Mutagenetix > Incidental Mutation

Incidental Mutation 'R0718:Cyp2j8'

63686

Institutional Source

Beutler Lab

Gene Symbol

Cyp2j8

Ensembl Gene

ENSMUSG00000082932

Gene Name

cytochrome P450, family 2, subfamily j, polypeptide 8

Synonyms

Cyp2j8-ps, OTTMUSG00000007938

MMRRC Submission

038900-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.066) question?

Stock #

R0718 (G1)

Quality Score

161

Status

Validated

Chromosome

Chromosomal Location

96444596-96507386 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 96501196 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Phenylalanine at position 130 (S130F)

Ref Sequence

ENSEMBL: ENSMUSP00000134591 (fasta)

Gene Model

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

AlphaFold

G3UZ38

Predicted Effect

probably benign
Transcript: ENSMUST00000124729
AA Change: S130F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000134591
Gene: ENSMUSG00000082932
AA Change: S130F

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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.6%
20x: 95.9%

Validation Efficiency

100% (96/96)

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamtsl4	A	T	3: 95,679,608	Y811N	possibly damaging	Het
Adrm1	T	C	2: 180,175,147		probably benign	Het
Alms1	T	A	6: 85,621,821	S1210T	probably benign	Het
Ampd3	C	T	7: 110,777,808	P11L	probably damaging	Het
Arhgap5	A	G	12: 52,516,507	E87G	possibly damaging	Het
Armc5	C	T	7: 128,240,070		probably benign	Het
Asic2	C	G	11: 80,971,456		probably benign	Het
Asph	A	G	4: 9,514,683		probably benign	Het
Bicd2	T	A	13: 49,377,875		probably null	Het
Brip1	A	G	11: 86,143,305	L530P	possibly damaging	Het
Bsn	G	T	9: 108,111,360		probably benign	Het
Btnl4	T	A	17: 34,469,634	H390L	probably benign	Het
Ccdc70	A	C	8: 21,973,308	K38T	probably damaging	Het
Ccni	G	A	5: 93,202,316	P35S	probably benign	Het
Cdh17	A	G	4: 11,810,451	D714G	possibly damaging	Het
Cenpf	A	G	1: 189,653,984	L2033P	probably damaging	Het
Cfap69	A	T	5: 5,621,924	M328K	probably damaging	Het
Cmah	T	G	13: 24,417,210		probably null	Het
Cog6	T	C	3: 53,010,629	T163A	probably benign	Het
Dgki	A	G	6: 37,012,896	V636A	probably damaging	Het
Dmkn	T	A	7: 30,764,786		probably benign	Het
Dnah6	A	G	6: 73,035,293	I3679T	possibly damaging	Het
Dsp	A	T	13: 38,196,764	Y2495F	possibly damaging	Het
Exosc4	C	T	15: 76,329,489	A171V	probably benign	Het
Fbxw24	A	G	9: 109,623,509		probably benign	Het
Flvcr1	A	T	1: 191,025,582	L171Q	probably damaging	Het
Fsd1	G	T	17: 55,996,445		probably null	Het
Gm7732	A	G	17: 21,129,844		noncoding transcript	Het
H2-K2	A	C	17: 33,975,623		noncoding transcript	Het
Hgf	A	G	5: 16,593,859	N295S	probably damaging	Het
Ift88	T	A	14: 57,517,413	D811E	probably benign	Het
Igsf9b	T	A	9: 27,323,361		probably null	Het
Immt	T	A	6: 71,863,172	V311E	probably damaging	Het
Ipo11	T	A	13: 106,919,611	N51I	possibly damaging	Het
Isy1	T	C	6: 87,819,176	K260E	probably damaging	Het
