Incidental Mutation 'IGL03493:Cyp4a31'
ID 490733
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp4a31
Ensembl Gene ENSMUSG00000028712
Gene Name cytochrome P450, family 4, subfamily a, polypeptide 31
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL03493
Quality Score
Status
Chromosome 4
Chromosomal Location 115420846-115436212 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 115427952 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000117129 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030480] [ENSMUST00000030486] [ENSMUST00000126645] [ENSMUST00000141033]
AlphaFold F8WGU9
Predicted Effect probably null
Transcript: ENSMUST00000030480
SMART Domains Protein: ENSMUSP00000030480
Gene: ENSMUSG00000028712

DomainStartEndE-ValueType
transmembrane domain 13 35 N/A INTRINSIC
Pfam:p450 51 415 3.6e-97 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000030486
SMART Domains Protein: ENSMUSP00000030486
Gene: ENSMUSG00000028712

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
Pfam:p450 51 504 2.6e-134 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000126645
SMART Domains Protein: ENSMUSP00000117129
Gene: ENSMUSG00000028712

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
Pfam:p450 51 340 4.3e-66 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000141033
SMART Domains Protein: ENSMUSP00000115628
Gene: ENSMUSG00000028712

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
Pfam:p450 51 155 2.9e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldoart1 G A 4: 72,769,884 (GRCm39) T253I probably damaging Het
Ampd2 T C 3: 107,982,674 (GRCm39) E694G probably damaging Het
Atcay C A 10: 81,046,407 (GRCm39) E306* probably null Het
Atp13a5 G T 16: 29,116,342 (GRCm39) D546E probably benign Het
C2cd2 T C 16: 97,682,861 (GRCm39) D125G probably damaging Het
Col23a1 T C 11: 51,455,632 (GRCm39) probably null Het
Col9a1 T A 1: 24,260,651 (GRCm39) probably benign Het
Dnah11 G A 12: 117,976,533 (GRCm39) R2708C probably benign Het
Dzip3 T C 16: 48,772,059 (GRCm39) I537V probably benign Het
Ezh1 T C 11: 101,094,617 (GRCm39) T392A probably benign Het
Hsd17b14 A T 7: 45,205,515 (GRCm39) D42V probably damaging Het
Hsf2 A T 10: 57,381,462 (GRCm39) I294F probably damaging Het
Ibtk G T 9: 85,600,972 (GRCm39) S797R probably benign Het
Kif20b T A 19: 34,936,950 (GRCm39) C183* probably null Het
Lnpep G T 17: 17,799,433 (GRCm39) A74E probably damaging Het
Map4k1 A T 7: 28,683,576 (GRCm39) probably benign Het
Matn1 A G 4: 130,677,309 (GRCm39) R173G probably benign Het
Nyap1 A G 5: 137,733,278 (GRCm39) I585T probably damaging Het
Or13a27 A T 7: 139,925,066 (GRCm39) Y279N probably damaging Het
Or52e7 A G 7: 104,685,151 (GRCm39) T249A probably damaging Het
Or5d39 G A 2: 87,980,280 (GRCm39) P28S probably benign Het
Phactr2 A G 10: 13,133,413 (GRCm39) V190A probably benign Het
Podnl1 G A 8: 84,858,818 (GRCm39) V548I probably benign Het
Rad51c A T 11: 87,288,579 (GRCm39) H201Q probably benign Het
Sec63 C A 10: 42,704,937 (GRCm39) D730E probably benign Het
Smarcc2 A G 10: 128,297,226 (GRCm39) I39M probably damaging Het
Trav2 A G 14: 52,804,745 (GRCm39) probably benign Het
Ugt3a1 A G 15: 9,361,569 (GRCm39) Y115C probably damaging Het
