Mutagenetix > Incidental Mutation

Incidental Mutation 'R1587:Cyp4a32'

177554

Institutional Source

Beutler Lab

Gene Symbol

Cyp4a32

Ensembl Gene

ENSMUSG00000063929

Gene Name

cytochrome P450, family 4, subfamily a, polypeptide 32

Synonyms

OTTMUSG00000008689

MMRRC Submission

039624-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.135) question?

Stock #

R1587 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

115458166-115478799 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 115467731 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 238 (N238K)

Ref Sequence

ENSEMBL: ENSMUSP00000081369 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084342]

AlphaFold

A2A8T1

Predicted Effect

probably benign
Transcript: ENSMUST00000084342
AA Change: N238K

PolyPhen 2 Score 0.058 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000081369
Gene: ENSMUSG00000063929
AA Change: N238K

Domain	Start	End	E-Value	Type
transmembrane domain	15	32	N/A	INTRINSIC
Pfam:p450	51	504	1.3e-133	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129918

Coding Region Coverage

1x: 99.0%
3x: 98.0%
10x: 95.2%
20x: 88.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A530064D06Rik	A	T	17: 48,473,585 (GRCm39)	S111T	probably benign	Het
Abhd2	A	T	7: 79,003,758 (GRCm39)	H279L	probably benign	Het
Ablim1	C	T	19: 57,071,979 (GRCm39)	M1I	probably null	Het
Agrn	T	C	4: 156,263,897 (GRCm39)	Q122R	probably damaging	Het
Arfgef1	A	T	1: 10,230,184 (GRCm39)	F1218I	probably damaging	Het
Bud13	C	T	9: 46,201,513 (GRCm39)	P395S	probably damaging	Het
Ccdc110	G	A	8: 46,394,783 (GRCm39)	V225M	probably benign	Het
Ccdc30	A	T	4: 119,210,373 (GRCm39)	S248T	probably damaging	Het
Cdh20	C	A	1: 110,027,757 (GRCm39)	Q501K	probably damaging	Het
Cwc27	T	C	13: 104,929,145 (GRCm39)	D266G	probably benign	Het
Cyp2d40	T	A	15: 82,645,334 (GRCm39)		probably null	Het
Ddx11	T	C	17: 66,456,251 (GRCm39)	L770P	probably damaging	Het
Dgcr8	C	T	16: 18,098,155 (GRCm39)	G412E	probably damaging	Het
Disp2	C	A	2: 118,622,064 (GRCm39)	A932D	probably damaging	Het
Dlg4	T	A	11: 69,922,572 (GRCm39)	N291K	possibly damaging	Het
Dnajc7	A	G	11: 100,492,556 (GRCm39)	I39T	probably damaging	Het
Elp1	G	A	4: 56,786,666 (GRCm39)	Q426*	probably null	Het
Eno3	T	C	11: 70,552,296 (GRCm39)	V316A	probably damaging	Het
Ep400	G	A	5: 110,874,768 (GRCm39)	T944I	probably benign	Het
Ezh2	T	G	6: 47,529,424 (GRCm39)		probably null	Het
F7	A	T	8: 13,084,783 (GRCm39)	I270F	possibly damaging	Het
Fancc	A	G	13: 63,488,246 (GRCm39)	F245L	probably benign	Het
Fzd7	G	A	1: 59,522,165 (GRCm39)	C16Y	possibly damaging	Het
Gm29394	A	G	15: 57,892,008 (GRCm39)	*200Q	probably null	Het
Ints8	A	G	4: 11,245,722 (GRCm39)		probably null	Het
Krt36	A	T	11: 99,993,128 (GRCm39)	I449N	probably damaging	Het
Ldlr	A	T	9: 21,649,209 (GRCm39)	H328L	probably damaging	Het
Limk2	T	C	11: 3,303,455 (GRCm39)	N101S	possibly damaging	Het
Lrp4	A	G	2: 91,306,650 (GRCm39)	N321S	probably benign	Het
Mafk	T	C	5: 139,785,900 (GRCm39)	S33P	probably damaging	Het
Mbtps1	T	C	8: 120,244,958 (GRCm39)	Y831C	probably damaging	Het
Mfge8	T	A	7: 78,784,513 (GRCm39)	I344F	probably damaging	Het
Myo5b	T	C	18: 74,867,061 (GRCm39)	V1430A	probably benign	Het
Nbas	G	A	12: 13,608,686 (GRCm39)	R2154H	probably benign	Het
Nlrp6	G	A	7: 140,502,959 (GRCm39)	R355H	probably damaging	Het
Noc4l	T	C	5: 110,800,889 (GRCm39)	T76A	probably benign	Het
Nrp1	T	A	8: 129,202,763 (GRCm39)	C583S	probably damaging	Het
Or2w4	C	T	13: 21,796,083 (GRCm39)	D19N	probably benign	Het
Or5d35	T	A	2: 87,855,477 (GRCm39)	M137K	probably damaging	Het
Pgm5	T	A	19: 24,793,113 (GRCm39)	I318F	probably damaging	Het
Phf1	T	A	17: 27,156,466 (GRCm39)	V536D	probably damaging	Het
Prpf4b	C	A	13: 35,076,133 (GRCm39)	A641D	probably benign	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Rbm47	A	G	5: 66,182,334 (GRCm39)	I433T	probably benign	Het
Resf1	G	T	6: 149,228,018 (GRCm39)	V355F	probably damaging	Het
S100a3	G	A	3: 90,509,618 (GRCm39)	E88K	probably benign	Het
Sesn1	A	G	10: 41,687,108 (GRCm39)	I31V	probably benign	Het
Son	T	A	16: 91,456,606 (GRCm39)	S1784R	probably damaging	Het
Srbd1	G	T	17: 86,292,865 (GRCm39)	D901E	probably damaging	Het
St8sia6	C	T	2: 13,677,416 (GRCm39)	D134N	possibly damaging	Het
Synpo2	T	A	3: 122,908,047 (GRCm39)	D423V	probably damaging	Het
Vmn2r108	A	G	17: 20,692,383 (GRCm39)	S158P	probably damaging	Het
Vmn2r109	A	T	17: 20,761,002 (GRCm39)	V785E	probably damaging	Het
Zfp143	A	G	7: 109,673,275 (GRCm39)	D124G	probably benign	Het
Zfp251	A	G	15: 76,754,484 (GRCm39)	L54P	probably damaging	Het
Zfp324	G	T	7: 12,704,570 (GRCm39)	S253I	possibly damaging	Het
Zfp59	A	G	7: 27,553,559 (GRCm39)	E337G	possibly damaging	Het
Zfp663	G	T	2: 165,195,437 (GRCm39)	Q261K	probably benign	Het
Zhx3	T	C	2: 160,623,613 (GRCm39)		probably null	Het

