Mutagenetix > Incidental Mutation

Incidental Mutation 'R0811:Vmn2r86'

78525

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r86

Ensembl Gene

ENSMUSG00000092162

Gene Name

vomeronasal 2, receptor 86

Synonyms

EG625109

MMRRC Submission

038991-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.071) question?

Stock #

R0811 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

130445707-130455894 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 130453628 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 133 (V133I)

Ref Sequence

ENSEMBL: ENSMUSP00000126596 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000170257]

AlphaFold

G5E8Y4

Predicted Effect

probably benign
Transcript: ENSMUST00000170257
AA Change: V133I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000126596
Gene: ENSMUSG00000092162
AA Change: V133I

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
Pfam:ANF_receptor	77	425	1.1e-25	PFAM
Pfam:NCD3G	508	562	2.4e-19	PFAM
Pfam:7tm_3	595	829	6.4e-55	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.3%
20x: 94.3%

Validation Efficiency

100% (44/44)

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930402H24Rik	A	G	2: 130,713,414	F858S	probably damaging	Het
Abcb1a	T	C	5: 8,713,229	S586P	probably damaging	Het
Ap5z1	G	A	5: 142,475,791	R583H	probably benign	Het
Arhgap28	TCAGCAGCAGCAGCAGCAGCAG	TCAGCAGCAGCAGCAGCAG	17: 67,901,299		probably benign	Het
Arrb1	G	T	7: 99,598,501	V346L	probably benign	Het
Atrnl1	T	A	19: 57,673,141	F518I	probably benign	Het
Bank1	T	A	3: 136,093,366	I405F	probably damaging	Het
Cacna1h	A	G	17: 25,388,628	L905P	probably damaging	Het
Cc2d1a	A	G	8: 84,133,836	Y826H	probably benign	Het
Cenpo	A	G	12: 4,216,643	V155A	probably benign	Het
Cnmd	A	G	14: 79,661,423	F63S	probably damaging	Het
Cnn3	G	A	3: 121,454,951	G72D	probably damaging	Het
Cox10	A	G	11: 64,071,713	S101P	probably benign	Het
Ctdsp1	T	C	1: 74,394,647	V129A	probably damaging	Het
Cyp2d34	A	T	15: 82,618,606	S140T	probably benign	Het
Dennd5a	G	A	7: 109,933,613	H317Y	possibly damaging	Het
Eef2	C	CN	10: 81,178,769		probably null	Het
Enox1	T	A	14: 77,582,436	D210E	probably damaging	Het
Fam171a1	A	G	2: 3,197,427	N190S	probably damaging	Het
Fat2	T	A	11: 55,253,633	K4138N	possibly damaging	Het
Fat4	A	T	3: 38,957,474	D2241V	probably damaging	Het
Fbn1	C	T	2: 125,403,170	V266I	possibly damaging	Het
Fras1	T	A	5: 96,752,998	S3025R	probably benign	Het
Gba	T	C	3: 89,204,000	I24T	probably benign	Het
Gdpd5	A	G	7: 99,438,333	D68G	probably damaging	Het
Grid1	G	A	14: 34,822,619	S49N	probably benign	Het
Grtp1	T	C	8: 13,179,639	T250A	possibly damaging	Het
Gucy1b1	T	C	3: 82,037,988	N448D	probably benign	Het
