Mutagenetix > Incidental Mutation

Incidental Mutation 'R4668:Cyp2b23'

352148

Institutional Source

Beutler Lab

Gene Symbol

Cyp2b23

Ensembl Gene

ENSMUSG00000040650

Gene Name

cytochrome P450, family 2, subfamily b, polypeptide 23

Synonyms

EG243881

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.105) question?

Stock #

R4668 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

26665227-26686437 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 26672734 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 429 (F429L)

Ref Sequence

ENSEMBL: ENSMUSP00000076578 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077356]

AlphaFold

E9Q593

Predicted Effect

probably damaging
Transcript: ENSMUST00000077356
AA Change: F429L

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000076578
Gene: ENSMUSG00000040650
AA Change: F429L

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:p450	31	488	2.9e-148	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 105 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921528I07Rik	A	T	9: 114,304,711		noncoding transcript	Het
6430548M08Rik	T	C	8: 120,160,414		probably null	Het
Abca4	G	A	3: 122,155,299	G531E	possibly damaging	Het
Acad8	A	G	9: 26,990,627	L147P	probably damaging	Het
Acot10	T	C	15: 20,665,942	S238G	probably benign	Het
Adamtsl2	A	T	2: 27,095,475	H457L	probably benign	Het
Ankrd35	A	T	3: 96,679,208	T67S	probably damaging	Het
Aox2	T	G	1: 58,334,694	I838S	possibly damaging	Het
Arnt2	T	C	7: 84,275,386	N411S	probably damaging	Het
Bmpr2	T	C	1: 59,867,716	L656S	probably damaging	Het
Carns1	A	T	19: 4,165,476	Y902*	probably null	Het
Cavin1	T	C	11: 100,958,796	E336G	probably damaging	Het
Cbl	A	T	9: 44,153,848	C728S	probably benign	Het
Ccdc136	C	A	6: 29,411,281	Q218K	probably damaging	Het
Cdk19	C	A	10: 40,466,710	T196K	probably damaging	Het
Ceacam20	T	C	7: 19,986,027	Y495H	probably damaging	Het
Celf2	T	C	2: 6,721,528	I47V	probably benign	Het
Ces3a	A	C	8: 105,053,423	K299T	probably damaging	Het
Cfap61	A	T	2: 146,143,136	I967F	probably damaging	Het
Cnksr1	C	T	4: 134,232,971		probably benign	Het
Cped1	T	C	6: 22,237,653	Y923H	probably benign	Het
Crip3	T	C	17: 46,429,364	L30P	probably damaging	Het
Csmd1	A	G	8: 16,023,891	I2030T	possibly damaging	Het
Ctse	C	A	1: 131,662,749	P70T	probably damaging	Het
Cyp2c66	T	A	19: 39,176,656	D360E	probably damaging	Het
D8Ertd738e	A	T	8: 84,249,481	L46*	probably null	Het
Dcp2	T	A	18: 44,415,362		probably null	Het
Ddx10	C	A	9: 53,099,213	D834Y	possibly damaging	Het
Ddx19a	A	T	8: 110,979,084	V245E	probably damaging	Het
Dpf2	A	C	19: 5,904,487	D130E	probably benign	Het
Emc8	A	T	8: 120,667,779	M67K	probably damaging	Het
Ephb6	T	C	6: 41,614,602	L231P	possibly damaging	Het
Erp27	T	C	6: 136,908,152	E216G	possibly damaging	Het
Esco1	A	T	18: 10,594,734	I184N	possibly damaging	Het
Fam205c	A	G	4: 42,871,608	F256L	probably benign	Het
Fdxacb1	T	A	9: 50,770,260	D11E	possibly damaging	Het
Fhod3	C	T	18: 25,066,338	P689S	probably benign	Het
Fnip1	T	A	11: 54,503,559	S940R	probably damaging	Het
Ganc	G	T	2: 120,431,067	V343F	probably benign	Het
Gldn	T	A	9: 54,332,018	L228*	probably null	Het
Gm1123	C	T	9: 99,009,373	R341H	probably damaging	Het
Gtf2f2	T	C	14: 75,917,638	Y161C	probably benign	Het