Other mutations in Cyp4a32

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02225:Cyp4a32	APN	4	115,467,700 (GRCm39)	missense	probably benign
IGL02546:Cyp4a32	APN	4	115,468,520 (GRCm39)	missense	probably damaging	0.98
IGL02578:Cyp4a32	APN	4	115,466,939 (GRCm39)	missense	possibly damaging	0.79
IGL02663:Cyp4a32	APN	4	115,467,787 (GRCm39)	missense	probably damaging	1.00
IGL02832:Cyp4a32	APN	4	115,471,818 (GRCm39)	missense	probably damaging	0.99
IGL03283:Cyp4a32	APN	4	115,468,280 (GRCm39)	missense	possibly damaging	0.79
IGL03357:Cyp4a32	APN	4	115,468,798 (GRCm39)	missense	probably benign	0.00
IGL03406:Cyp4a32	APN	4	115,459,500 (GRCm39)	missense	probably benign	0.00
R0379:Cyp4a32	UTSW	4	115,478,671 (GRCm39)	missense	probably damaging	1.00
R1339:Cyp4a32	UTSW	4	115,468,760 (GRCm39)	missense	probably damaging	0.98
R1435:Cyp4a32	UTSW	4	115,463,863 (GRCm39)	missense	probably damaging	0.97
R1445:Cyp4a32	UTSW	4	115,460,147 (GRCm39)	nonsense	probably null
R1520:Cyp4a32	UTSW	4	115,471,849 (GRCm39)	missense	probably damaging	0.97
R1719:Cyp4a32	UTSW	4	115,468,505 (GRCm39)	missense	possibly damaging	0.61
R1932:Cyp4a32	UTSW	4	115,468,474 (GRCm39)	missense	possibly damaging	0.78
R4184:Cyp4a32	UTSW	4	115,478,720 (GRCm39)	missense	possibly damaging	0.94
R4580:Cyp4a32	UTSW	4	115,460,126 (GRCm39)	splice site	silent
R5004:Cyp4a32	UTSW	4	115,458,238 (GRCm39)	missense	probably damaging	0.98
R6345:Cyp4a32	UTSW	4	115,459,560 (GRCm39)	missense	possibly damaging	0.81
R7231:Cyp4a32	UTSW	4	115,466,894 (GRCm39)	missense	probably damaging	1.00
R7241:Cyp4a32	UTSW	4	115,459,499 (GRCm39)	missense	probably benign
R7419:Cyp4a32	UTSW	4	115,468,234 (GRCm39)	missense	probably benign
R7716:Cyp4a32	UTSW	4	115,458,283 (GRCm39)	missense	probably damaging	1.00
R8921:Cyp4a32	UTSW	4	115,468,460 (GRCm39)	missense	probably damaging	0.99
R9009:Cyp4a32	UTSW	4	115,467,802 (GRCm39)	missense	probably null	1.00
R9266:Cyp4a32	UTSW	4	115,468,307 (GRCm39)	missense	probably damaging	1.00
R9330:Cyp4a32	UTSW	4	115,478,635 (GRCm39)	missense	probably damaging	1.00
R9345:Cyp4a32	UTSW	4	115,467,699 (GRCm39)	missense	probably benign
R9442:Cyp4a32	UTSW	4	115,468,422 (GRCm39)	missense	probably benign	0.21
Z1177:Cyp4a32	UTSW	4	115,468,542 (GRCm39)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- TGGATGCCTAGACACTCAAGCCAC -3'
(R):5'- TGTGATCCAGGTCCTAAAGGGGAG -3'

Sequencing Primer
(F):5'- taggggagtgggggtgg -3'
(R):5'- GTGCAAACAGAACCTGTGTG -3'

Posted On

2014-04-24