Hmcn2	G	A	2: 31,420,371	A3326T	probably damaging	Het
Ippk	C	A	13: 49,443,471	Q254K	probably damaging	Het
Itga2	A	T	13: 114,870,614	L393I	possibly damaging	Het
Kcna10	A	T	3: 107,195,259	E402V	possibly damaging	Het
Kcnab1	G	A	3: 65,297,720	D119N	probably damaging	Het
Kcnip4	T	A	5: 48,409,860	T122S	probably benign	Het
Kcnma1	G	A	14: 23,300,018	P1151L	probably damaging	Het
Klhl22	T	A	16: 17,792,589	M568K	probably benign	Het
Krt6a	C	T	15: 101,692,748	V257M	probably damaging	Het
Ksr2	A	C	5: 117,555,225	H246P	probably damaging	Het
Lca5	T	C	9: 83,399,753	D326G	possibly damaging	Het
Lcp1	A	G	14: 75,214,488	E393G	probably benign	Het
Leo1	G	A	9: 75,445,549	E125K	probably benign	Het
Lipt1	T	A	1: 37,875,301	V146E	probably damaging	Het
Mael	A	T	1: 166,235,399		probably null	Het
Mga	C	T	2: 119,947,961	L1996F	probably damaging	Het
Mllt6	A	G	11: 97,678,561	N913S	probably damaging	Het
Mphosph9	A	C	5: 124,298,759	D507E	probably damaging	Het
Mvp	G	A	7: 126,987,556	A801V	probably benign	Het
Neb	T	C	2: 52,292,695	D1053G	possibly damaging	Het
Nubp1	C	A	16: 10,413,721	L79I	probably benign	Het
Olfr397	G	A	11: 73,965,420	E271K	probably benign	Het
Olfr924	G	A	9: 38,848,509	V132I	probably benign	Het
Olfr97	A	C	17: 37,232,332	L13V	probably benign	Het
Pithd1	A	G	4: 135,977,134		probably benign	Het
Pnpla8	G	A	12: 44,283,405	V29M	probably benign	Het
Psmb2	T	A	4: 126,707,557	I151N	possibly damaging	Het
Ptgs2	C	T	1: 150,101,354	T104I	probably benign	Het
Ptpro	A	G	6: 137,368,079	T28A	probably benign	Het
Raf1	A	G	6: 115,626,710		probably null	Het
Ranbp2	T	C	10: 58,465,529	M668T	probably benign	Het
Rbm48	A	T	5: 3,591,760		probably null	Het
Rhag	A	T	17: 40,831,578	T225S	possibly damaging	Het
Rhof	A	C	5: 123,131,887	L69R	probably damaging	Het
Slc22a1	T	C	17: 12,666,618		probably benign	Het
Slc24a5	T	C	2: 125,068,804	S52P	probably damaging	Het
Slc8a2	T	C	7: 16,141,114	V429A	probably damaging	Het
Spam1	G	A	6: 24,796,887	R279H	probably damaging	Het
Spata16	T	A	3: 26,913,338		probably benign	Het
Srfbp1	A	G	18: 52,487,516	D102G	probably damaging	Het
Srrm3	A	C	5: 135,873,282		probably benign	Het
Tbl1xr1	T	A	3: 22,200,587		probably benign	Het
Tk1	T	C	11: 117,822,107	E98G	probably damaging	Het
Trim13	G	A	14: 61,605,700	V389I	probably benign	Het
Ttc28	A	T	5: 111,235,500	Y1289F	probably benign	Het
Ugcg	C	T	4: 59,207,798	P46S	probably benign	Het
Ugt1a10	T	A	1: 88,056,182	V234D	probably benign	Het
Vmn2r75	C	T	7: 86,165,367	G306E	probably benign	Het
Vps13c	C	A	9: 67,934,476	Q1927K	probably benign	Het
Zbtb14	C	A	17: 69,388,502	F398L	probably damaging	Het
Zfp219	T	A	14: 52,006,938	T550S	probably benign	Het
Zfp329	T	A	7: 12,811,468	N43I	probably benign	Het

