Mutagenetix > Incidental Mutation

Incidental Mutation 'R5568:Cyp2c68'

437078

Institutional Source

Beutler Lab

Gene Symbol

Cyp2c68

Ensembl Gene

ENSMUSG00000074882

Gene Name

cytochrome P450, family 2, subfamily c, polypeptide 68

Synonyms

9030012A22Rik

MMRRC Submission

043125-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5568 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

39677278-39729498 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 39677526 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 488 (I488N)

Ref Sequence

ENSEMBL: ENSMUSP00000097071 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099472]

AlphaFold

K7N6C2

Predicted Effect

probably benign
Transcript: ENSMUST00000099472
AA Change: I488N

PolyPhen 2 Score 0.189 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000097071
Gene: ENSMUSG00000074882
AA Change: I488N

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:p450	30	487	2.1e-150	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.3%
20x: 95.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 96 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4	T	C	4: 144,349,364 (GRCm39)	V207A	probably benign	Het
Abcc10	C	A	17: 46,614,834 (GRCm39)		probably null	Het
Abcc9	A	C	6: 142,634,742 (GRCm39)	V174G	possibly damaging	Het
Abl1	C	T	2: 31,669,086 (GRCm39)	A155V	probably damaging	Het
Aco2	T	A	15: 81,787,787 (GRCm39)	D212E	probably damaging	Het
Adam26b	A	T	8: 43,973,529 (GRCm39)	M491K	probably benign	Het
Anapc5	G	A	5: 122,929,988 (GRCm39)		probably benign	Het
Atf7	A	G	15: 102,471,757 (GRCm39)	I46T	probably damaging	Het
Cacna1b	A	G	2: 24,497,612 (GRCm39)	S2100P	probably damaging	Het
Capn5	T	A	7: 97,775,137 (GRCm39)	D501V	probably damaging	Het
Cc2d2a	A	G	5: 43,866,433 (GRCm39)	M748V	probably damaging	Het
Cd300c2	T	C	11: 114,891,662 (GRCm39)	T71A	probably damaging	Het
Chmp2a	T	C	7: 12,767,758 (GRCm39)	M56V	probably benign	Het
Cilp	A	C	9: 65,187,515 (GRCm39)	R1203S	probably benign	Het
Clp1	T	A	2: 84,556,322 (GRCm39)	K53*	probably null	Het
Crhbp	T	A	13: 95,578,737 (GRCm39)	D128V	probably damaging	Het
Crispld1	T	A	1: 17,820,495 (GRCm39)	I292N	probably benign	Het
Cyp3a57	A	T	5: 145,307,456 (GRCm39)	M149L	probably benign	Het
Ddx24	T	A	12: 103,390,547 (GRCm39)	Q59L	possibly damaging	Het
Ddx27	A	G	2: 166,871,439 (GRCm39)	H512R	possibly damaging	Het