Gtf3c1	T	C	7: 125,667,338	T979A	probably damaging	Het
Hist1h4a	A	G	13: 23,760,976	V61A	probably benign	Het
Hmcn2	G	T	2: 31,435,792	R4277L	probably benign	Het
Hsd17b6	T	A	10: 127,994,426		probably null	Het
Igkv12-46	T	C	6: 69,764,797	T25A	probably damaging	Het
Inpp5e	G	A	2: 26,400,994	R354C	probably damaging	Het
Jcad	T	A	18: 4,680,221		probably null	Het
Kcna10	G	T	3: 107,194,694	A214S	possibly damaging	Het
Kit	T	C	5: 75,641,220		probably null	Het
Kmt2a	G	A	9: 44,824,572		probably benign	Het
Lama1	T	C	17: 67,752,434	V604A	probably benign	Het
Mesd	T	C	7: 83,895,756	V138A	probably damaging	Het
Mmp13	T	C	9: 7,272,580	F9S	possibly damaging	Het
Mocos	T	C	18: 24,666,434	Y242H	probably benign	Het
Mrc1	A	C	2: 14,293,486	T718P	probably damaging	Het
Msh6	T	C	17: 87,984,806	S330P	possibly damaging	Het
Myh10	A	G	11: 68,804,642	K1532E	probably damaging	Het
Nat9	T	C	11: 115,184,542	N91S	probably damaging	Het
Neto2	A	T	8: 85,641,062	I351N	probably damaging	Het
Nfx1	A	G	4: 40,976,367	N14D	possibly damaging	Het
Nlrp4b	A	G	7: 10,714,733	T288A	possibly damaging	Het
Nutm2	C	A	13: 50,472,997	T396K	probably benign	Het
Ogdhl	A	G	14: 32,332,536	T196A	probably benign	Het
Olfr1453	A	T	19: 13,028,081	F83I	probably benign	Het
Olfr548-ps1	A	G	7: 102,542,604	I223V	possibly damaging	Het
Olfr582	A	T	7: 103,041,851	D119V	probably benign	Het
Omg	T	A	11: 79,502,423	N203I	probably damaging	Het
Pdgfrb	A	G	18: 61,064,113	Y207C	probably damaging	Het
Pdzd7	T	A	19: 45,045,687		probably benign	Het
Pgs1	C	A	11: 118,003,507	H157N	probably damaging	Het
Pik3c2a	A	G	7: 116,358,688	V1121A	probably benign	Het
Pikfyve	T	A	1: 65,250,273	C1235S	probably damaging	Het
Pms1	G	A	1: 53,189,474	Q872*	probably null	Het
Ptgs2	A	G	1: 150,101,084	T23A	probably benign	Het
Rgl1	T	G	1: 152,521,371	R716S	probably damaging	Het
Rif1	A	G	2: 52,111,952	E1806G	probably benign	Het
Ripor1	T	C	8: 105,614,652	V39A	probably benign	Het
Ryr2	G	T	13: 11,593,117	T868N	probably benign	Het
Sec22b	A	T	3: 97,921,122	D167V	probably damaging	Het
Sec24d	T	C	3: 123,355,774	V810A	probably damaging	Het
Shh	T	C	5: 28,457,855	*438W	probably null	Het
Slc25a12	G	A	2: 71,315,062	S178L	probably benign	Het
Sorl1	A	T	9: 41,984,508	W1784R	probably damaging	Het
Sp3	A	T	2: 72,970,981	S229R	probably damaging	Het
Spdye4c	G	A	2: 128,592,353	V5I	possibly damaging	Het
Spint2	A	T	7: 29,260,379	V53D	probably damaging	Het
Stard3nl	T	A	13: 19,376,519	N29Y	probably damaging	Het
Stk25	A	G	1: 93,625,483	S299P	probably damaging	Het
Sult2a3	A	G	7: 14,122,861	S45P	probably damaging	Het
Thsd7a	A	T	6: 12,408,968	V685E	probably damaging	Het
Tm9sf4	T	A	2: 153,187,308	V92D	probably damaging	Het
Top2b	T	G	14: 16,409,189	I777M	probably damaging	Het
Topors	G	A	4: 40,262,669	T205I	probably damaging	Het
Tpo	T	A	12: 30,103,290	Y355F	probably benign	Het
Uba1y	T	A	Y: 826,032	M396K	possibly damaging	Het
Vmn1r50	A	T	6: 90,107,531	Q86L	probably benign	Het
Vmn1r77	A	G	7: 12,041,431	K45E	probably damaging	Het
Vmn2r114	A	C	17: 23,310,473	N218K	possibly damaging	Het
Vmn2r66	T	A	7: 84,994,697	N835I	probably damaging	Het
Vps54	T	G	11: 21,299,989	N458K	probably benign	Het
Zcchc7	G	T	4: 44,895,964	C304F	probably damaging	Het
Zfp335	A	T	2: 164,900,286	C593S	probably damaging	Het
Zmynd15	C	G	11: 70,462,588	P214R	probably damaging	Het