Jchain	T	G	5: 88,526,202	I28L	probably benign	Het
Jmjd1c	T	A	10: 67,218,946		probably null	Het
Kif13b	T	C	14: 64,751,662		probably benign	Het
Klhdc7b	T	C	15: 89,388,169	Y427H	possibly damaging	Het
Klhl8	T	C	5: 103,876,293		probably benign	Het
Lrp2	C	T	2: 69,510,948	D963N	probably damaging	Het
Ltbp3	G	T	19: 5,746,748		probably benign	Het
Ltf	C	A	9: 111,040,379	Q41K	probably benign	Het
Med4	T	A	14: 73,516,657	I148N	probably damaging	Het
Mlh3	T	G	12: 85,247,697	S1242R	possibly damaging	Het
Mllt6	T	C	11: 97,676,359		probably benign	Het
Mpdz	A	G	4: 81,292,473	I1712T	possibly damaging	Het
Mrgprb4	T	A	7: 48,198,553	H209L	probably benign	Het
Nkapl	A	T	13: 21,468,440	M1K	probably null	Het
Nmur2	T	A	11: 56,029,498		probably benign	Het
Nsun2	T	A	13: 69,543,697		probably benign	Het
Olfr1082	G	A	2: 86,594,081	T249I	probably benign	Het
Olfr1130	A	G	2: 87,607,927	I180V	probably benign	Het
Ovgp1	T	C	3: 105,974,830		probably benign	Het
Pcdh8	A	G	14: 79,770,691	V144A	possibly damaging	Het
Pcnx3	G	A	19: 5,677,728		probably benign	Het
Pla2r1	C	A	2: 60,479,530	V570L	possibly damaging	Het
Plxnd1	C	A	6: 115,966,638	E1202D	possibly damaging	Het
Ppp1r37	T	C	7: 19,532,254	E529G	probably benign	Het
Prdm15	A	G	16: 97,812,633	F496L	possibly damaging	Het
Prlhr	A	T	19: 60,468,005	V41D	probably benign	Het
Prlhr	G	T	19: 60,468,059	S23*	probably null	Het
Prpf4	C	T	4: 62,414,540		probably benign	Het
Psg26	T	C	7: 18,478,287	H381R	probably benign	Het
Psg26	C	T	7: 18,475,235	R416H	probably benign	Het
Ralgds	T	G	2: 28,549,116	M717R	probably benign	Het
Rbms1	T	C	2: 60,842,412	N44D	probably damaging	Het
Rpa1	T	C	11: 75,318,401		probably benign	Het
Rprd2	T	C	3: 95,766,387	N568S	probably benign	Het
Rptor	A	G	11: 119,872,376	M929V	probably benign	Het
Rspo1	T	A	4: 125,007,149	C97S	possibly damaging	Het
Scin	C	T	12: 40,079,607	G396S	probably damaging	Het
Scn9a	T	C	2: 66,547,112	N409D	probably damaging	Het
Sf3b1	A	G	1: 55,019,385	I15T	probably damaging	Het
Sh3bp2	T	C	5: 34,555,495	V149A	probably damaging	Het
Slc39a12	T	A	2: 14,407,426		probably benign	Het
Sp9	G	T	2: 73,273,827	A242S	possibly damaging	Het
Srr	A	G	11: 74,911,065	V126A	possibly damaging	Het
Tatdn3	G	T	1: 191,052,849		probably benign	Het
Tex14	G	A	11: 87,499,613	V379I	probably benign	Het
Tmed6	T	C	8: 107,061,724	N197S	probably damaging	Het
Ttbk2	G	A	2: 120,748,575	L689F	probably benign	Het
Ttbk2	A	T	2: 120,745,160	I1043N	probably benign	Het
Ttn	A	G	2: 76,810,696	S5283P	probably damaging	Het
Ube3b	C	A	5: 114,402,555	S441*	probably null	Het
Ush2a	G	A	1: 188,797,830	C3272Y	probably damaging	Het
Vac14	T	A	8: 110,632,477	I95K	probably damaging	Het
Vangl2	G	A	1: 172,006,217	A433V	probably damaging	Het
Vwa5b1	A	T	4: 138,608,824	V153D	probably damaging	Het
Zfhx3	T	A	8: 108,955,650	D3240E	unknown	Het
Zfp945	A	G	17: 22,851,030	C632R	probably damaging	Het
Zfyve26	G	A	12: 79,265,802		probably benign	Het
Zyg11b	A	T	4: 108,242,076	I606N	possibly damaging	Het