Other mutations in Vmn2r86

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01295:Vmn2r86	APN	10	130453026	missense	probably damaging	0.99
IGL01328:Vmn2r86	APN	10	130452496	missense	possibly damaging	0.78
IGL01377:Vmn2r86	APN	10	130452986	missense	probably damaging	0.99
IGL01548:Vmn2r86	APN	10	130446282	missense	probably benign	0.22
IGL01804:Vmn2r86	APN	10	130452989	missense	probably damaging	0.99
IGL01921:Vmn2r86	APN	10	130455741	missense	probably benign	0.00
IGL02406:Vmn2r86	APN	10	130448639	missense	possibly damaging	0.81
IGL02625:Vmn2r86	APN	10	130452912	missense	probably damaging	1.00
IGL02960:Vmn2r86	APN	10	130453767	missense	possibly damaging	0.74
IGL03104:Vmn2r86	APN	10	130446632	missense	probably damaging	1.00
R0408:Vmn2r86	UTSW	10	130446854	missense	probably damaging	1.00
R0437:Vmn2r86	UTSW	10	130446543	missense	probably damaging	1.00
R0577:Vmn2r86	UTSW	10	130452575	missense	probably benign	0.04
R0726:Vmn2r86	UTSW	10	130446396	missense	probably damaging	1.00
R0812:Vmn2r86	UTSW	10	130453628	missense	probably benign	0.00
R1055:Vmn2r86	UTSW	10	130446357	missense	probably damaging	1.00
R1066:Vmn2r86	UTSW	10	130446276	missense	probably benign	0.01
R1199:Vmn2r86	UTSW	10	130448574	splice site	probably benign
R1332:Vmn2r86	UTSW	10	130446870	missense	probably damaging	1.00
R1568:Vmn2r86	UTSW	10	130453141	missense	probably benign	0.09
R1866:Vmn2r86	UTSW	10	130446386	missense	probably damaging	1.00
R1897:Vmn2r86	UTSW	10	130452445	missense	probably damaging	1.00
R2017:Vmn2r86	UTSW	10	130446713	missense	probably benign	0.39
R3162:Vmn2r86	UTSW	10	130455804	missense	probably damaging	0.99
R3162:Vmn2r86	UTSW	10	130455804	missense	probably damaging	0.99
R3858:Vmn2r86	UTSW	10	130455725	missense	probably benign
R4049:Vmn2r86	UTSW	10	130447097	missense	probably damaging	0.98
R4378:Vmn2r86	UTSW	10	130452600	missense	possibly damaging	0.67
R4411:Vmn2r86	UTSW	10	130452600	missense	possibly damaging	0.67
R4413:Vmn2r86	UTSW	10	130452600	missense	possibly damaging	0.67
R4422:Vmn2r86	UTSW	10	130452976	missense	possibly damaging	0.87
R4738:Vmn2r86	UTSW	10	130447070	missense	probably damaging	0.99
R4767:Vmn2r86	UTSW	10	130455737	missense	probably benign	0.00
R4872:Vmn2r86	UTSW	10	130453591	missense	probably damaging	0.98
R4880:Vmn2r86	UTSW	10	130453615	missense	probably benign	0.33
R5092:Vmn2r86	UTSW	10	130446587	missense	probably damaging	1.00
R5421:Vmn2r86	UTSW	10	130446936	missense	probably benign	0.41
R6007:Vmn2r86	UTSW	10	130453666	missense	probably damaging	1.00
R6330:Vmn2r86	UTSW	10	130446527	missense	probably benign	0.05
R6355:Vmn2r86	UTSW	10	130455894	start codon destroyed	probably damaging	0.98
R6397:Vmn2r86	UTSW	10	130446262	nonsense	probably null
R6419:Vmn2r86	UTSW	10	130446926	missense	probably damaging	1.00
R6933:Vmn2r86	UTSW	10	130446257	missense	probably damaging	1.00
R6937:Vmn2r86	UTSW	10	130448654	missense	probably damaging	1.00
R6959:Vmn2r86	UTSW	10	130446531	missense	probably damaging	1.00
R7010:Vmn2r86	UTSW	10	130455857	missense	probably benign
R7549:Vmn2r86	UTSW	10	130446828	missense	probably damaging	1.00
R8179:Vmn2r86	UTSW	10	130453084	missense	probably benign	0.00
R8257:Vmn2r86	UTSW	10	130452410	missense	possibly damaging	0.87
R8286:Vmn2r86	UTSW	10	130449986	missense	probably benign	0.03
R8479:Vmn2r86	UTSW	10	130446866	missense	probably damaging	1.00
R8805:Vmn2r86	UTSW	10	130446527	missense	probably benign	0.05
R8960:Vmn2r86	UTSW	10	130453803	missense	probably benign	0.27
R9021:Vmn2r86	UTSW	10	130447065	missense	probably damaging	1.00
R9120:Vmn2r86	UTSW	10	130453808	missense	probably benign	0.00
R9137:Vmn2r86	UTSW	10	130446540	missense	probably damaging	1.00
R9311:Vmn2r86	UTSW	10	130452571	missense	probably damaging	1.00
R9312:Vmn2r86	UTSW	10	130452537	missense	probably benign	0.02
R9433:Vmn2r86	UTSW	10	130446698	missense	possibly damaging	0.88
R9696:Vmn2r86	UTSW	10	130449833	missense	possibly damaging	0.49

Predicted Primers

PCR Primer
(F):5'- GTGTTTGGCAGCACACTCATAAATTCA -3'
(R):5'- AGGACTGTAATCTAGTTCAAGGATGGCA -3'

Sequencing Primer
(F):5'- GCACACTCATAAATTCATGCTGTC -3'
(R):5'- TCTAGTTCAAGGATGGCATTGAGAG -3'

Posted On

2013-10-16