Mutagenetix > Incidental Mutations

Incidental Mutation 'R1642:Cyp3a16'

173598

Institutional Source

Beutler Lab

Gene Symbol

Cyp3a16

Ensembl Gene

ENSMUSG00000038656

Gene Name

cytochrome P450, family 3, subfamily a, polypeptide 16

Synonyms

MMRRC Submission

039678-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.143) question?

Stock #

R1642 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

145436309-145469723 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 145469589 bp

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 18 (I18F)

Ref Sequence

ENSEMBL: ENSMUSP00000031633 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031633]

Predicted Effect

unknown
Transcript: ENSMUST00000031633
AA Change: I18F

SMART Domains

Protein: ENSMUSP00000031633
Gene: ENSMUSG00000038656
AA Change: I18F

Domain	Start	End	E-Value	Type
low complexity region	3	22	N/A	INTRINSIC
Pfam:p450	38	494	5.5e-132	PFAM

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.4%
20x: 89.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057J18Rik	A	G	10: 28,986,237	V19A	probably benign	Het
3632451O06Rik	T	C	14: 49,768,410		probably null	Het
4931409K22Rik	C	A	5: 24,552,688	R177L	probably damaging	Het
6820408C15Rik	T	C	2: 152,440,854	Y210H	probably damaging	Het
Aars	T	A	8: 111,043,250	I327N	possibly damaging	Het
Abca6	T	A	11: 110,218,281	N688Y	possibly damaging	Het
Ablim3	T	C	18: 61,814,311	K457R	probably benign	Het
Acsm2	A	T	7: 119,563,637	N45Y	probably damaging	Het
Agxt2	T	C	15: 10,373,831	S108P	probably damaging	Het
Akr1cl	A	T	1: 65,021,429	M174K	probably benign	Het
Bfsp1	G	A	2: 143,841,763	R214W	probably damaging	Het
Cby3	A	G	11: 50,359,516	D183G	probably damaging	Het
Clip2	T	C	5: 134,503,253	D566G	possibly damaging	Het
Colgalt1	A	G	8: 71,620,757	I341V	probably benign	Het
Cyp2c38	T	A	19: 39,401,709	D349V	probably damaging	Het
Degs2	C	T	12: 108,692,192	C176Y	probably benign	Het
Dhx16	A	T	17: 35,891,065	T995S	probably damaging	Het
Dicer1	A	T	12: 104,713,156	C521S	probably damaging	Het
Dopey2	T	C	16: 93,762,315	S532P	probably benign	Het
Dpysl4	T	G	7: 139,090,338	M124R	probably damaging	Het
Eml6	A	G	11: 29,777,001		probably null	Het
Erbb4	A	T	1: 68,331,234	V395D	probably damaging	Het
Esf1	T	C	2: 140,158,486	D460G	possibly damaging	Het
F830045P16Rik	G	A	2: 129,463,714	H247Y	probably benign	Het
Fsbp	T	A	4: 11,583,965	S221R	probably benign	Het
Fstl5	T	A	3: 76,410,622	N198K	possibly damaging	Het
Gemin5	G	T	11: 58,139,080	H855Q	probably damaging	Het
Gjd3	T	C	11: 98,982,709	E103G	probably benign	Het
I0C0044D17Rik	A	G	4: 98,820,234		probably benign	Het
Itgb4	A	T	11: 116,007,357	R1646W	probably damaging	Het
Klri2	A	T	6: 129,738,874	C121S	probably benign	Het
Lamc3	A	G	2: 31,915,996	Y703C	probably damaging	Het
Lrrc10	A	G	10: 117,045,883	N154S	probably damaging	Het
Lrriq1	A	G	10: 103,214,456	F812L	probably benign	Het
Naip2	C	T	13: 100,161,981	A516T	possibly damaging	Het
Nav1	T	C	1: 135,452,272	Y1564C	probably damaging	Het
Ndufc1	T	C	3: 51,408,243	T25A	probably benign	Het
Neurl4	A	G	11: 69,903,659	M23V	probably benign	Het
Nnt	A	G	13: 119,404,550		probably null	Het
Nolc1	G	C	19: 46,079,022		probably null	Het
Nrg1	A	T	8: 31,824,508	M289K	probably benign	Het
Oas3	G	T	5: 120,777,574	H17Q	possibly damaging	Het
Olfr1030	A	G	2: 85,983,857	K6E	probably benign	Het
Olfr239	A	G	17: 33,199,456	Y132C	probably damaging	Het
Olfr30	A	G	11: 58,455,838	I37T	probably benign	Het
Olfr957	C	T	9: 39,511,354	R122H	possibly damaging	Het
Parp9	T	C	16: 35,967,697	Y612H	probably benign	Het
Pcdh1	A	T	18: 38,199,230	M240K	possibly damaging	Het
Pcdhb9	A	G	18: 37,400,934		probably benign	Het
Plpp2	A	G	10: 79,530,684	V42A	probably damaging	Het
Ppic	C	T	18: 53,407,062	V172M	probably damaging	Het
Ppp1r9b	A	G	11: 95,001,324		silent	Het
Prop1	A	G	11: 50,953,325	V27A	possibly damaging	Het
Psmc5	A	G	11: 106,262,416	T295A	probably benign	Het
Rpa1	A	G	11: 75,312,691		probably null	Het
Rrp12	A	G	19: 41,871,737	F1016L	probably damaging	Het
Scn2a	A	T	2: 65,683,697	I242F	probably damaging	Het
Slco1a6	T	A	6: 142,086,434	H655L	probably benign	Het
Sp140	G	A	1: 85,610,824		probably null	Het
Syne1	A	G	10: 5,348,694	I1071T	possibly damaging	Het
Tbc1d9b	A	G	11: 50,149,832	D392G	probably damaging	Het
Tcaim	G	A	9: 122,818,773		probably null	Het
Tgm3	T	A	2: 130,047,782	V632E	probably damaging	Het
Triobp	C	A	15: 79,002,148	R1830S	probably damaging	Het
Ttn	A	T	2: 76,811,243	L5176Q	possibly damaging	Het
Vps8	A	G	16: 21,581,579	T1266A	probably benign	Het
Znfx1	T	C	2: 167,039,010	I285V	possibly damaging	Het

