Incidental Mutation 'R6386:Cyp4a29'
ID 515596
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 044535-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # R6386 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 115099281-115111754 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to G at 115104272 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139717 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000118278] [ENSMUST00000118278]
AlphaFold A0A087WPC3
Predicted Effect probably null
Transcript: ENSMUST00000118278
SMART Domains Protein: ENSMUSP00000139717
Gene: ENSMUSG00000083138

DomainStartEndE-ValueType
transmembrane domain 9 31 N/A INTRINSIC
Pfam:p450 51 504 1.1e-127 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000118278
SMART Domains Protein: ENSMUSP00000139717
Gene: ENSMUSG00000083138

DomainStartEndE-ValueType
transmembrane domain 9 31 N/A INTRINSIC
Pfam:p450 51 504 1.1e-127 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.1%
  • 20x: 96.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ak6 TGACGA TGA 13: 100,792,311 (GRCm39) probably benign Het
Arap2 A T 5: 62,761,865 (GRCm39) N1620K possibly damaging Het
Atf6b T C 17: 34,870,825 (GRCm39) S396P probably damaging Het
Cc2d1a A G 8: 84,865,166 (GRCm39) M469T probably damaging Het
Ceacam3 A G 7: 16,892,144 (GRCm39) N296D probably benign Het
Cep57l1 A T 10: 41,619,128 (GRCm39) S80T probably damaging Het
Clip4 C A 17: 72,141,189 (GRCm39) Y514* probably null Het
Cop1 T C 1: 159,116,601 (GRCm39) I125T probably damaging Het
Cstf1 T C 2: 172,219,816 (GRCm39) V309A probably damaging Het
F830045P16Rik G A 2: 129,314,738 (GRCm39) H180Y probably damaging Het
Foxp4 T C 17: 48,189,387 (GRCm39) K237E unknown Het
Fstl5 A T 3: 76,229,373 (GRCm39) H58L probably benign Het
Gje1 A G 10: 14,592,365 (GRCm39) F139S probably damaging Het
Gpatch1 T C 7: 34,991,265 (GRCm39) D593G probably damaging Het
Inpp5d T A 1: 87,627,397 (GRCm39) L566Q probably damaging Het
Mtch2 A G 2: 90,679,739 (GRCm39) T38A probably benign Het
Mvb12b A T 2: 33,717,754 (GRCm39) I129N probably damaging Het
Npffr2 T C 5: 89,730,556 (GRCm39) V162A probably benign Het
Or4d10b A T 19: 12,036,920 (GRCm39) N65K probably damaging Het
Or5p61 A T 7: 107,758,409 (GRCm39) Y224N probably damaging Het
Pkhd1 G A 1: 20,621,244 (GRCm39) R805C probably damaging Het
Ppp4r4 T C 12: 103,559,364 (GRCm39) L406P probably damaging Het
Prl3d2 A G 13: 27,311,286 (GRCm39) D186G probably damaging Het
Rfc5 T C 5: 117,523,463 (GRCm39) T112A probably benign Het
Rnf148 A G 6: 23,654,483 (GRCm39) L171P probably damaging Het
Rps24 G A 14: 24,542,116 (GRCm39) G71S possibly damaging Het
Slco2a1 G A 9: 102,954,187 (GRCm39) V453I probably benign Het
Spidr T C 16: 15,786,424 (GRCm39) K440E probably benign Het
Syndig1 C A 2: 149,741,496 (GRCm39) N27K probably damaging Het
Tmem62 C T 2: 120,829,595 (GRCm39) T316I probably benign Het
Tpgs2 A T 18: 25,272,081 (GRCm39) I258N possibly damaging Het
Vmn2r78 A T 7: 86,571,545 (GRCm39) R452* probably null Het
Wasf3 A T 5: 146,390,227 (GRCm39) I124F possibly damaging Het
Wbp11 T C 6: 136,797,523 (GRCm39) T299A probably benign Het
Wdr25 T C 12: 108,990,991 (GRCm39) S41P probably damaging Het
Zfp874b T C 13: 67,622,962 (GRCm39) D116G possibly damaging 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
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
R9790:Cyp4a29 UTSW 4 115,108,380 (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'- TACTTCCAGCCTGTTCAAGATG -3'
(R):5'- CTGTTAAAGGGATGTCTCAAACCC -3'

Sequencing Primer
(F):5'- TCCAGCCTGTTCAAGATGATATC -3'
(R):5'- CGACAAATTTTCTAGCTAGTCAACTG -3'
Posted On 2018-05-04