Mutagenetix > Incidental Mutation

Incidental Mutation 'R4816:Vmn2r105'

369853

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r105

Ensembl Gene

ENSMUSG00000091670

Gene Name

vomeronasal 2, receptor 105

Synonyms

EG627743

MMRRC Submission

042434-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4816 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

20208230-20234872 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 20208691 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 708 (I708V)

Ref Sequence

ENSEMBL: ENSMUSP00000129762 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000167382]

AlphaFold

E9Q3A5

Predicted Effect

probably benign
Transcript: ENSMUST00000167382
AA Change: I708V

PolyPhen 2 Score 0.272 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000129762
Gene: ENSMUSG00000091670
AA Change: I708V

Domain	Start	End	E-Value	Type
Pfam:ANF_receptor	85	469	6.5e-42	PFAM
Pfam:NCD3G	512	565	3.2e-21	PFAM
Pfam:7tm_3	598	833	2.5e-51	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.0%

Validation Efficiency

97% (113/116)

Allele List at MGI

Other mutations in this stock

Total: 107 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610010F05Rik	A	C	11: 23,615,243 (GRCm38)	I248S	possibly damaging	Het
8030462N17Rik	A	T	18: 77,653,299 (GRCm38)		probably null	Het
Abcc8	C	A	7: 46,104,707 (GRCm38)	A1562S	probably benign	Het
Adam30	C	A	3: 98,162,745 (GRCm38)	D631E	possibly damaging	Het
Adgrv1	T	C	13: 81,528,674 (GRCm38)	T2013A	probably damaging	Het
Als2cr12	G	A	1: 58,670,408 (GRCm38)	A196V	probably benign	Het
Baiap3	T	A	17: 25,247,295 (GRCm38)		probably benign	Het
Bicra	T	C	7: 15,988,906 (GRCm38)	T229A	possibly damaging	Het
C1qbp	A	G	11: 70,982,364 (GRCm38)		probably benign	Het
C2cd3	C	A	7: 100,391,019 (GRCm38)	T265K	probably benign	Het
Cacna1s	T	A	1: 136,115,269 (GRCm38)	I1331K	possibly damaging	Het
Cdadc1	AGACGGA	AGA	14: 59,568,991 (GRCm38)		probably null	Het
Cdcp2	A	G	4: 107,106,772 (GRCm38)	Y273C	probably damaging	Het
Cdh23	A	C	10: 60,409,077 (GRCm38)	V1013G	possibly damaging	Het
Celf3	T	A	3: 94,479,222 (GRCm38)	I39N	probably damaging	Het
Cep152	A	C	2: 125,563,754 (GRCm38)	S1619R	probably damaging	Het
Cfap36	A	G	11: 29,245,108 (GRCm38)	I42T	probably damaging	Het
Cfap61	G	T	2: 146,143,100 (GRCm38)	V955L	probably damaging	Het
Cit	G	A	5: 115,908,691 (GRCm38)	D388N	probably damaging	Het
Clca3a2	T	C	3: 144,810,852 (GRCm38)	M328V	probably benign	Het
Cntn4	A	T	6: 106,550,497 (GRCm38)	I447L	probably benign	Het
Csmd3	T	C	15: 47,857,934 (GRCm38)	T1538A	possibly damaging	Het