Other mutations in Cyp3a16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01386:Cyp3a16	APN	5	145440434	missense	probably damaging	0.98
IGL01964:Cyp3a16	APN	5	145455562	missense	probably benign	0.41
IGL02007:Cyp3a16	APN	5	145441948	splice site	probably benign
IGL02139:Cyp3a16	APN	5	145455480	missense	probably benign	0.10
IGL02177:Cyp3a16	APN	5	145450154	missense	probably benign	0.43
IGL02407:Cyp3a16	APN	5	145451842	missense	probably damaging	0.99
IGL02473:Cyp3a16	APN	5	145440494	missense	possibly damaging	0.54
polywog	UTSW	5	145467470	nonsense	probably null
R0363:Cyp3a16	UTSW	5	145455879	splice site	probably benign
R0556:Cyp3a16	UTSW	5	145455980	missense	probably benign	0.37
R0557:Cyp3a16	UTSW	5	145469588	missense	unknown
R0636:Cyp3a16	UTSW	5	145463085	missense	probably benign	0.03
R0749:Cyp3a16	UTSW	5	145456177	critical splice acceptor site	probably null
R0788:Cyp3a16	UTSW	5	145465076	missense	probably benign	0.00
R1552:Cyp3a16	UTSW	5	145436536	missense	probably benign	0.01
R1575:Cyp3a16	UTSW	5	145436457	missense	probably benign	0.01
R1580:Cyp3a16	UTSW	5	145442074	missense	possibly damaging	0.94
R1580:Cyp3a16	UTSW	5	145442075	missense	probably damaging	1.00
R1763:Cyp3a16	UTSW	5	145465031	critical splice donor site	probably null
R2029:Cyp3a16	UTSW	5	145451857	missense	probably damaging	0.96
R2144:Cyp3a16	UTSW	5	145456084	missense	probably damaging	1.00
R2409:Cyp3a16	UTSW	5	145440367	missense	probably benign	0.01
R2473:Cyp3a16	UTSW	5	145455594	missense	possibly damaging	0.79
R2860:Cyp3a16	UTSW	5	145455499	nonsense	probably null
R2861:Cyp3a16	UTSW	5	145455499	nonsense	probably null
R3747:Cyp3a16	UTSW	5	145442071	missense	probably damaging	1.00
R4654:Cyp3a16	UTSW	5	145436457	missense	probably benign	0.01
R4781:Cyp3a16	UTSW	5	145456112	missense	possibly damaging	0.85
R4873:Cyp3a16	UTSW	5	145452849	missense	probably benign	0.01
R4875:Cyp3a16	UTSW	5	145452849	missense	probably benign	0.01
R4925:Cyp3a16	UTSW	5	145452834	missense	probably benign	0.00
R5365:Cyp3a16	UTSW	5	145452787	missense	probably damaging	1.00
R5496:Cyp3a16	UTSW	5	145467531	missense	probably damaging	1.00
R5640:Cyp3a16	UTSW	5	145452823	missense	possibly damaging	0.94
R5761:Cyp3a16	UTSW	5	145442033	missense	possibly damaging	0.79
R6401:Cyp3a16	UTSW	5	145440364	missense	probably damaging	1.00
R6526:Cyp3a16	UTSW	5	145455895	missense	probably benign	0.01
R6528:Cyp3a16	UTSW	5	145440431	missense	probably damaging	1.00
R7000:Cyp3a16	UTSW	5	145463170	critical splice acceptor site	probably null
R7268:Cyp3a16	UTSW	5	145467470	nonsense	probably null
R7630:Cyp3a16	UTSW	5	145436310	splice site	probably null
R7938:Cyp3a16	UTSW	5	145452856	missense	probably benign	0.00
R8827:Cyp3a16	UTSW	5	145450198	missense	probably benign	0.38

Predicted Primers

PCR Primer
(F):5'- ACACACATACACTATACCATTTGCTGCC -3'
(R):5'- TGTCCAGGGAAAGAGACGACCAA -3'

Sequencing Primer
(F):5'- ggaatggagaagacagggaaag -3'
(R):5'- CAGGGGTAATCAATCTACTGGC -3'

Posted On

2014-04-24