Other mutations in Cyp2b23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01716:Cyp2b23	APN	7	26679490	missense	probably damaging	0.98
IGL01879:Cyp2b23	APN	7	26672854	missense	probably benign	0.04
IGL02207:Cyp2b23	APN	7	26681755	missense	probably damaging	1.00
IGL03047:Cyp2b23	APN	7	26681467	splice site	probably benign
R0117:Cyp2b23	UTSW	7	26673114	missense	probably benign	0.25
R0265:Cyp2b23	UTSW	7	26672879	splice site	probably benign
R1457:Cyp2b23	UTSW	7	26673149	missense	probably damaging	1.00
R1605:Cyp2b23	UTSW	7	26686418	missense	probably benign	0.02
R1639:Cyp2b23	UTSW	7	26686417	missense	possibly damaging	0.77
R1741:Cyp2b23	UTSW	7	26673077	missense	possibly damaging	0.94
R2042:Cyp2b23	UTSW	7	26666108	missense	probably damaging	1.00
R3911:Cyp2b23	UTSW	7	26681417	missense	probably benign	0.02
R4078:Cyp2b23	UTSW	7	26673092	missense	probably damaging	1.00
R4279:Cyp2b23	UTSW	7	26666027	missense	possibly damaging	0.89
R5419:Cyp2b23	UTSW	7	26681423	nonsense	probably null
R5516:Cyp2b23	UTSW	7	26673057	nonsense	probably null
R5723:Cyp2b23	UTSW	7	26681396	missense	probably benign	0.41
R5873:Cyp2b23	UTSW	7	26675006	missense	probably benign	0.02
R6346:Cyp2b23	UTSW	7	26681725	missense	probably damaging	0.98
R6977:Cyp2b23	UTSW	7	26681320	missense	possibly damaging	0.87
R7131:Cyp2b23	UTSW	7	26681413	missense	probably benign	0.25
R7181:Cyp2b23	UTSW	7	26674403	missense	probably damaging	1.00
R7715:Cyp2b23	UTSW	7	26681695	missense	probably benign
R7877:Cyp2b23	UTSW	7	26686426	missense	probably damaging	0.97
R7880:Cyp2b23	UTSW	7	26673134	missense	probably damaging	1.00
R8004:Cyp2b23	UTSW	7	26679466	missense	probably benign
R8072:Cyp2b23	UTSW	7	26666006	missense	probably damaging	1.00
R8083:Cyp2b23	UTSW	7	26686403	missense	possibly damaging	0.62
R8968:Cyp2b23	UTSW	7	26679538	missense	probably damaging	0.99
R9129:Cyp2b23	UTSW	7	26681764	splice site	probably benign
R9437:Cyp2b23	UTSW	7	26672774	missense	possibly damaging	0.68
R9794:Cyp2b23	UTSW	7	26681696	missense	probably benign	0.14
Z1088:Cyp2b23	UTSW	7	26681411	missense	probably benign	0.06

Predicted Primers

PCR Primer
(F):5'- GGGTGCTCCTTCAGTTCAAGAC -3'
(R):5'- CACAAATCTTACCCTGTTTGTGG -3'

Sequencing Primer
(F):5'- CAGTTCAAGACTTCCCATATGGG -3'
(R):5'- CATGTGAGTCAGGGTTTGTGAACATC -3'

Posted On

2015-10-08