Cstf1	A	G	2: 172,372,985 (GRCm38)	K9E	probably damaging	Het
Dip2c	T	A	13: 9,575,150 (GRCm38)	M560K	probably benign	Het
Dsg1a	A	T	18: 20,333,722 (GRCm38)	T550S	probably benign	Het
Dtnb	A	G	12: 3,749,505 (GRCm38)	E460G	probably damaging	Het
Dus1l	GAGGTAAG	GAG	11: 120,789,758 (GRCm38)		probably benign	Het
Efl1	T	A	7: 82,671,719 (GRCm38)	V120E	probably damaging	Het
Fbxl13	T	C	5: 21,484,003 (GRCm38)	Y769C	probably benign	Het
Fcho2	T	C	13: 98,806,366 (GRCm38)	Y22C	probably damaging	Het
Gbp3	T	C	3: 142,567,574 (GRCm38)	V294A	probably damaging	Het
Gls	A	G	1: 52,199,945 (GRCm38)		probably benign	Het
Gm15130	A	T	2: 111,135,369 (GRCm38)		probably benign	Het
Gm6185	A	T	1: 161,213,158 (GRCm38)		noncoding transcript	Het
Gpr171	T	A	3: 59,098,096 (GRCm38)	H86L	probably damaging	Het
Gpr179	T	C	11: 97,339,248 (GRCm38)	T694A	probably damaging	Het
H2-Aa	A	T	17: 34,283,820 (GRCm38)	V124E	probably damaging	Het
H2-M5	A	G	17: 36,989,417 (GRCm38)		probably benign	Het
Hist1h2bl	A	G	13: 21,715,965 (GRCm38)	M60T	probably benign	Het
Igf2r	A	T	17: 12,684,097 (GRCm38)	N2355K	probably damaging	Het
Il9r	A	C	11: 32,192,654 (GRCm38)	S295A	possibly damaging	Het
Ipo9	T	C	1: 135,406,550 (GRCm38)	T313A	probably benign	Het
Kalrn	C	T	16: 34,514,019 (GRCm38)		probably benign	Het
Lama3	G	A	18: 12,477,604 (GRCm38)	V1175M	possibly damaging	Het
Lhpp	T	A	7: 132,670,375 (GRCm38)	C242*	probably null	Het
Lipe	A	G	7: 25,380,143 (GRCm38)	S1013P	probably damaging	Het
Lrrc25	C	T	8: 70,618,076 (GRCm38)	T169I	probably benign	Het
Lrrc39	T	C	3: 116,568,866 (GRCm38)		probably null	Het
Lrrd1	T	A	5: 3,851,126 (GRCm38)	L477*	probably null	Het
Lrriq4	A	G	3: 30,660,047 (GRCm38)	I515V	possibly damaging	Het
Magel2	A	G	7: 62,381,092 (GRCm38)	Y1248C	unknown	Het
Maml1	G	T	11: 50,258,335 (GRCm38)	N859K	possibly damaging	Het
Mdm1	A	T	10: 118,146,877 (GRCm38)	H139L	possibly damaging	Het
Mef2d	C	T	3: 88,168,090 (GRCm38)	P420S	possibly damaging	Het
Mgat4b	A	G	11: 50,211,021 (GRCm38)	K38E	probably benign	Het
Mtmr4	T	C	11: 87,604,097 (GRCm38)	V405A	probably damaging	Het
Naip5	G	A	13: 100,219,681 (GRCm38)	S1142F	probably benign	Het
Naip5	G	A	13: 100,219,687 (GRCm38)	T1140M	probably benign	Het
Naip5	T	C	13: 100,219,696 (GRCm38)	Q1137R	probably benign	Het
Nfe2l3	T	C	6: 51,456,624 (GRCm38)	S239P	probably damaging	Het
Nlrp3	A	G	11: 59,548,301 (GRCm38)	I235V	probably benign	Het
Nyap2	T	A	1: 81,241,313 (GRCm38)	L318Q	probably damaging	Het
Nynrin	G	A	14: 55,872,001 (GRCm38)	V1522M	probably damaging	Het
Olfr1016	A	T	2: 85,800,047 (GRCm38)	N74K	probably benign	Het
Olfr1461	A	G	19: 13,165,124 (GRCm38)	I37V	probably benign	Het
