Mutagenetix > Incidental Mutation

Incidental Mutation 'R7356:Cyp2j13'

570947

Institutional Source

Beutler Lab

Gene Symbol

Cyp2j13

Ensembl Gene

ENSMUSG00000028571

Gene Name

cytochrome P450, family 2, subfamily j, polypeptide 13

Synonyms

MMRRC Submission

045442-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R7356 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

95930897-95965803 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 95965655 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 17 (H17Q)

Ref Sequence

ENSEMBL: ENSMUSP00000030305 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030305] [ENSMUST00000097973] [ENSMUST00000107078]

AlphaFold

Q3UNV4

Predicted Effect

probably benign
Transcript: ENSMUST00000030305
AA Change: H17Q

PolyPhen 2 Score 0.226 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000030305
Gene: ENSMUSG00000028571
AA Change: H17Q

Domain	Start	End	E-Value	Type
transmembrane domain	10	32	N/A	INTRINSIC
Pfam:p450	44	499	6.7e-131	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000097973
AA Change: H17Q

PolyPhen 2 Score 0.226 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000095587
Gene: ENSMUSG00000028571
AA Change: H17Q

Domain	Start	End	E-Value	Type
transmembrane domain	10	32	N/A	INTRINSIC
Pfam:p450	44	404	8.9e-97	PFAM
low complexity region	411	420	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000107078
AA Change: H17Q

PolyPhen 2 Score 0.226 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000102693
Gene: ENSMUSG00000028571
AA Change: H17Q

