Mutagenetix > Incidental Mutation

Incidental Mutation 'R3002:Pon2'

257273

Institutional Source

Beutler Lab

Gene Symbol

Pon2

Ensembl Gene

ENSMUSG00000032667

Gene Name

paraoxonase 2

Synonyms

6330405I24Rik

MMRRC Submission

040531-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3002 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

5264620-5298408 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 5268976 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000062670 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057792]

AlphaFold

Q62086

Predicted Effect

probably null
Transcript: ENSMUST00000057792

SMART Domains

Protein: ENSMUSP00000062670
Gene: ENSMUSG00000032667

Domain	Start	End	E-Value	Type
low complexity region	6	18	N/A	INTRINSIC
Pfam:SGL	107	303	1e-12	PFAM
Pfam:Arylesterase	167	252	3.9e-43	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123838

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135342

Meta Mutation Damage Score

0.9504

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

100% (41/41)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the paraoxonase gene family, which includes three known members located adjacent to each other on the long arm of chromosome 7. The encoded protein is ubiquitously expressed in human tissues, membrane-bound, and may act as a cellular antioxidant, protecting cells from oxidative stress. Hydrolytic activity against acylhomoserine lactones, important bacterial quorum-sensing mediators, suggests the encoded protein may also play a role in defense responses to pathogenic bacteria. Mutations in this gene may be associated with vascular disease and a number of quantitative phenotypes related to diabetes. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
PHENOTYPE: When fed an atherogenic diet, mice homozygous for a gene trapped allele show markedly lower VLDL/LDL cholesterol and serum apoB levels, higher cellular oxidative stress, enhanced macrophage immunoreactivity and LDL-induced monocyte chemotaxis, and largeratheromatous lesions than wild-type mice. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810459M11Rik	T	C	1: 85,973,802 (GRCm39)	W40R	possibly damaging	Het
A2m	A	G	6: 121,638,406 (GRCm39)	S873G	possibly damaging	Het
Acd	C	T	8: 106,426,913 (GRCm39)		probably null	Het
Acly	T	C	11: 100,395,053 (GRCm39)	K469E	possibly damaging	Het
Adcy6	T	C	15: 98,494,541 (GRCm39)	T767A	probably benign	Het
Bnip3	T	C	7: 138,496,430 (GRCm39)	I93V	probably benign	Het
Casq2	A	G	3: 102,052,517 (GRCm39)	D269G	probably damaging	Het
Ccdc180	A	G	4: 45,899,988 (GRCm39)	D182G	probably benign	Het
Cep112	A	G	11: 108,331,329 (GRCm39)	E178G	probably damaging	Het
Chrd	T	G	16: 20,556,195 (GRCm39)	Y585*	probably null	Het
Cnksr3	T	C	10: 7,102,856 (GRCm39)		probably benign	Het
Csmd1	A	G	8: 16,246,184 (GRCm39)	F1072L	probably damaging	Het
Dnai2	C	T	11: 114,641,297 (GRCm39)	P374L	probably damaging	Het
Eif4g1	T	A	16: 20,511,134 (GRCm39)	F1289I	probably damaging	Het
Eprs1	T	C	1: 185,156,588 (GRCm39)		probably null	Het
Fasn	T	C	11: 120,700,671 (GRCm39)	D2114G	probably benign	Het
Fbxl17	T	A	17: 63,532,072 (GRCm39)	E590D	probably damaging	Het
Flnb	G	T	14: 7,907,162 (GRCm38)	R1245L	probably benign	Het
