Mutagenetix > Incidental Mutation

Incidental Mutation 'R7183:Cyp2j8'

559102

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

045235-MU

Accession Numbers

Essential gene?

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

Stock #

R7183 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

96444596-96507386 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 96479181 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 233 (N233K)

Ref Sequence

ENSEMBL: ENSMUSP00000134591 (fasta)

Gene Model

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

AlphaFold

G3UZ38

Predicted Effect

probably damaging
Transcript: ENSMUST00000124729
AA Change: N233K

PolyPhen 2 Score 0.967 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000134591
Gene: ENSMUSG00000082932
AA Change: N233K

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

0.9124

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (65/65)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931408C20Rik	G	A	1: 26,682,833	L1089F	probably benign	Het
Actn1	T	A	12: 80,168,932	M816L	possibly damaging	Het
Ahnak	T	C	19: 9,017,668	F5439L	probably damaging	Het
Apba2	G	A	7: 64,733,545	D369N	probably benign	Het
Arhgap32	A	G	9: 32,186,383	N228D	probably benign	Het
Arhgap33	T	A	7: 30,525,871		probably null	Het
Cacna1g	C	T	11: 94,439,737	C984Y	probably benign	Het
Cadm2	C	A	16: 66,882,832	G47*	probably null	Het
Ccdc125	A	G	13: 100,690,358	D241G	possibly damaging	Het
Ccdc39	T	G	3: 33,814,471	E822A	probably damaging	Het
Cd86	CA	CAA	16: 36,606,555		probably null	Het
Cdc42bpg	A	G	19: 6,310,797	D195G	probably damaging	Het
Cdkl1	T	C	12: 69,748,932	R275G	probably damaging	Het
Chst4	T	C	8: 110,029,998	N411S	possibly damaging	Het
Cir1	A	G	2: 73,286,386	V210A	probably damaging	Het
Col6a1	A	G	10: 76,716,259		probably null	Het
Crmp1	C	A	5: 37,288,817	H606N	probably benign	Het
Dennd1b	A	T	1: 139,170,252	Q677L	unknown	Het
Dnah17	G	A	11: 118,129,188	T11I	probably benign	Het
Ehd1	A	G	19: 6,297,654	H346R	probably benign	Het
Emc3	G	T	6: 113,531,384	Y33*	probably null	Het
Ercc5	A	T	1: 44,161,808		probably null	Het
Ercc5	G	T	1: 44,161,809		probably null	Het
Fat3	A	C	9: 15,922,837	I4153S	possibly damaging	Het
Fn3krp	T	C	11: 121,421,605		probably null	Het
Gm2035	G	A	12: 87,919,722	R46W	possibly damaging	Het
Gmnc	C	T	16: 26,960,529	D249N	probably benign	Het
Gsn	C	T	2: 35,294,948	A305V	probably benign	Het
Haus6	A	T	4: 86,583,752	H627Q	possibly damaging	Het
Heg1	A	G	16: 33,738,550		probably null	Het
Hoxd9	G	T	2: 74,698,365	V104L	possibly damaging	Het
Igkv10-96	A	C	6: 68,632,216	S32A	probably benign	Het
Kcnd2	G	A	6: 21,216,437	V47M	probably damaging	Het
Mab21l3	C	T	3: 101,815,153	V386M	probably damaging	Het
Masp2	A	G	4: 148,612,157	S404G	probably benign	Het
Olfr1024	T	A	2: 85,904,142	Q304L	probably benign	Het
Olfr1454	A	G	19: 13,064,316	I302V	probably benign	Het
Olfr835	G	T	9: 19,035,332	D70Y	probably damaging	Het
P4htm	A	T	9: 108,581,860	M291K	possibly damaging	Het
Pde6c	T	C	19: 38,133,090	S49P	probably benign	Het
Pdzd7	A	G	19: 45,037,114	V314A	probably benign	Het
Pfkl	G	A	10: 78,002,082	R31*	probably null	Het
Phlpp2	C	A	8: 109,939,953	P1038Q	probably damaging	Het
Pik3c2b	T	C	1: 133,066,465	S56P	probably benign	Het
Plec	A	G	15: 76,205,705	V145A	unknown	Het
Prg3	G	T	2: 84,993,023	D181Y	probably damaging	Het
Prg3	G	A	2: 84,991,504	V158I	probably benign	Het
Rbp3	A	G	14: 33,955,204	T370A	probably benign	Het
Rgl2	T	C	17: 33,934,990	F457L	possibly damaging	Het
Rubcnl	T	A	14: 75,049,626	M578K	probably damaging	Het
Siae	G	A	9: 37,616,946	V72M	possibly damaging	Het
Smchd1	A	T	17: 71,353,516	D1864E	probably benign	Het
Smox	T	C	2: 131,520,566	I255T	possibly damaging	Het
Tas2r123	A	G	6: 132,847,698	N186S	possibly damaging	Het
Thbs2	T	A	17: 14,690,116	I74F	possibly damaging	Het
Timm44	T	C	8: 4,267,311	D238G	probably damaging	Het
Tlk2	T	C	11: 105,221,359		probably null	Het
Tnc	A	G	4: 64,013,128	S782P	probably damaging	Het
Tpr	A	T	1: 150,406,551	K336N	probably damaging	Het
Uggt2	A	T	14: 119,019,637		probably null	Het
Vmn2r101	T	A	17: 19,612,178	I812N	probably damaging	Het
Vps33a	T	C	5: 123,535,215	Q436R	probably null	Het
Ywhaq	T	C	12: 21,416,869	K75E	possibly damaging	Het
Zfp87	A	G	13: 67,517,474	S290P	probably 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
R0718:Cyp2j8	UTSW	4	96,501,196 (GRCm38)	missense	probably benign
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
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'- CTAGGCAGCATCTTCCTCAC -3'
(R):5'- GGAGCTCTGCACATTAAAAGTG -3'

Sequencing Primer
(F):5'- CCTTTGCCATTTCTGTAAGGAAAGC -3'
(R):5'- GCTCTGCACATTAAAAGTGGCCTG -3'

Posted On

2019-06-26