Incidental Mutation 'IGL02191:Cyp51'
ID 283864
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp51
Ensembl Gene ENSMUSG00000001467
Gene Name cytochrome P450, family 51
Synonyms
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL02191
Quality Score
Status
Chromosome 5
Chromosomal Location 4131145-4154746 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 4150147 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Isoleucine at position 192 (R192I)
Ref Sequence ENSEMBL: ENSMUSP00000001507 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001507]
AlphaFold Q8K0C4
Predicted Effect probably benign
Transcript: ENSMUST00000001507
AA Change: R192I

PolyPhen 2 Score 0.047 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000001507
Gene: ENSMUSG00000001467
AA Change: R192I

DomainStartEndE-ValueType
transmembrane domain 21 43 N/A INTRINSIC
Pfam:p450 61 496 1.9e-76 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129448
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151539
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199909
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein participates in the synthesis of cholesterol by catalyzing the removal of the 14alpha-methyl group from lanosterol. Homologous genes are found in all three eukaryotic phyla, fungi, plants, and animals, suggesting that this is one of the oldest cytochrome P450 genes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit skeletal and craniofacial abnormalities and die at late midgestation due to heart failure resulting from cardiac hypoplasia, ventricle septum, epicardial and vasculogenesis defects. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn1 T C 12: 80,220,883 (GRCm39) I642V probably benign Het
Adam5 G A 8: 25,302,439 (GRCm39) R185* probably null Het
C2 T C 17: 35,085,539 (GRCm39) I122V probably damaging Het
Camsap1 A G 2: 25,819,892 (GRCm39) I1531T probably damaging Het
Celsr1 T C 15: 85,863,205 (GRCm39) T1276A possibly damaging Het
Cnot7 A T 8: 40,963,068 (GRCm39) N35K probably benign Het
Cyp2a12 A G 7: 26,736,036 (GRCm39) I482V probably benign Het
Cyp3a57 A G 5: 145,302,495 (GRCm39) E97G probably damaging Het
Ddx59 T C 1: 136,344,896 (GRCm39) L189P probably damaging Het
Dnah6 A G 6: 72,994,780 (GRCm39) I4127T probably benign Het
Dock3 C T 9: 106,815,340 (GRCm39) V1217I probably benign Het
Ergic2 T C 6: 148,106,319 (GRCm39) D57G probably null Het
Flvcr2 A T 12: 85,832,966 (GRCm39) K329* probably null Het
Foxp1 T C 6: 98,922,561 (GRCm39) S327G probably damaging Het
Gen1 A C 12: 11,292,297 (GRCm39) H562Q probably benign Het
Gjc2 A G 11: 59,068,386 (GRCm39) V32A probably damaging Het
Grk4 C T 5: 34,912,533 (GRCm39) H574Y probably benign Het
Kif15 T A 9: 122,804,744 (GRCm39) C93S probably damaging Het
Lrtm1 A C 14: 28,743,906 (GRCm39) I125L probably benign Het
Mrgprb8 A G 7: 48,038,527 (GRCm39) Y66C probably damaging Het
Pfn1 G A 11: 70,545,209 (GRCm39) A33V probably damaging Het
Scnn1b A C 7: 121,516,736 (GRCm39) K492Q probably damaging Het
Slc22a29 G A 19: 8,196,045 (GRCm39) probably benign Het
Spocd1 A G 4: 129,847,380 (GRCm39) D523G probably damaging Het
Tmem144 A T 3: 79,734,159 (GRCm39) D181E possibly damaging Het
Tmem220 G A 11: 66,921,933 (GRCm39) C101Y probably damaging Het
Tmpo A G 10: 90,997,741 (GRCm39) V682A probably benign Het
Wdr93 A G 7: 79,398,968 (GRCm39) K34R probably damaging Het
Zdhhc16 C A 19: 41,926,130 (GRCm39) C8* probably null Het
Zfp318 C T 17: 46,707,736 (GRCm39) R265* probably null Het
Other mutations in Cyp51
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02045:Cyp51 APN 5 4,133,247 (GRCm39) missense probably damaging 1.00
IGL02047:Cyp51 APN 5 4,149,244 (GRCm39) missense possibly damaging 0.86
IGL02492:Cyp51 APN 5 4,154,304 (GRCm39) missense probably benign 0.01
IGL03209:Cyp51 APN 5 4,154,195 (GRCm39) missense probably damaging 1.00
PIT4515001:Cyp51 UTSW 5 4,149,122 (GRCm39) critical splice donor site probably null
PIT4520001:Cyp51 UTSW 5 4,151,200 (GRCm39) missense probably damaging 1.00
R0535:Cyp51 UTSW 5 4,149,202 (GRCm39) missense probably benign 0.00
R2048:Cyp51 UTSW 5 4,136,636 (GRCm39) splice site probably benign
R2165:Cyp51 UTSW 5 4,136,594 (GRCm39) missense probably damaging 1.00
R2851:Cyp51 UTSW 5 4,149,183 (GRCm39) missense probably damaging 1.00
R3975:Cyp51 UTSW 5 4,141,877 (GRCm39) missense probably damaging 0.97
R4799:Cyp51 UTSW 5 4,133,256 (GRCm39) missense probably damaging 1.00
R5699:Cyp51 UTSW 5 4,151,213 (GRCm39) missense probably damaging 1.00
R6163:Cyp51 UTSW 5 4,150,199 (GRCm39) missense probably damaging 1.00
R6484:Cyp51 UTSW 5 4,136,627 (GRCm39) missense probably benign 0.07
R7046:Cyp51 UTSW 5 4,150,188 (GRCm39) missense probably damaging 1.00
R7155:Cyp51 UTSW 5 4,137,846 (GRCm39) missense possibly damaging 0.90
R7877:Cyp51 UTSW 5 4,152,929 (GRCm39) missense probably damaging 1.00
R7904:Cyp51 UTSW 5 4,150,173 (GRCm39) missense probably damaging 0.99
R8094:Cyp51 UTSW 5 4,136,490 (GRCm39) missense probably benign 0.08
R8095:Cyp51 UTSW 5 4,136,490 (GRCm39) missense probably benign 0.08
R8938:Cyp51 UTSW 5 4,150,202 (GRCm39) missense probably benign 0.00
R8963:Cyp51 UTSW 5 4,136,519 (GRCm39) missense probably damaging 0.98
R9097:Cyp51 UTSW 5 4,149,172 (GRCm39) missense possibly damaging 0.78
R9173:Cyp51 UTSW 5 4,136,504 (GRCm39) missense probably benign
R9416:Cyp51 UTSW 5 4,150,198 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16