Dlgap4	T	A	2: 156,604,821 (GRCm39)	*993K	probably null	Het
Dmxl2	A	T	9: 54,330,643 (GRCm39)		probably null	Het
Dus4l	A	T	12: 31,696,712 (GRCm39)	F88L	probably damaging	Het
Ep400	A	T	5: 110,904,071 (GRCm39)	V176E	probably damaging	Het
Fat3	T	A	9: 16,288,219 (GRCm39)	K435*	probably null	Het
Fsip2	T	C	2: 82,816,908 (GRCm39)	C4214R	probably benign	Het
Garin5a	T	G	7: 44,150,428 (GRCm39)	S207A	probably damaging	Het
Gfral	T	C	9: 76,072,087 (GRCm39)	*394W	probably null	Het
Glis1	T	C	4: 107,476,832 (GRCm39)	S518P	probably damaging	Het
H2-T10	A	G	17: 36,430,079 (GRCm39)		probably null	Het
Hsbp1l1	T	C	18: 80,278,679 (GRCm39)	T35A	possibly damaging	Het
Ighv5-12	A	G	12: 113,665,837 (GRCm39)	F87S	probably damaging	Het
Ints13	A	C	6: 146,477,855 (GRCm39)	D31E	probably damaging	Het
Kbtbd12	C	T	6: 88,595,609 (GRCm39)	D74N	probably damaging	Het
Klrb1c	A	G	6: 128,765,877 (GRCm39)		probably benign	Het
Kmt5b	A	T	19: 3,836,538 (GRCm39)	H25L	probably benign	Het
Krt28	A	T	11: 99,262,210 (GRCm39)	M260K	probably damaging	Het
Krt79	A	G	15: 101,838,220 (GRCm39)	S512P	probably damaging	Het
Lama1	A	T	17: 68,075,293 (GRCm39)		probably null	Het
Maneal	T	C	4: 124,750,937 (GRCm39)	E273G	possibly damaging	Het
Map4k3	T	A	17: 80,971,427 (GRCm39)	Y80F	possibly damaging	Het
Mbd6	A	G	10: 127,119,297 (GRCm39)	V946A	possibly damaging	Het
Mfsd14b	A	T	13: 65,219,936 (GRCm39)		probably null	Het
Mrpl46	C	G	7: 78,430,242 (GRCm39)	W176S	probably damaging	Het
Muc19	A	G	15: 91,768,468 (GRCm39)		noncoding transcript	Het
Mup3	T	G	4: 62,002,809 (GRCm39)	E184A	possibly damaging	Het
Myo9a	A	G	9: 59,781,911 (GRCm39)	H1699R	probably benign	Het
Ndrg2	T	A	14: 52,144,420 (GRCm39)	T269S	probably damaging	Het
Nfatc1	A	T	18: 80,693,037 (GRCm39)	V688D	probably benign	Het
Ninj2	T	C	6: 120,175,670 (GRCm39)	I101T	probably benign	Het
Nlrp10	T	A	7: 108,523,468 (GRCm39)	M671L	probably benign	Het
Npsr1	T	A	9: 24,224,510 (GRCm39)	L296I	probably damaging	Het
Or10d5	A	G	9: 39,861,983 (GRCm39)	L28P	probably benign	Het
Or52r1b	G	T	7: 102,691,517 (GRCm39)	R272L	possibly damaging	Het
Pacsin1	T	A	17: 27,927,022 (GRCm39)	D242E	probably damaging	Het
Pcdh1	T	C	18: 38,330,420 (GRCm39)	Y861C	probably damaging	Het
Pcdha12	T	C	18: 37,153,443 (GRCm39)	L54P	probably damaging	Het
Pcdhb18	T	A	18: 37,624,853 (GRCm39)	S728T	probably benign	Het