Domain	Start	End	E-Value	Type
transmembrane domain	10	32	N/A	INTRINSIC
Pfam:p450	44	231	2.5e-39	PFAM
Pfam:p450	218	345	8.6e-41	PFAM
low complexity region	352	361	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acnat2	A	T	4: 49,383,507 (GRCm39)	D15E	probably damaging	Het
Adamts16	G	A	13: 70,984,399 (GRCm39)	T88I	probably benign	Het
Akap6	A	C	12: 52,958,647 (GRCm39)	N801H	probably damaging	Het
Ankfn1	G	T	11: 89,325,599 (GRCm39)	N524K	probably damaging	Het
Ap5s1	A	G	2: 131,054,582 (GRCm39)	N131S	probably damaging	Het
Astn2	A	T	4: 66,103,503 (GRCm39)	D303E	unknown	Het
Babam1	T	C	8: 71,852,208 (GRCm39)	V132A	probably benign	Het
BC028528	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	3: 95,795,448 (GRCm39)		probably benign	Het
BC028528	CACTGGTT	CACTGGTTCTATGGTGACTGGTT	3: 95,795,495 (GRCm39)		probably benign	Het
BC028528	TCTGTGGTCACTGGT	TCTGTGGTCACTGGTCCTGTGGTCACTGGT	3: 95,795,487 (GRCm39)		probably benign	Het
BC028528	GGTCACTGGTTCTGT	GGTCACTGGTTCTGTAGTCACTGGTTCTGT	3: 95,795,477 (GRCm39)		probably benign	Het
BC028528	GTTCTGTGGTCACTGGTTCTGTGGTCACTG	GTTCTGTGGTCACTGCTTCTGTGGTCACTGGTTCTGTGGTCACTG	3: 95,795,470 (GRCm39)		probably benign	Het
BC028528	TGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCAC	TGGTTCTGTGGTCACGGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCAC	3: 95,795,453 (GRCm39)		probably benign	Het
Cnst	C	T	1: 179,434,095 (GRCm39)	P304S	probably benign	Het
Cog4	A	T	8: 111,576,498 (GRCm39)		probably null	Het
Dock6	G	A	9: 21,721,195 (GRCm39)	T1662I	probably damaging	Het
Dysf	T	C	6: 84,044,443 (GRCm39)	F270S	probably damaging	Het
Erbb4	A	G	1: 68,378,514 (GRCm39)		probably null	Het
Fam120b	A	T	17: 15,627,958 (GRCm39)	Q550L	probably benign	Het
Fam83b	A	T	9: 76,400,135 (GRCm39)	F323I	probably benign	Het
Far1	T	A	7: 113,167,349 (GRCm39)	I478N	possibly damaging	Het
Gdpd5	T	A	7: 99,108,085 (GRCm39)	I554N	probably damaging	Het
Glrx3	T	C	7: 137,054,453 (GRCm39)	S79P	probably damaging	Het
Hltf	T	C	3: 20,163,534 (GRCm39)	I888T	probably damaging	Het
Hpx	A	G	7: 105,240,917 (GRCm39)	V452A	probably damaging	Het
Itk	T	G	11: 46,258,659 (GRCm39)	Q81P	possibly damaging	Het
Kdm6b	G	A	11: 69,292,991 (GRCm39)	Q1262*	probably null	Het
Lpcat2	T	C	8: 93,591,611 (GRCm39)	V85A	probably benign	Het
Lrrk2	A	T	15: 91,622,947 (GRCm39)	H1039L	probably benign	Het
Mapk3	T	C	7: 126,360,087 (GRCm39)		probably null	Het
Masp1	A	T	16: 23,288,993 (GRCm39)	N602K	possibly damaging	Het
Myo7a	T	A	7: 97,751,890 (GRCm39)	Q40L	probably benign	Het
Nek1	A	T	8: 61,573,994 (GRCm39)	M1081L	probably benign	Het
Nes	T	C	3: 87,885,058 (GRCm39)	S1106P	possibly damaging	Het
Nkpd1	A	T	7: 19,257,699 (GRCm39)	I493F	probably damaging	Het
Npsr1	C	G	9: 24,009,557 (GRCm39)	S21C	probably benign	Het
Oog1	G	A	12: 87,653,047 (GRCm39)		probably null	Het
Or11g1	G	A	14: 50,651,159 (GRCm39)	V53M	probably damaging	Het
Or5g24-ps1	G	A	2: 85,463,782 (GRCm39)	R3K	probably benign	Het
Or5k8	A	T	16: 58,644,718 (GRCm39)	M118K	probably damaging	Het
Osbpl9	G	T	4: 108,925,677 (GRCm39)	Y340*	probably null	Het
Pcyox1l	A	T	18: 61,840,621 (GRCm39)	L11Q	probably null	Het
Pdxdc1	G	A	16: 13,677,867 (GRCm39)	R255C	probably damaging	Het
Pgap1	A	G	1: 54,569,293 (GRCm39)	S358P	probably benign	Het
Pgm2l1	A	G	7: 99,917,326 (GRCm39)	Y481C	possibly damaging	Het
Plekhf1	T	C	7: 37,921,545 (GRCm39)	T8A	possibly damaging	Het
Plg	G	T	17: 12,629,798 (GRCm39)	G611C	probably damaging	Het
Prf1	A	C	10: 61,139,059 (GRCm39)	D339A	possibly damaging	Het
Prph	A	G	15: 98,954,807 (GRCm39)	Y291C	probably damaging	Het
Rasal1	A	G	5: 120,792,890 (GRCm39)	S48G	possibly damaging	Het
Rigi	A	G	4: 40,226,600 (GRCm39)	S231P	probably benign	Het
Ripk4	T	A	16: 97,544,349 (GRCm39)	Q766L	probably damaging	Het
Scaf1	T	C	7: 44,657,208 (GRCm39)	D557G	unknown	Het
Scaper	A	T	9: 55,799,495 (GRCm39)	M190K	unknown	Het
Scn8a	A	T	15: 100,855,460 (GRCm39)	I202F	probably damaging	Het
Siglecf	A	G	7: 43,005,855 (GRCm39)	I505V	probably benign	Het
Sirpb1c	A	G	3: 15,886,297 (GRCm39)	S360P	probably benign	Het
Sla2	C	A	2: 156,720,623 (GRCm39)		probably null	Het
Slc11a1	G	T	1: 74,424,648 (GRCm39)	V544L	probably benign	Het
Slco1a5	T	A	6: 142,180,458 (GRCm39)	K648I	probably benign	Het
Sorcs1	T	A	19: 50,163,595 (GRCm39)	I1020F	possibly damaging	Het
Spen	C	A	4: 141,199,235 (GRCm39)	E3131*	probably null	Het
Sult2a7	A	T	7: 14,211,031 (GRCm39)	W162R	probably damaging	Het
Sult3a1	G	A	10: 33,742,579 (GRCm39)	E69K	probably benign	Het
Tcof1	G	T	18: 60,951,166 (GRCm39)	D1119E	unknown	Het
Tom1l2	A	T	11: 60,139,853 (GRCm39)	I272K	probably damaging	Het
Tspan5	C	T	3: 138,448,193 (GRCm39)		probably benign	Het
Ttn	A	G	2: 76,698,244 (GRCm39)	L186P		Het
Uap1l1	T	C	2: 25,251,696 (GRCm39)	E496G	possibly damaging	Het
Ube2v1	A	T	2: 167,451,115 (GRCm39)	I117N	possibly damaging	Het
Usp42	A	G	5: 143,702,842 (GRCm39)	V593A	possibly damaging	Het
Virma	T	A	4: 11,513,595 (GRCm39)	I483N	probably damaging	Het
Vwde	T	A	6: 13,192,641 (GRCm39)	I421F	probably damaging	Het
Zfp345	G	A	2: 150,314,209 (GRCm39)	H443Y	probably damaging	Het
Zfp760	A	G	17: 21,941,601 (GRCm39)	T259A	probably benign	Het
Zfp941	T	C	7: 140,392,028 (GRCm39)	I444V	possibly damaging	Het
Zfyve9	A	C	4: 108,576,212 (GRCm39)	S290A	probably benign	Het

