Mutagenetix > Incidental Mutations

Incidental Mutation 'R8878:Cyp2j8'

676680

Institutional Source

Beutler Lab

Gene Symbol

Cyp2j8

Ensembl Gene

ENSMUSG00000082932

Gene Name

cytochrome P450, family 2, subfamily j, polypeptide 8

Synonyms

Cyp2j8-ps, OTTMUSG00000007938

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.067) question?

Stock #

R8878 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

96444596-96507386 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 96470570 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Leucine at position 371 (V371L)

Ref Sequence

ENSEMBL: ENSMUSP00000134591 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000124729]

Predicted Effect

possibly damaging
Transcript: ENSMUST00000124729
AA Change: V371L

PolyPhen 2 Score 0.559 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000134591
Gene: ENSMUSG00000082932
AA Change: V371L

Domain	Start	End	E-Value	Type
transmembrane domain	13	35	N/A	INTRINSIC
Pfam:p450	44	500	1.2e-134	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acss2	C	A	2: 155,556,404	H348Q	probably benign	Het
Ago1	T	A	4: 126,463,723	Y53F	probably benign	Het
Arrdc5	A	G	17: 56,294,342	L261P	probably benign	Het
Asb2	C	A	12: 103,323,879	W551L	possibly damaging	Het
Atl2	T	C	17: 79,852,803	I452V	probably benign	Het
Atxn7l3	T	C	11: 102,292,719	S203G	probably benign	Het
Bche	A	G	3: 73,701,173	F307L	probably benign	Het
C6	T	C	15: 4,796,972	V679A	probably benign	Het
Cd163	A	T	6: 124,320,510	N872Y	probably damaging	Het
Cdkal1	C	A	13: 29,474,624	V380F	probably damaging	Het
Ceacam11	A	T	7: 17,975,611	I245L	probably benign	Het
Ceacam16	G	T	7: 19,858,731	T84K	possibly damaging	Het
Ceacam2	T	A	7: 25,527,926	Q172L	probably benign	Het
Chga	T	G	12: 102,561,461	S125A	possibly damaging	Het
Col9a1	T	C	1: 24,196,967		probably null	Het
Crybg3	C	A	16: 59,560,184	A236S	probably benign	Het
Csmd1	A	G	8: 15,910,528	Y3296H	probably damaging	Het
Des	C	A	1: 75,360,493	L26M	unknown	Het
Edc3	A	G	9: 57,716,201	S140G	possibly damaging	Het
Fam105a	T	A	15: 27,664,798	H24L	probably benign	Het
Fam129b	A	T	2: 32,921,093	M372L	probably benign	Het
Fam161a	C	T	11: 23,020,092	T90I	probably benign	Het
Fancm	T	C	12: 65,126,748	Y1945H	probably damaging	Het
Fbn2	C	T	18: 58,124,246	V350I	probably benign	Het
Git2	A	G	5: 114,761,588	C235R	possibly damaging	Het
Gk2	T	C	5: 97,456,482	K166E	probably benign	Het
Gm12258	G	A	11: 58,859,286	R429H	unknown	Het
Gmppa	A	G	1: 75,438,288	Y59C	probably damaging	Het
Has1	G	T	17: 17,850,059	A200E	possibly damaging	Het
Hbs1l	T	C	10: 21,358,812	I588T	possibly damaging	Het
Helz2	A	G	2: 181,232,767	V1978A	possibly damaging	Het
Hoxb9	T	C	11: 96,274,731	Y209H	probably damaging	Het
Hps5	T	C	7: 46,771,921	D706G	probably benign	Het
Hydin	T	C	8: 110,309,088	V137A	probably benign	Het
Ifngr2	T	C	16: 91,562,959	I318T	probably benign	Het
Iqgap3	C	T	3: 88,113,225	T1290I	probably damaging	Het
Jrk	A	T	15: 74,707,139	V99E	probably benign	Het
Kalrn	G	A	16: 34,198,460	P1311S	probably benign	Het
Kalrn	G	A	16: 34,205,326	T931M	probably damaging	Het
Klk9	T	C	7: 43,794,358	F99L	possibly damaging	Het
Lamb3	T	C	1: 193,330,816	C450R	probably damaging	Het
Lyst	T	A	13: 13,641,076	S1182T	probably benign	Het
Map1a	T	C	2: 121,307,644	V2933A	probably damaging	Het
Map2k5	A	T	9: 63,343,385		probably null	Het
Mcm6	A	G	1: 128,355,511		probably null	Het
Mmp17	G	A	5: 129,606,314	V505M	probably damaging	Het
Mpped2	A	G	2: 106,744,720	D50G	probably damaging	Het
Mtf1	T	A	4: 124,821,230	L216*	probably null	Het
Obscn	T	C	11: 58,999,812	E7298G	unknown	Het
Olfr39	A	G	9: 20,286,062	D129G	probably damaging	Het
Olfr598	A	T	7: 103,329,005	H173L	possibly damaging	Het
Olfr679	T	C	7: 105,086,556	L280P	probably damaging	Het
Olfr775	T	C	10: 129,251,014	L160P	probably benign	Het
Pax2	G	A	19: 44,788,776		probably null	Het
Pcnt	T	A	10: 76,408,841	E1135V	probably damaging	Het
Pgap3	A	T	11: 98,391,098	V129D	probably benign	Het
Polq	A	G	16: 37,040,507	N497S	probably benign	Het
Ppfia4	T	C	1: 134,299,384	T1138A		Het
Prickle4	A	G	17: 47,690,662	L32P		Het
Prl2c2	C	T	13: 12,997,311	G158R	probably damaging	Het
Psd3	A	G	8: 67,758,098	I752T	probably benign	Het
Sag	A	T	1: 87,828,436	Y255F	probably benign	Het
Scn7a	A	T	2: 66,675,855	D1563E	probably damaging	Het
Secisbp2	A	G	13: 51,683,368	N855S	probably benign	Het
Setd2	T	C	9: 110,592,399	V2011A	probably benign	Het
Slc30a6	T	C	17: 74,423,117	V334A	probably damaging	Het
Spen	A	G	4: 141,477,209	V1369A	unknown	Het
Stac2	T	C	11: 98,041,547	T207A	probably benign	Het
Syne2	T	C	12: 75,905,293	V445A	probably benign	Het
Tas2r131	C	A	6: 132,957,504	W114L	probably damaging	Het
Tgfbrap1	G	A	1: 43,049,799	R815*	probably null	Het
Trpv2	A	T	11: 62,590,286	I404L	probably benign	Het
Zfp236	G	A	18: 82,598,997	T1791M	probably damaging	Het

