het
Cacnb1 T C 11: 97,900,186 (GRCm39) D324G probably damaging Het
Ccdc170 A T 10: 4,483,957 (GRCm39) probably null Het
Ccdc187 T C 2: 26,171,227 (GRCm39) H417R probably benign Het
Cct4 T A 11: 22,949,070 (GRCm39) M272K probably damaging Het
Chd9 A G 8: 91,760,417 (GRCm39) E2054G possibly damaging Het
Ctnnal1 A T 4: 56,844,584 (GRCm39) S127T possibly damaging Het
Cttnbp2 T A 6: 18,376,027 (GRCm39) H1504L probably benign Het
Dhx32 A G 7: 133,326,267 (GRCm39) F527L probably benign Het
Foxk1 T C 5: 142,387,739 (GRCm39) V154A probably damaging Het
Frem3 G A 8: 81,339,890 (GRCm39) E728K probably benign Het
Garem2 C A 5: 30,319,747 (GRCm39) A403E probably benign Het
Gemin5 G A 11: 58,020,846 (GRCm39) Q1114* probably null Het
Gm11567 C T 11: 99,770,274 (GRCm39) R71C unknown Het
Gm13272 T C 4: 88,698,442 (GRCm39) V119A probably benign Het
Gpc6 T A 14: 117,163,435 (GRCm39) C30S probably damaging Het
Gprc6a A C 10: 51,491,395 (GRCm39) F785V probably damaging Het
Hormad1 T C 3: 95,494,693 (GRCm39) V368A probably benign Het
Hsd17b4 G A 18: 50,324,907 (GRCm39) probably null Het
Idh2 TCCCAGG T 7: 79,748,079 (GRCm39) probably benign Het
Il17ra C T 6: 120,459,240 (GRCm39) S797F probably damaging Het
Jmjd6 A G 11: 116,733,438 (GRCm39) S80P probably benign Het
Klhdc2 T A 12: 69,346,995 (GRCm39) N53K probably benign Het
Klhl30 C T 1: 91,282,089 (GRCm39) P230L probably benign Het
Marchf1 C A 8: 66,729,339 (GRCm39) A46E probably benign Het
Mast4 T C 13: 102,890,705 (GRCm39) T1050A probably benign Het
Mpp7 T C 18: 7,355,049 (GRCm39) N459S probably benign Het
Mtfr1l A G 4: 134,258,063 (GRCm39) V53A probably benign Het
Myh11 T A 16: 14,025,992 (GRCm39) E1326V Het
Myh3 A G 11: 66,992,005 (GRCm39) E1850G probably damaging Het
Myo16 A G 8: 10,619,925 (GRCm39) D1492G unknown Het
Myo3b C A 2: 70,180,287 (GRCm39) H1219Q probably benign Het
Nphp4 A T 4: 152,646,605 (GRCm39) Q1379L probably null Het
Or8g30 C T 9: 39,230,815 (GRCm39) V32I probably benign Het
Or9q1 A G 19: 13,804,914 (GRCm39) I282T probably benign Het
Osbpl6 T G 2: 76,385,361 (GRCm39) L265R probably damaging Het
Pld4 A G 12: 112,734,862 (GRCm39) T440A probably damaging Het
Prr14 T C 7: 127,071,128 (GRCm39) M1T probably null Het
Ptger4 A T 15: 5,273,178 (GRCm39) M1K probably null Het
Ptpn22 A T 3: 103,795,842 (GRCm39) T608S possibly damaging Het
S1pr2 A G 9: 20,879,319 (GRCm39) W170R probably damaging Het
Specc1l A G 10: 75,066,603 (GRCm39) I17M probably benign Het
Spmap1 T A 11: 97,666,594 (GRCm39) I31F probably benign Het
Sptbn4 C G 7: 27,071,662 (GRCm39) G1601R probably damaging Het
Sqor C T 2: 122,626,912 (GRCm39) P11L probably benign Het
Stac2 T C 11: 97,934,449 (GRCm39) D85G probably benign Het
Svs5 G A 2: 164,078,918 (GRCm39) Q330* probably null Het
Taar7e A G 10: 23,913,554 (GRCm39) I15V probably benign Het
Tcf4 A T 18: 69,770,007 (GRCm39) Y275F probably damaging Het
Tenm4 A G 7: 96,538,046 (GRCm39) N1873S probably damaging Het
Tert T A 13: 73,775,648 (GRCm39) V133D probably benign Het
Tfap2a T A 13: 40,870,658 (GRCm39) N410I probably damaging Het
Tjp3 A T 10: 81,109,694 (GRCm39) D836E probably benign Het
Tox3 A T 8: 90,975,206 (GRCm39) M475K unknown Het
Traf4 A T 11: 78,050,979 (GRCm39) D392E probably damaging Het
Vav2 A G 2: 27,181,825 (GRCm39) L338P probably damaging Het