Other mutations in Cyp2j13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00470:Cyp2j13	APN	4	95,950,275 (GRCm39)	missense	probably damaging	1.00
IGL01511:Cyp2j13	APN	4	95,965,552 (GRCm39)	missense	possibly damaging	0.79
IGL01540:Cyp2j13	APN	4	95,956,959 (GRCm39)	splice site	probably benign
IGL01923:Cyp2j13	APN	4	95,950,294 (GRCm39)	missense	probably benign	0.00
IGL03124:Cyp2j13	APN	4	95,950,159 (GRCm39)	missense	possibly damaging	0.78
IGL03389:Cyp2j13	APN	4	95,956,558 (GRCm39)	missense	probably damaging	1.00
R0671:Cyp2j13	UTSW	4	95,959,932 (GRCm39)	missense	probably damaging	0.97
R1351:Cyp2j13	UTSW	4	95,945,155 (GRCm39)	missense	probably benign	0.00
R1510:Cyp2j13	UTSW	4	95,950,209 (GRCm39)	missense	possibly damaging	0.48
R1708:Cyp2j13	UTSW	4	95,950,304 (GRCm39)	missense	probably damaging	0.99
R2327:Cyp2j13	UTSW	4	95,947,344 (GRCm39)	missense	possibly damaging	0.50
R3834:Cyp2j13	UTSW	4	95,944,794 (GRCm39)	critical splice donor site	probably null
R4643:Cyp2j13	UTSW	4	95,945,161 (GRCm39)	missense	possibly damaging	0.62
R4867:Cyp2j13	UTSW	4	95,947,235 (GRCm39)	missense	possibly damaging	0.68
R4900:Cyp2j13	UTSW	4	95,947,280 (GRCm39)	missense	probably damaging	1.00
R5175:Cyp2j13	UTSW	4	95,956,452 (GRCm39)	missense	possibly damaging	0.55
R5291:Cyp2j13	UTSW	4	95,956,566 (GRCm39)	missense	probably damaging	1.00
R5770:Cyp2j13	UTSW	4	95,965,669 (GRCm39)	missense	probably benign	0.23
R5837:Cyp2j13	UTSW	4	95,959,919 (GRCm39)	missense	probably damaging	0.98
R5912:Cyp2j13	UTSW	4	95,945,079 (GRCm39)	missense	probably damaging	1.00
R6283:Cyp2j13	UTSW	4	95,945,074 (GRCm39)	missense	possibly damaging	0.89
R6362:Cyp2j13	UTSW	4	95,959,932 (GRCm39)	missense	probably damaging	0.97
R6627:Cyp2j13	UTSW	4	95,947,343 (GRCm39)	missense	probably damaging	0.96
R7001:Cyp2j13	UTSW	4	95,945,112 (GRCm39)	missense	probably damaging	1.00
R7620:Cyp2j13	UTSW	4	95,944,899 (GRCm39)	missense	probably benign	0.25
R8717:Cyp2j13	UTSW	4	95,933,777 (GRCm39)	missense	probably benign	0.06
R8810:Cyp2j13	UTSW	4	95,945,153 (GRCm39)	missense	probably benign	0.30
R8850:Cyp2j13	UTSW	4	95,956,428 (GRCm39)	missense	probably benign	0.09
R8981:Cyp2j13	UTSW	4	95,965,527 (GRCm39)	missense	possibly damaging	0.87
R9359:Cyp2j13	UTSW	4	95,950,170 (GRCm39)	missense	probably damaging	1.00
R9595:Cyp2j13	UTSW	4	95,933,797 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- ATCAGGGCAAATCCAGGCAC -3'
(R):5'- TCTCAGGGCCTTAAGAGAAAATGG -3'

Sequencing Primer
(F):5'- GGCAAATCCAGGCACTCTCTC -3'
(R):5'- ATGGAAGGGCGTGGCTG -3'

Posted On

2019-09-13