Olfr659	C	T	7: 104,670,735 (GRCm38)	P11L	probably benign	Het
Olfr810	T	C	10: 129,791,439 (GRCm38)	D50G	probably damaging	Het
Olfr875	T	A	9: 37,773,430 (GRCm38)	M257K	possibly damaging	Het
Oog3	A	G	4: 144,159,161 (GRCm38)	L289P	probably damaging	Het
Pax6	T	C	2: 105,683,784 (GRCm38)		probably benign	Het
Pbrm1	G	A	14: 31,110,448 (GRCm38)	R1441K	probably benign	Het
Pcdha9	C	T	18: 36,999,458 (GRCm38)	R527W	probably damaging	Het
Pcdhb17	T	C	18: 37,487,397 (GRCm38)	S747P	probably benign	Het
Pcnx3	A	C	19: 5,687,995 (GRCm38)		probably null	Het
Pds5a	A	T	5: 65,651,289 (GRCm38)	V413E	probably damaging	Het
Phpt1	G	T	2: 25,574,320 (GRCm38)		probably benign	Het
Phykpl	A	G	11: 51,592,953 (GRCm38)	E220G	probably benign	Het
Pias2	T	C	18: 77,105,891 (GRCm38)		probably null	Het
Pkhd1	T	A	1: 20,199,415 (GRCm38)	I3302L	probably damaging	Het
Poli	A	G	18: 70,522,751 (GRCm38)	L241P	probably damaging	Het
Ppm1h	T	A	10: 122,679,379 (GRCm38)	I65N	possibly damaging	Het
Ptpn14	T	C	1: 189,856,800 (GRCm38)	L954P	probably damaging	Het
Pxk	T	G	14: 8,136,893 (GRCm38)	M138R	probably damaging	Het
Rasl11b	G	T	5: 74,198,397 (GRCm38)	D188Y	probably damaging	Het
Rtraf	A	G	14: 19,822,576 (GRCm38)	F59S	probably benign	Het
Serpinb5	G	T	1: 106,872,339 (GRCm38)	L86F	probably damaging	Het
Setdb2	G	A	14: 59,413,646 (GRCm38)	T412I	probably benign	Het
Shank2	C	A	7: 144,052,306 (GRCm38)	N75K	probably damaging	Het
Shank3	T	A	15: 89,543,115 (GRCm38)	I791N	probably damaging	Het
Slc25a13	T	A	6: 6,114,274 (GRCm38)	M213L	possibly damaging	Het
Slc25a21	T	C	12: 56,713,838 (GRCm38)	Y298C	probably damaging	Het
Slc34a2	A	G	5: 53,069,020 (GRCm38)	N495S	probably damaging	Het
Smc2	A	G	4: 52,451,231 (GRCm38)	T292A	probably benign	Het
Spag9	T	C	11: 94,048,599 (GRCm38)		probably benign	Het
Tas2r113	C	T	6: 132,893,782 (GRCm38)	P258S	probably benign	Het
Tbkbp1	T	C	11: 97,138,741 (GRCm38)	S530G	probably benign	Het
Tenm2	A	G	11: 36,027,290 (GRCm38)	V1881A	probably damaging	Het
Tm9sf1	C	T	14: 55,641,149 (GRCm38)	R262Q	possibly damaging	Het
Tmcc3	G	T	10: 94,578,784 (GRCm38)	G147V	possibly damaging	Het
Trim38	A	T	13: 23,788,281 (GRCm38)	E195V	probably damaging	Het
Try5	T	C	6: 41,313,415 (GRCm38)	Y45C	probably benign	Het
Umad1	A	C	6: 8,457,462 (GRCm38)		probably benign	Het
Zc3h12d	A	T	10: 7,867,947 (GRCm38)	S494C	probably damaging	Het
Zeb2	A	G	2: 44,997,768 (GRCm38)	S382P	probably damaging	Het
Zfc3h1	A	G	10: 115,415,694 (GRCm38)	S1304G	probably benign	Het
Zfp287	G	T	11: 62,714,248 (GRCm38)	T611K	probably damaging	Het
Zfp534	G	A	4: 147,674,286 (GRCm38)	T642I	possibly damaging	Het

