Mutagenetix > Incidental Mutation

Incidental Mutation 'R4471:Cyp2j12'

329416

Institutional Source

Beutler Lab

Gene Symbol

Cyp2j12

Ensembl Gene

ENSMUSG00000081225

Gene Name

cytochrome P450, family 2, subfamily j, polypeptide 12

Synonyms

OTTMUSG00000007939, Cyp2j12-ps

MMRRC Submission

041728-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R4471 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

95987555-96029389 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 96021306 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 100 (V100A)

Ref Sequence

ENSEMBL: ENSMUSP00000133811 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000097972] [ENSMUST00000121694]

AlphaFold

G3UXT0

Predicted Effect

probably benign
Transcript: ENSMUST00000097972
AA Change: V100A

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000133811
Gene: ENSMUSG00000081225
AA Change: V100A

Domain	Start	End	E-Value	Type
transmembrane domain	13	35	N/A	INTRINSIC
Pfam:p450	44	498	8.2e-139	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000121694

SMART Domains

Protein: ENSMUSP00000134394
Gene: ENSMUSG00000081225

Domain	Start	End	E-Value	Type
signal peptide	1	37	N/A	INTRINSIC
SCOP:d1cpt__	39	70	2e-8	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

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

Validation Efficiency

99% (69/70)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alpk1	A	G	3: 127,473,175 (GRCm39)	S943P	probably damaging	Het
Ankdd1a	T	C	9: 65,410,791 (GRCm39)	D398G	probably damaging	Het
Ankrd13b	T	A	11: 77,367,040 (GRCm39)	K49M	probably damaging	Het
Asah1	A	G	8: 41,796,761 (GRCm39)		probably null	Het
Cdc34b	A	G	11: 94,633,064 (GRCm39)	E88G	probably benign	Het
Cdh2	T	C	18: 16,907,533 (GRCm39)		probably null	Het
Ceacam1	T	A	7: 25,174,025 (GRCm39)	N210I	possibly damaging	Het
Celf3	A	G	3: 94,395,585 (GRCm39)		probably null	Het
Cfap20dc	A	G	14: 8,536,571 (GRCm38)	L212P	probably damaging	Het
Cmya5	A	T	13: 93,228,833 (GRCm39)	M2085K	probably benign	Het
Cpne6	G	A	14: 55,754,089 (GRCm39)	V469M	probably damaging	Het
Dnajb4	A	T	3: 151,890,799 (GRCm39)	H333Q	probably benign	Het
Eif3f	T	C	7: 108,540,153 (GRCm39)	V316A	possibly damaging	Het
Eml1	T	C	12: 108,472,894 (GRCm39)		probably benign	Het
Ern1	C	A	11: 106,310,868 (GRCm39)	V302L	possibly damaging	Het
Fam110b	A	T	4: 5,799,092 (GRCm39)	H170L	probably benign	Het
Fn3krp	T	G	11: 121,317,499 (GRCm39)	D146E	probably benign	Het
Git1	A	G	11: 77,390,650 (GRCm39)	T129A	probably benign	Het
Glrp1	T	A	1: 88,431,196 (GRCm39)	Q58L	unknown	Het
Gpatch2	A	G	1: 186,965,337 (GRCm39)	E281G	probably damaging	Het
Hipk2	T	A	6: 38,713,857 (GRCm39)		probably benign	Het
Hydin	A	G	8: 111,313,764 (GRCm39)	N4214S	probably damaging	Het
Icam5	T	A	9: 20,946,802 (GRCm39)	C443*	probably null	Het
Impdh1	G	A	6: 29,204,631 (GRCm39)	Q307*	probably null	Het
Ivns1abp	C	T	1: 151,236,990 (GRCm39)	T447M	probably benign	Het
Lman1	A	T	18: 66,124,797 (GRCm39)		probably benign	Het
Mdn1	A	G	4: 32,668,860 (GRCm39)	E306G	probably benign	Het
Msc	G	C	1: 14,825,902 (GRCm39)	P24R	probably damaging	Het
Mtif2	T	C	11: 29,490,053 (GRCm39)		probably benign	Het
Mvp	C	T	7: 126,601,130 (GRCm39)	M1I	probably null	Het
Myh7	A	T	14: 55,229,311 (GRCm39)	Y162*	probably null	Het
Nemf	G	A	12: 69,361,216 (GRCm39)	H956Y	probably benign	Het
Nktr	T	C	9: 121,577,962 (GRCm39)		probably benign	Het
Nrxn3	T	C	12: 90,171,515 (GRCm39)	S276P	probably damaging	Het
Or8d1	T	C	9: 38,766,927 (GRCm39)	S190P	probably damaging	Het
Patj	A	G	4: 98,423,816 (GRCm39)	K621E	probably damaging	Het
Prss2	A	G	6: 41,499,780 (GRCm39)	I24V	probably damaging	Het
R3hcc1l	T	C	19: 42,571,259 (GRCm39)		probably benign	Het
Rest	T	C	5: 77,429,027 (GRCm39)	V482A	probably benign	Het
Rexo1	A	T	10: 80,378,492 (GRCm39)	S476T	probably damaging	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
Slc16a3	T	C	11: 120,846,774 (GRCm39)		probably benign	Het
Slc5a4b	G	A	10: 75,894,725 (GRCm39)	Q594*	probably null	Het
Slk	T	G	19: 47,603,862 (GRCm39)	V202G	probably damaging	Het
Smarca2	T	A	19: 26,597,277 (GRCm39)	V53D	possibly damaging	Het
Snrnp200	T	A	2: 127,080,673 (GRCm39)	V2036E	probably benign	Het
Sox5	A	G	6: 143,790,491 (GRCm39)	M523T	possibly damaging	Het
Syt17	A	G	7: 118,036,040 (GRCm39)		probably null	Het
Taf2	T	C	15: 54,922,276 (GRCm39)	D337G	possibly damaging	Het
Tcstv2a	G	T	13: 120,725,579 (GRCm39)	R81L	probably benign	Het
Tecrl	A	G	5: 83,461,134 (GRCm39)	Y108H	probably benign	Het
Tln1	A	T	4: 43,551,018 (GRCm39)	F409L	probably benign	Het
Tmem59l	A	G	8: 70,939,951 (GRCm39)	L6S	unknown	Het
Ttc23	G	A	7: 67,319,904 (GRCm39)	R187Q	probably benign	Het
Ttl	T	C	2: 128,923,977 (GRCm39)	V230A	probably benign	Het
Ube2u	G	A	4: 100,338,843 (GRCm39)	W36*	probably null	Het
Ube4a	A	T	9: 44,857,830 (GRCm39)		probably benign	Het
Ulk1	C	T	5: 110,937,223 (GRCm39)	R691Q	probably benign	Het
Unc45a	A	G	7: 79,982,728 (GRCm39)	I399T	possibly damaging	Het
Utp25	C	T	1: 192,812,445 (GRCm39)	R5Q	possibly damaging	Het
Wdr59	A	C	8: 112,193,419 (GRCm39)		probably null	Het
Zfp24	A	G	18: 24,151,172 (GRCm39)		probably benign	Het
Zfp777	A	T	6: 48,019,041 (GRCm39)	W342R	probably damaging	Het
Zfp979	A	T	4: 147,697,913 (GRCm39)	C265*	probably null	Het
Zzef1	T	A	11: 72,804,157 (GRCm39)	L2633Q	probably damaging	Het