Zfp955b T G 17: 33,521,519 (GRCm39) H329Q probably benign Het
Other mutations in Cyp4a31
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00429:Cyp4a31 APN 4 115,432,171 (GRCm39) unclassified probably benign
IGL01682:Cyp4a31 APN 4 115,435,228 (GRCm39) missense probably damaging 0.97
IGL02112:Cyp4a31 APN 4 115,428,180 (GRCm39) missense probably damaging 1.00
IGL02292:Cyp4a31 APN 4 115,423,698 (GRCm39) missense probably damaging 0.98
IGL02343:Cyp4a31 APN 4 115,421,026 (GRCm39) missense probably damaging 1.00
IGL02508:Cyp4a31 APN 4 115,428,261 (GRCm39) missense probably damaging 1.00
IGL03094:Cyp4a31 APN 4 115,435,305 (GRCm39) utr 3 prime probably benign
R0400:Cyp4a31 UTSW 4 115,420,915 (GRCm39) start codon destroyed probably null 1.00
R1263:Cyp4a31 UTSW 4 115,431,908 (GRCm39) missense probably benign 0.01
R1508:Cyp4a31 UTSW 4 115,422,250 (GRCm39) missense possibly damaging 0.53
R1523:Cyp4a31 UTSW 4 115,426,951 (GRCm39) missense probably benign 0.23
R1822:Cyp4a31 UTSW 4 115,423,810 (GRCm39) splice site probably null
R1832:Cyp4a31 UTSW 4 115,426,928 (GRCm39) missense probably benign
R1872:Cyp4a31 UTSW 4 115,431,933 (GRCm39) missense probably damaging 0.99
R2351:Cyp4a31 UTSW 4 115,428,510 (GRCm39) missense possibly damaging 0.95
R2426:Cyp4a31 UTSW 4 115,428,213 (GRCm39) missense probably damaging 0.98
R2993:Cyp4a31 UTSW 4 115,427,017 (GRCm39) missense probably benign 0.03
R3743:Cyp4a31 UTSW 4 115,423,716 (GRCm39) missense possibly damaging 0.95
R3812:Cyp4a31 UTSW 4 115,423,706 (GRCm39) missense probably benign
R3963:Cyp4a31 UTSW 4 115,431,969 (GRCm39) unclassified probably benign
R4211:Cyp4a31 UTSW 4 115,422,210 (GRCm39) missense probably benign 0.01
R4814:Cyp4a31 UTSW 4 115,427,466 (GRCm39) missense probably damaging 1.00
R6245:Cyp4a31 UTSW 4 115,428,545 (GRCm39) missense possibly damaging 0.91
R6255:Cyp4a31 UTSW 4 115,432,117 (GRCm39) missense possibly damaging 0.82
R6330:Cyp4a31 UTSW 4 115,421,074 (GRCm39) missense probably damaging 0.99
R6433:Cyp4a31 UTSW 4 115,427,466 (GRCm39) missense probably damaging 1.00
R6602:Cyp4a31 UTSW 4 115,426,904 (GRCm39) critical splice acceptor site probably null
R6844:Cyp4a31 UTSW 4 115,420,989 (GRCm39) missense probably null 0.00
R7154:Cyp4a31 UTSW 4 115,431,963 (GRCm39) critical splice donor site probably null
R7300:Cyp4a31 UTSW 4 115,427,468 (GRCm39) missense probably benign 0.03
R8188:Cyp4a31 UTSW 4 115,426,943 (GRCm39) missense probably benign 0.29
R8557:Cyp4a31 UTSW 4 115,427,438 (GRCm39) missense possibly damaging 0.93
R8692:Cyp4a31 UTSW 4 115,423,769 (GRCm39) missense probably damaging 0.98
R8696:Cyp4a31 UTSW 4 115,422,225 (GRCm39) missense probably benign 0.43
R8728:Cyp4a31 UTSW 4 115,422,225 (GRCm39) missense probably benign 0.43
R8753:Cyp4a31 UTSW 4 115,432,158 (GRCm39) missense probably benign 0.37
R8822:Cyp4a31 UTSW 4 115,422,225 (GRCm39) missense probably benign 0.43
R8942:Cyp4a31 UTSW 4 115,426,918 (GRCm39) missense possibly damaging 0.87
R9230:Cyp4a31 UTSW 4 115,428,281 (GRCm39) nonsense probably null
R9672:Cyp4a31 UTSW 4 115,427,422 (GRCm39) missense probably benign 0.05
X0020:Cyp4a31 UTSW 4 115,422,306 (GRCm39) missense probably benign 0.06
X0021:Cyp4a31 UTSW 4 115,435,158 (GRCm39) missense probably damaging 1.00
Posted On 2017-10-20