Phyhd1	T	A	2: 30,167,022 (GRCm39)	H108Q	probably damaging	Het
Plcb1	A	T	2: 135,212,513 (GRCm39)	I1035F	probably damaging	Het
Plcl1	T	C	1: 55,735,309 (GRCm39)	S217P	possibly damaging	Het
Plppr2	G	A	9: 21,852,425 (GRCm39)	R103H	probably damaging	Het
Plxnb2	G	A	15: 89,041,638 (GRCm39)	T1722I	probably damaging	Het
Pole3	T	C	4: 62,442,668 (GRCm39)	N53S	probably damaging	Het
Ptk6	A	T	2: 180,841,488 (GRCm39)	N140K	possibly damaging	Het
Rab12	C	T	17: 66,804,418 (GRCm39)	R180H	probably damaging	Het
Rab36	G	T	10: 74,888,311 (GRCm39)	V252L	probably benign	Het
Ranbp3	T	C	17: 57,008,543 (GRCm39)		probably null	Het
Rapgef2	A	G	3: 79,011,308 (GRCm39)	L259P	probably damaging	Het
Rigi	T	A	4: 40,222,140 (GRCm39)	M380L	probably benign	Het
Scaf4	GGCTGCTGCTGCTGCTGCTGCTGCTG	GGCTGCTGCTGCTGCTGCTGCTG	16: 90,026,745 (GRCm39)		probably benign	Het
Scd2	T	C	19: 44,288,142 (GRCm39)	F178S	probably damaging	Het
Shmt2	A	G	10: 127,356,250 (GRCm39)	S87P	probably damaging	Het
Slf1	T	A	13: 77,194,823 (GRCm39)	D834V	probably damaging	Het
Sorcs2	A	C	5: 36,203,874 (GRCm39)	Y540*	probably null	Het
Srpk2	T	A	5: 23,730,697 (GRCm39)	Q274L	possibly damaging	Het
Stradb	T	A	1: 59,031,901 (GRCm39)	M271K	possibly damaging	Het
Tfec	T	A	6: 16,867,592 (GRCm39)	Q16L	possibly damaging	Het
Tfg	T	C	16: 56,521,450 (GRCm39)	T63A	probably benign	Het
Ticrr	G	A	7: 79,339,715 (GRCm39)		probably null	Het
Ticrr	T	A	7: 79,345,044 (GRCm39)	C1636*	probably null	Het
Tln2	A	G	9: 67,219,147 (GRCm39)	I266T	probably damaging	Het
Tmcc1	G	C	6: 115,999,071 (GRCm39)	R323G	possibly damaging	Het
Tnnt3	A	G	7: 142,065,777 (GRCm39)	E138G	probably damaging	Het
Tpm2	C	A	4: 43,522,692 (GRCm39)	E75*	probably null	Het
Ttn	T	G	2: 76,580,922 (GRCm39)	T23324P	probably damaging	Het
Ubr4	T	G	4: 139,119,349 (GRCm39)	L176R	probably damaging	Het
Uhrf2	G	T	19: 30,016,488 (GRCm39)	D46Y	probably damaging	Het
Ulbp1	A	C	10: 7,423,281 (GRCm39)	S21A	unknown	Het
Usp17lb	C	T	7: 104,490,415 (GRCm39)	G170R	probably damaging	Het
Utp15	T	C	13: 98,394,433 (GRCm39)	N153S	probably benign	Het
Vcan	T	A	13: 89,836,790 (GRCm39)	E2918V	probably damaging	Het
Vmn1r174	T	A	7: 23,453,919 (GRCm39)	I195K	probably damaging	Het
Vmn1r76	C	T	7: 11,665,062 (GRCm39)	V16I	probably benign	Het
Xdh	T	C	17: 74,250,880 (GRCm39)	D24G	possibly damaging	Het
Xylb	T	A	9: 119,190,198 (GRCm39)	H68Q	probably benign	Het