Vmn1r81 T C 7: 11,994,113 (GRCm39) N165S probably benign Het
Vmn2r9 A T 5: 108,995,409 (GRCm39) V413E probably damaging Het
Wdr7 A T 18: 63,911,059 (GRCm39) D817V probably damaging Het
Zbtb38 G A 9: 96,570,700 (GRCm39) S128L probably damaging Het
Zfhx4 T A 3: 5,464,922 (GRCm39) H1718Q probably damaging Het
Zfp945 G A 17: 23,071,228 (GRCm39) H245Y probably benign Het
Other mutations in Cyp4a29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02687:Cyp4a29 APN 4 115,108,397 (GRCm39) missense probably damaging 0.99
IGL03224:Cyp4a29 APN 4 115,104,247 (GRCm39) missense probably damaging 0.97
IGL03271:Cyp4a29 APN 4 115,111,705 (GRCm39) missense probably damaging 1.00
IGL03387:Cyp4a29 APN 4 115,108,368 (GRCm39) missense possibly damaging 0.70
R0304:Cyp4a29 UTSW 4 115,110,129 (GRCm39) splice site probably benign
R2656:Cyp4a29 UTSW 4 115,106,921 (GRCm39) missense possibly damaging 0.95
R4012:Cyp4a29 UTSW 4 115,105,707 (GRCm39) missense probably benign
R4834:Cyp4a29 UTSW 4 115,106,867 (GRCm39) missense probably benign 0.00
R4856:Cyp4a29 UTSW 4 115,110,078 (GRCm39) missense probably benign
R4886:Cyp4a29 UTSW 4 115,110,078 (GRCm39) missense probably benign
R4939:Cyp4a29 UTSW 4 115,104,873 (GRCm39) critical splice donor site probably null
R4967:Cyp4a29 UTSW 4 115,104,196 (GRCm39) missense probably benign 0.00
R5071:Cyp4a29 UTSW 4 115,104,860 (GRCm39) missense probably benign 0.00
R5072:Cyp4a29 UTSW 4 115,104,860 (GRCm39) missense probably benign 0.00
R5073:Cyp4a29 UTSW 4 115,104,860 (GRCm39) missense probably benign 0.00
R5620:Cyp4a29 UTSW 4 115,108,088 (GRCm39) missense probably benign 0.12
R5818:Cyp4a29 UTSW 4 115,104,229 (GRCm39) missense possibly damaging 0.89
R6219:Cyp4a29 UTSW 4 115,106,927 (GRCm39) missense probably damaging 0.99
R6318:Cyp4a29 UTSW 4 115,107,396 (GRCm39) missense probably benign 0.00
R6386:Cyp4a29 UTSW 4 115,104,272 (GRCm39) critical splice donor site probably null
R6456:Cyp4a29 UTSW 4 115,108,381 (GRCm39) missense probably benign 0.30
R7393:Cyp4a29 UTSW 4 115,099,393 (GRCm39) missense probably damaging 1.00
R7443:Cyp4a29 UTSW 4 115,105,756 (GRCm39) missense probably damaging 1.00
R7719:Cyp4a29 UTSW 4 115,108,137 (GRCm39) missense possibly damaging 0.65
R7831:Cyp4a29 UTSW 4 115,107,367 (GRCm39) missense probably benign 0.00
R7983:Cyp4a29 UTSW 4 115,108,099 (GRCm39) missense probably damaging 1.00
R8304:Cyp4a29 UTSW 4 115,111,653 (GRCm39) missense probably damaging 1.00
R8674:Cyp4a29 UTSW 4 115,106,882 (GRCm39) missense probably benign 0.08
R9109:Cyp4a29 UTSW 4 115,108,395 (GRCm39) missense probably damaging 1.00
R9298:Cyp4a29 UTSW 4 115,108,395 (GRCm39) missense probably damaging 1.00
R9486:Cyp4a29 UTSW 4 115,106,916 (GRCm39) missense probably damaging 1.00
R9601:Cyp4a29 UTSW 4 115,105,772 (GRCm39) missense probably damaging 0.98
R9667:Cyp4a29 UTSW 4 115,111,630 (GRCm39) missense probably damaging 1.00
R9791:Cyp4a29 UTSW 4 115,108,380 (GRCm39) missense probably damaging 1.00
U24488:Cyp4a29 UTSW 4 115,108,204 (GRCm39) missense possibly damaging 0.95
Z1088:Cyp4a29 UTSW 4 115,105,693 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TTTGGCTACACATCCCGACC -3'
(R):5'- CTGCACAGATTTACTTACAAGGAG -3'

Sequencing Primer
(F):5'- CCACCAGCAGAGATGCAGAG -3'
(R):5'- GCACACAAAAAGATCCGATTTTTC -3'
Posted On 2022-11-14