Folh1	A	C	7: 86,372,519 (GRCm39)	I678M	probably damaging	Het
Frrs1l	G	T	4: 56,990,139 (GRCm39)		probably benign	Het
Hal	G	A	10: 93,343,381 (GRCm39)	A542T	probably damaging	Het
Hs3st2	T	A	7: 121,099,910 (GRCm39)	M252K	probably damaging	Het
Il27ra	G	T	8: 84,758,660 (GRCm39)	S499*	probably null	Het
Klhdc1	T	A	12: 69,302,983 (GRCm39)	V173D	possibly damaging	Het
Knop1	CTCTTCTTCTTCTTCTTCTTCTTC	CTCTTCTTCTTCTTCTTC	7: 118,451,672 (GRCm39)		probably benign	Het
Lct	T	C	1: 128,231,963 (GRCm39)	M629V	probably damaging	Het
Lnx2	A	G	5: 146,955,825 (GRCm39)	V657A	probably benign	Het
Lrig1	G	A	6: 94,585,758 (GRCm39)	S810L	probably damaging	Het
Lyst	A	T	13: 13,871,290 (GRCm39)	M2676L	probably benign	Het
Mindy4	T	A	6: 55,195,349 (GRCm39)	S188T	probably benign	Het
Mrgprb3	C	T	7: 48,293,232 (GRCm39)	M106I	probably benign	Het
Ncam1	A	G	9: 49,468,526 (GRCm39)	I311T	probably damaging	Het
Ndufa8	T	A	2: 35,926,571 (GRCm39)	E155V	possibly damaging	Het
Nr4a1	A	G	15: 101,168,853 (GRCm39)		probably null	Het
Or2a12	A	G	6: 42,904,888 (GRCm39)	H241R	probably damaging	Het
Orc3	T	C	4: 34,571,790 (GRCm39)	T660A	probably benign	Het
Otub2	T	C	12: 103,370,536 (GRCm39)	S273P	probably damaging	Het
Otulinl	T	C	15: 27,664,792 (GRCm39)	T55A	probably benign	Het
Phf11c	A	G	14: 59,622,289 (GRCm39)	L241P	probably damaging	Het
Pik3ca	T	A	3: 32,516,946 (GRCm39)	I1058N	probably damaging	Het
Pkd2l1	A	G	19: 44,143,996 (GRCm39)	F359S	possibly damaging	Het
Plxnc1	A	T	10: 94,629,080 (GRCm39)	F1565I	probably damaging	Het
Polr1a	A	G	6: 71,890,000 (GRCm39)	N73S	probably benign	Het
Polr1a	T	A	6: 71,942,628 (GRCm39)	V1156E	probably benign	Het
Ptcd1	G	A	5: 145,096,386 (GRCm39)	L236F	probably damaging	Het
Rgl2	A	G	17: 34,151,579 (GRCm39)	I208V	probably benign	Het
Rhox2e	C	A	X: 36,712,516 (GRCm39)	P69Q	probably damaging	Het
Rptor	G	A	11: 119,763,197 (GRCm39)	R927Q	possibly damaging	Het
Sec14l5	A	G	16: 4,989,746 (GRCm39)	Y230C	probably damaging	Het
Sele	G	T	1: 163,881,140 (GRCm39)	G447C	probably damaging	Het
Slc17a1	G	A	13: 24,062,564 (GRCm39)		probably null	Het
Slc2a4	A	T	11: 69,836,751 (GRCm39)	Y159*	probably null	Het
Slitrk5	A	G	14: 111,917,014 (GRCm39)	K213E	probably damaging	Het
Tdrd1	C	A	19: 56,850,182 (GRCm39)	Y981*	probably null	Het
Tex15	T	C	8: 34,064,556 (GRCm39)	Y1329H	probably benign	Het
Tgif2	C	G	2: 156,686,114 (GRCm39)	S2W	probably damaging	Het
Thoc5	A	G	11: 4,878,688 (GRCm39)	M620V	probably benign	Het
Tmeff2	C	T	1: 51,220,994 (GRCm39)	A323V	probably damaging	Het
Tmem181a	T	A	17: 6,346,061 (GRCm39)	L185H	probably damaging	Het
Tmem68	A	C	4: 3,569,588 (GRCm39)	L34W	probably damaging	Het
Tmtc4	A	T	14: 123,170,230 (GRCm39)		probably null	Het
Trpm2	A	T	10: 77,766,368 (GRCm39)		probably null	Het
Tut4	G	A	4: 108,370,125 (GRCm39)	E714K	probably damaging	Het
Tyk2	C	A	9: 21,020,617 (GRCm39)	R938L	probably benign	Het
Usp33	A	T	3: 152,063,579 (GRCm39)	T18S	probably damaging	Het
V1rd19	A	T	7: 23,703,310 (GRCm39)	I259F	probably benign	Het
Vmn2r24	A	C	6: 123,781,231 (GRCm39)	Q479P	probably benign	Het
Vmn2r98	A	G	17: 19,286,125 (GRCm39)	M208V	probably benign	Het
Wfdc6a	C	T	2: 164,422,225 (GRCm39)	V125I	probably benign	Het
Zkscan17	A	G	11: 59,378,077 (GRCm39)	C369R	probably damaging	Het