Other mutations in Cyp2j8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Cyp2j8	APN	4	96503842	missense	probably benign	0.06
IGL00418:Cyp2j8	APN	4	96444616	missense	possibly damaging	0.85
IGL01577:Cyp2j8	APN	4	96479071	missense	probably damaging	0.96
IGL01629:Cyp2j8	APN	4	96499603	missense	probably damaging	1.00
IGL01928:Cyp2j8	APN	4	96470476	splice site	probably benign
IGL01978:Cyp2j8	APN	4	96504009	splice site	probably null
IGL02053:Cyp2j8	APN	4	96470654	missense	probably damaging	1.00
IGL02500:Cyp2j8	APN	4	96470650	missense	probably damaging	1.00
IGL02947:Cyp2j8	APN	4	96470578	missense	probably damaging	1.00
cyprus	UTSW	4	96499603	missense	probably damaging	1.00
R0558:Cyp2j8	UTSW	4	96444634	missense	probably benign	0.01
R0718:Cyp2j8	UTSW	4	96501196	missense	probably benign
R1553:Cyp2j8	UTSW	4	96475557	missense	probably benign
R1557:Cyp2j8	UTSW	4	96470476	splice site	probably benign
R1632:Cyp2j8	UTSW	4	96447324	missense	probably benign	0.02
R1708:Cyp2j8	UTSW	4	96499595	missense	probably damaging	1.00
R2119:Cyp2j8	UTSW	4	96507201	missense	probably benign
R2220:Cyp2j8	UTSW	4	96444625	missense	probably benign	0.03
R3123:Cyp2j8	UTSW	4	96501213	splice site	probably benign
R3735:Cyp2j8	UTSW	4	96444599	missense	probably damaging	1.00
R3736:Cyp2j8	UTSW	4	96444599	missense	probably damaging	1.00
R4326:Cyp2j8	UTSW	4	96507329	missense	probably benign	0.10
R4327:Cyp2j8	UTSW	4	96507329	missense	probably benign	0.10
R4762:Cyp2j8	UTSW	4	96470649	missense	probably damaging	1.00
R4901:Cyp2j8	UTSW	4	96479086	missense	probably benign	0.16
R4960:Cyp2j8	UTSW	4	96507377	missense	probably benign
R5260:Cyp2j8	UTSW	4	96501064	missense	possibly damaging	0.65
R5562:Cyp2j8	UTSW	4	96470653	missense	probably damaging	1.00
R5596:Cyp2j8	UTSW	4	96507341	missense	probably benign	0.00
R5741:Cyp2j8	UTSW	4	96444643	missense	probably benign	0.00
R5825:Cyp2j8	UTSW	4	96507214	missense	probably benign	0.01
R5903:Cyp2j8	UTSW	4	96507277	missense	possibly damaging	0.46
R6122:Cyp2j8	UTSW	4	96444640	missense	probably benign
R6232:Cyp2j8	UTSW	4	96507190	missense	possibly damaging	0.94
R6748:Cyp2j8	UTSW	4	96475545	missense	probably benign	0.01
R6931:Cyp2j8	UTSW	4	96444781	splice site	probably null
R7000:Cyp2j8	UTSW	4	96447351	missense	probably benign	0.06
R7183:Cyp2j8	UTSW	4	96479181	missense	probably damaging	0.97
R7186:Cyp2j8	UTSW	4	96475550	missense	probably benign	0.00
R7348:Cyp2j8	UTSW	4	96444640	missense	probably benign	0.00
R7575:Cyp2j8	UTSW	4	96470548	missense	possibly damaging	0.63
R7648:Cyp2j8	UTSW	4	96499603	missense	probably damaging	1.00
R7975:Cyp2j8	UTSW	4	96470539	missense	possibly damaging	0.65
R7993:Cyp2j8	UTSW	4	96447219	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TCTTTTAGGCTCATTGGAGGAATAC -3'
(R):5'- TCCTTCTTTGGATGTTAGGATACAG -3'

Sequencing Primer
(F):5'- TTATTTCTTGAGGCAGAAATAGACG -3'
(R):5'- TGTTAGGATACAGAATAGCTTGACC -3'

Posted On

2021-07-15