Other mutations in Cyp2j12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00580:Cyp2j12	APN	4	95,994,826 (GRCm39)	splice site	probably benign
IGL01655:Cyp2j12	APN	4	96,003,814 (GRCm39)	missense	possibly damaging	0.79
IGL01723:Cyp2j12	APN	4	95,990,363 (GRCm39)	missense	possibly damaging	0.56
IGL01737:Cyp2j12	APN	4	96,010,895 (GRCm39)	makesense	probably null
IGL01936:Cyp2j12	APN	4	96,021,306 (GRCm39)	missense	probably benign	0.01
IGL01962:Cyp2j12	APN	4	95,987,999 (GRCm39)	missense	probably benign	0.10
IGL02691:Cyp2j12	APN	4	96,021,231 (GRCm39)	critical splice donor site	probably null
R0255:Cyp2j12	UTSW	4	96,029,262 (GRCm39)	missense	probably benign	0.38
R0613:Cyp2j12	UTSW	4	95,990,316 (GRCm39)	missense	probably damaging	1.00
R0827:Cyp2j12	UTSW	4	96,001,099 (GRCm39)	splice site	probably benign
R1016:Cyp2j12	UTSW	4	96,001,102 (GRCm39)	critical splice donor site	probably null
R1251:Cyp2j12	UTSW	4	96,003,903 (GRCm39)	nonsense	probably null
R1753:Cyp2j12	UTSW	4	96,009,669 (GRCm39)	splice site	probably null
R2258:Cyp2j12	UTSW	4	96,021,315 (GRCm39)	missense	probably damaging	1.00
R4559:Cyp2j12	UTSW	4	96,001,194 (GRCm39)	missense	probably damaging	0.99
R4702:Cyp2j12	UTSW	4	96,021,230 (GRCm39)	critical splice donor site	probably null
R4923:Cyp2j12	UTSW	4	95,990,346 (GRCm39)	missense	possibly damaging	0.91
R4928:Cyp2j12	UTSW	4	95,990,388 (GRCm39)	splice site	probably null
R5591:Cyp2j12	UTSW	4	96,029,359 (GRCm39)	start gained	probably benign
R5897:Cyp2j12	UTSW	4	95,990,279 (GRCm39)	missense	probably damaging	1.00
R6176:Cyp2j12	UTSW	4	96,029,074 (GRCm39)	missense	probably damaging	0.99
R6942:Cyp2j12	UTSW	4	96,001,101 (GRCm39)	critical splice donor site	probably null
R7422:Cyp2j12	UTSW	4	96,029,222 (GRCm39)	missense	probably benign	0.05
R7453:Cyp2j12	UTSW	4	95,990,363 (GRCm39)	missense	possibly damaging	0.95
R7839:Cyp2j12	UTSW	4	95,987,893 (GRCm39)	missense	possibly damaging	0.94
R8437:Cyp2j12	UTSW	4	95,987,899 (GRCm39)	missense	probably damaging	1.00
R8445:Cyp2j12	UTSW	4	96,021,259 (GRCm39)	missense	possibly damaging	0.82
R8683:Cyp2j12	UTSW	4	96,009,805 (GRCm39)	missense	probably benign	0.41
R8701:Cyp2j12	UTSW	4	96,009,810 (GRCm39)	missense	possibly damaging	0.81
R8864:Cyp2j12	UTSW	4	96,009,750 (GRCm39)	missense	probably damaging	1.00
R8924:Cyp2j12	UTSW	4	95,994,685 (GRCm39)	missense	probably damaging	1.00
R9330:Cyp2j12	UTSW	4	95,994,791 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCTTTGACATACCATGCACATGC -3'
(R):5'- TACACCTCTAAACACTAGTCTGTC -3'

Sequencing Primer
(F):5'- CATGAAACTTTTCCAGACCTGTG -3'
(R):5'- TCTGTCTAAATACACACACACATCTG -3'

Posted On

2015-07-21