Other mutations in Pon2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01598:Pon2	APN	6	5,272,331 (GRCm39)	missense	probably damaging	1.00
IGL02683:Pon2	APN	6	5,269,062 (GRCm39)	missense	probably damaging	1.00
IGL03240:Pon2	APN	6	5,265,316 (GRCm39)	utr 3 prime	probably benign
R0102:Pon2	UTSW	6	5,289,091 (GRCm39)	splice site	probably benign
R0102:Pon2	UTSW	6	5,289,091 (GRCm39)	splice site	probably benign
R0360:Pon2	UTSW	6	5,266,156 (GRCm39)	nonsense	probably null
R0364:Pon2	UTSW	6	5,266,156 (GRCm39)	nonsense	probably null
R0402:Pon2	UTSW	6	5,272,410 (GRCm39)	nonsense	probably null
R0494:Pon2	UTSW	6	5,267,059 (GRCm39)	splice site	probably benign
R1593:Pon2	UTSW	6	5,273,003 (GRCm39)	missense	probably benign
R3001:Pon2	UTSW	6	5,268,976 (GRCm39)	critical splice donor site	probably null
R3236:Pon2	UTSW	6	5,266,986 (GRCm39)	missense	possibly damaging	0.59
R4467:Pon2	UTSW	6	5,267,021 (GRCm39)	missense	probably benign	0.24
R4911:Pon2	UTSW	6	5,269,029 (GRCm39)	missense	possibly damaging	0.93
R5237:Pon2	UTSW	6	5,265,455 (GRCm39)	missense	probably benign
R6025:Pon2	UTSW	6	5,289,057 (GRCm39)	missense	probably benign	0.40
R6313:Pon2	UTSW	6	5,272,421 (GRCm39)	missense	probably damaging	1.00
R6737:Pon2	UTSW	6	5,266,183 (GRCm39)	missense	probably benign	0.04
R7427:Pon2	UTSW	6	5,268,995 (GRCm39)	missense	probably damaging	0.99
R7438:Pon2	UTSW	6	5,289,080 (GRCm39)	missense	probably benign
R7517:Pon2	UTSW	6	5,268,997 (GRCm39)	missense	possibly damaging	0.91
R8142:Pon2	UTSW	6	5,266,239 (GRCm39)	missense	probably benign	0.01
R8318:Pon2	UTSW	6	5,265,425 (GRCm39)	missense	probably benign
R8863:Pon2	UTSW	6	5,265,480 (GRCm39)	critical splice acceptor site	probably null
R9154:Pon2	UTSW	6	5,265,391 (GRCm39)	missense	possibly damaging	0.89

Predicted Primers

PCR Primer
(F):5'- AGCCATCAACAGAGAAATGGTTAAGTC -3'
(R):5'- ATCATAGCTGTTGGGCCCAC -3'

Sequencing Primer
(F):5'- TTGAAGGAGGAATTTTAAAACCTGG -3'
(R):5'- GGCCCACCCACTTCTACG -3'

Posted On

2015-01-11