Other mutations in Cyp2j8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Cyp2j8	APN	4	96,503,842 (GRCm38)	missense	probably benign	0.06
IGL00418:Cyp2j8	APN	4	96,444,616 (GRCm38)	missense	possibly damaging	0.85
IGL01577:Cyp2j8	APN	4	96,479,071 (GRCm38)	missense	probably damaging	0.96
IGL01629:Cyp2j8	APN	4	96,499,603 (GRCm38)	missense	probably damaging	1.00
IGL01928:Cyp2j8	APN	4	96,470,476 (GRCm38)	splice site	probably benign
IGL01978:Cyp2j8	APN	4	96,504,009 (GRCm38)	splice site	probably null
IGL02053:Cyp2j8	APN	4	96,470,654 (GRCm38)	missense	probably damaging	1.00
IGL02500:Cyp2j8	APN	4	96,470,650 (GRCm38)	missense	probably damaging	1.00
IGL02947:Cyp2j8	APN	4	96,470,578 (GRCm38)	missense	probably damaging	1.00
cyprus	UTSW	4	96,499,603 (GRCm38)	missense	probably damaging	1.00
R0558:Cyp2j8	UTSW	4	96,444,634 (GRCm38)	missense	probably benign	0.01
R1553:Cyp2j8	UTSW	4	96,475,557 (GRCm38)	missense	probably benign
R1557:Cyp2j8	UTSW	4	96,470,476 (GRCm38)	splice site	probably benign
R1632:Cyp2j8	UTSW	4	96,447,324 (GRCm38)	missense	probably benign	0.02
R1708:Cyp2j8	UTSW	4	96,499,595 (GRCm38)	missense	probably damaging	1.00
R2119:Cyp2j8	UTSW	4	96,507,201 (GRCm38)	missense	probably benign
R2220:Cyp2j8	UTSW	4	96,444,625 (GRCm38)	missense	probably benign	0.03
R3123:Cyp2j8	UTSW	4	96,501,213 (GRCm38)	splice site	probably benign
R3735:Cyp2j8	UTSW	4	96,444,599 (GRCm38)	missense	probably damaging	1.00
R3736:Cyp2j8	UTSW	4	96,444,599 (GRCm38)	missense	probably damaging	1.00
R4326:Cyp2j8	UTSW	4	96,507,329 (GRCm38)	missense	probably benign	0.10
R4327:Cyp2j8	UTSW	4	96,507,329 (GRCm38)	missense	probably benign	0.10
R4762:Cyp2j8	UTSW	4	96,470,649 (GRCm38)	missense	probably damaging	1.00
R4901:Cyp2j8	UTSW	4	96,479,086 (GRCm38)	missense	probably benign	0.16
R4960:Cyp2j8	UTSW	4	96,507,377 (GRCm38)	missense	probably benign
R5260:Cyp2j8	UTSW	4	96,501,064 (GRCm38)	missense	possibly damaging	0.65
R5562:Cyp2j8	UTSW	4	96,470,653 (GRCm38)	missense	probably damaging	1.00
R5596:Cyp2j8	UTSW	4	96,507,341 (GRCm38)	missense	probably benign	0.00
R5741:Cyp2j8	UTSW	4	96,444,643 (GRCm38)	missense	probably benign	0.00
R5825:Cyp2j8	UTSW	4	96,507,214 (GRCm38)	missense	probably benign	0.01
R5903:Cyp2j8	UTSW	4	96,507,277 (GRCm38)	missense	possibly damaging	0.46
R6122:Cyp2j8	UTSW	4	96,444,640 (GRCm38)	missense	probably benign
R6232:Cyp2j8	UTSW	4	96,507,190 (GRCm38)	missense	possibly damaging	0.94
R6748:Cyp2j8	UTSW	4	96,475,545 (GRCm38)	missense	probably benign	0.01
R6931:Cyp2j8	UTSW	4	96,444,781 (GRCm38)	splice site	probably null
R7000:Cyp2j8	UTSW	4	96,447,351 (GRCm38)	missense	probably benign	0.06
R7183:Cyp2j8	UTSW	4	96,479,181 (GRCm38)	missense	probably damaging	0.97
R7186:Cyp2j8	UTSW	4	96,475,550 (GRCm38)	missense	probably benign	0.00
R7348:Cyp2j8	UTSW	4	96,444,640 (GRCm38)	missense	probably benign	0.00
R7575:Cyp2j8	UTSW	4	96,470,548 (GRCm38)	missense	possibly damaging	0.63
R7648:Cyp2j8	UTSW	4	96,499,603 (GRCm38)	missense	probably damaging	1.00
R7975:Cyp2j8	UTSW	4	96,470,539 (GRCm38)	missense	possibly damaging	0.65
R7993:Cyp2j8	UTSW	4	96,447,219 (GRCm38)	critical splice donor site	probably null
R8878:Cyp2j8	UTSW	4	96,470,570 (GRCm38)	missense	possibly damaging	0.56

Predicted Primers

PCR Primer
(F):5'- GCCTTTCCACAACCCCGTGAAATG -3'
(R):5'- AAATGTGTGCCCTGTCTTATGCTAGAG -3'

Sequencing Primer
(F):5'- CCCCGTGAAATGCCTACC -3'
(R):5'- CAGGTATGTTTCAGCTGGAATCAC -3'

Posted On

2013-07-30