Other mutations in Cyp2c68

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00514:Cyp2c68	APN	19	39,700,939 (GRCm39)	missense	probably damaging	0.98
IGL00826:Cyp2c68	APN	19	39,727,949 (GRCm39)	missense	possibly damaging	0.87
IGL01363:Cyp2c68	APN	19	39,691,871 (GRCm39)	missense	probably benign	0.01
IGL01892:Cyp2c68	APN	19	39,722,788 (GRCm39)	missense	probably benign	0.00
IGL02088:Cyp2c68	APN	19	39,691,965 (GRCm39)	splice site	probably benign
IGL02422:Cyp2c68	APN	19	39,722,896 (GRCm39)	missense	probably damaging	1.00
IGL03047:Cyp2c68	UTSW	19	39,722,904 (GRCm39)	missense	probably benign	0.00
R0523:Cyp2c68	UTSW	19	39,727,873 (GRCm39)	missense	probably benign	0.08
R0729:Cyp2c68	UTSW	19	39,727,994 (GRCm39)	splice site	probably benign
R0975:Cyp2c68	UTSW	19	39,691,802 (GRCm39)	missense	possibly damaging	0.85
R1117:Cyp2c68	UTSW	19	39,700,903 (GRCm39)	missense	probably damaging	1.00
R1355:Cyp2c68	UTSW	19	39,729,400 (GRCm39)	missense	probably damaging	1.00
R1370:Cyp2c68	UTSW	19	39,729,400 (GRCm39)	missense	probably damaging	1.00
R1436:Cyp2c68	UTSW	19	39,729,484 (GRCm39)	start codon destroyed	probably null	1.00
R1564:Cyp2c68	UTSW	19	39,724,024 (GRCm39)	nonsense	probably null
R1730:Cyp2c68	UTSW	19	39,687,719 (GRCm39)	missense	possibly damaging	0.87
R1865:Cyp2c68	UTSW	19	39,722,733 (GRCm39)	missense	probably benign	0.04
R1905:Cyp2c68	UTSW	19	39,724,026 (GRCm39)	missense	probably benign	0.01
R1951:Cyp2c68	UTSW	19	39,700,972 (GRCm39)	missense	probably benign	0.22
R1952:Cyp2c68	UTSW	19	39,700,972 (GRCm39)	missense	probably benign	0.22
R2224:Cyp2c68	UTSW	19	39,724,026 (GRCm39)	missense	probably benign	0.34
R2230:Cyp2c68	UTSW	19	39,687,804 (GRCm39)	missense	probably benign	0.07
R2231:Cyp2c68	UTSW	19	39,687,804 (GRCm39)	missense	probably benign	0.07
R2866:Cyp2c68	UTSW	19	39,677,589 (GRCm39)	missense	probably damaging	1.00
R3104:Cyp2c68	UTSW	19	39,722,757 (GRCm39)	missense	probably benign
R4409:Cyp2c68	UTSW	19	39,727,896 (GRCm39)	missense	probably damaging	0.98
R4575:Cyp2c68	UTSW	19	39,722,805 (GRCm39)	missense	probably benign	0.21
R4620:Cyp2c68	UTSW	19	39,701,006 (GRCm39)	splice site	probably null
R4684:Cyp2c68	UTSW	19	39,687,779 (GRCm39)	missense	possibly damaging	0.48
R5023:Cyp2c68	UTSW	19	39,700,951 (GRCm39)	missense	probably benign	0.01
R5410:Cyp2c68	UTSW	19	39,687,728 (GRCm39)	missense	possibly damaging	0.65
R5513:Cyp2c68	UTSW	19	39,691,850 (GRCm39)	missense	probably damaging	1.00
R5706:Cyp2c68	UTSW	19	39,722,762 (GRCm39)	missense	possibly damaging	0.95
R5890:Cyp2c68	UTSW	19	39,700,936 (GRCm39)	missense	probably damaging	1.00
R5897:Cyp2c68	UTSW	19	39,700,975 (GRCm39)	missense	probably benign	0.01
R6007:Cyp2c68	UTSW	19	39,722,780 (GRCm39)	missense	probably damaging	1.00
R6132:Cyp2c68	UTSW	19	39,691,858 (GRCm39)	missense	possibly damaging	0.90
R6187:Cyp2c68	UTSW	19	39,729,452 (GRCm39)	missense	probably benign	0.32
R6229:Cyp2c68	UTSW	19	39,727,622 (GRCm39)	missense	probably benign	0.02
R6341:Cyp2c68	UTSW	19	39,700,933 (GRCm39)	missense	possibly damaging	0.54
R7209:Cyp2c68	UTSW	19	39,677,649 (GRCm39)	missense	probably damaging	1.00
R7330:Cyp2c68	UTSW	19	39,677,634 (GRCm39)	missense	probably damaging	1.00
R7374:Cyp2c68	UTSW	19	39,727,648 (GRCm39)	critical splice acceptor site	probably null
R7402:Cyp2c68	UTSW	19	39,729,318 (GRCm39)	missense	probably benign	0.02
R7483:Cyp2c68	UTSW	19	39,677,581 (GRCm39)	missense	probably benign	0.02
R9103:Cyp2c68	UTSW	19	39,727,625 (GRCm39)	missense	possibly damaging	0.95
R9204:Cyp2c68	UTSW	19	39,727,571 (GRCm39)	missense	probably damaging	1.00
R9452:Cyp2c68	UTSW	19	39,687,833 (GRCm39)	missense	possibly damaging	0.75
Z1088:Cyp2c68	UTSW	19	39,727,907 (GRCm39)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- ATAGAGAACTGTTAGCCTTGGG -3'
(R):5'- GCTATTTACAAACACAGTGCCTC -3'

Sequencing Primer
(F):5'- CCTTGGGCAATTAGATAACAGAAGC -3'
(R):5'- ACAGTGCCTCTTAAACTCACTTATG -3'

Posted On

2016-10-24