Other mutations in Vmn2r105

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01433:Vmn2r105	APN	17	20,228,555 (GRCm38)	missense	probably benign	0.01
IGL01909:Vmn2r105	APN	17	20,224,656 (GRCm38)	missense	probably damaging	1.00
IGL01925:Vmn2r105	APN	17	20,208,711 (GRCm38)	missense	possibly damaging	0.94
IGL02021:Vmn2r105	APN	17	20,227,895 (GRCm38)	missense	possibly damaging	0.49
IGL02828:Vmn2r105	APN	17	20,209,083 (GRCm38)	missense	possibly damaging	0.80
IGL02838:Vmn2r105	APN	17	20,227,585 (GRCm38)	missense	probably damaging	1.00
IGL03343:Vmn2r105	APN	17	20,226,369 (GRCm38)	nonsense	probably null
R0096:Vmn2r105	UTSW	17	20,227,479 (GRCm38)	missense	possibly damaging	0.49
R0096:Vmn2r105	UTSW	17	20,227,479 (GRCm38)	missense	possibly damaging	0.49
R0212:Vmn2r105	UTSW	17	20,208,565 (GRCm38)	missense	possibly damaging	0.90
R0268:Vmn2r105	UTSW	17	20,208,676 (GRCm38)	missense	probably benign	0.18
R0271:Vmn2r105	UTSW	17	20,234,703 (GRCm38)	missense	probably damaging	0.96
R0613:Vmn2r105	UTSW	17	20,208,316 (GRCm38)	missense	probably damaging	1.00
R0765:Vmn2r105	UTSW	17	20,227,857 (GRCm38)	missense	probably damaging	0.98
R0765:Vmn2r105	UTSW	17	20,227,711 (GRCm38)	missense	probably benign	0.20
R1162:Vmn2r105	UTSW	17	20,227,711 (GRCm38)	missense	probably benign	0.20
R1263:Vmn2r105	UTSW	17	20,208,322 (GRCm38)	missense	probably damaging	1.00
R1363:Vmn2r105	UTSW	17	20,208,670 (GRCm38)	missense	probably benign	0.00
R1464:Vmn2r105	UTSW	17	20,228,742 (GRCm38)	splice site	probably benign
R2029:Vmn2r105	UTSW	17	20,224,578 (GRCm38)	missense	probably damaging	0.99
R2420:Vmn2r105	UTSW	17	20,227,835 (GRCm38)	missense	probably benign	0.15
R2421:Vmn2r105	UTSW	17	20,227,835 (GRCm38)	missense	probably benign	0.15
R2422:Vmn2r105	UTSW	17	20,227,835 (GRCm38)	missense	probably benign	0.15
R2570:Vmn2r105	UTSW	17	20,227,323 (GRCm38)	missense	probably damaging	1.00
R3847:Vmn2r105	UTSW	17	20,208,690 (GRCm38)	missense	possibly damaging	0.85
R3848:Vmn2r105	UTSW	17	20,208,690 (GRCm38)	missense	possibly damaging	0.85
R4030:Vmn2r105	UTSW	17	20,208,754 (GRCm38)	missense	probably damaging	0.99
R4275:Vmn2r105	UTSW	17	20,228,640 (GRCm38)	missense	probably damaging	1.00
R4551:Vmn2r105	UTSW	17	20,226,351 (GRCm38)	missense	probably benign
R4801:Vmn2r105	UTSW	17	20,227,294 (GRCm38)	missense	probably benign	0.00
R4802:Vmn2r105	UTSW	17	20,227,294 (GRCm38)	missense	probably benign	0.00
R4929:Vmn2r105	UTSW	17	20,228,018 (GRCm38)	missense	probably benign	0.44
R5022:Vmn2r105	UTSW	17	20,208,414 (GRCm38)	missense	probably damaging	0.99
R5475:Vmn2r105	UTSW	17	20,234,782 (GRCm38)	missense	probably benign
R5576:Vmn2r105	UTSW	17	20,224,574 (GRCm38)	critical splice donor site	probably null
R5795:Vmn2r105	UTSW	17	20,228,736 (GRCm38)	missense	probably benign	0.00
R5895:Vmn2r105	UTSW	17	20,228,667 (GRCm38)	missense	probably benign	0.10
R6017:Vmn2r105	UTSW	17	20,208,627 (GRCm38)	missense	probably damaging	0.97
R6210:Vmn2r105	UTSW	17	20,228,496 (GRCm38)	missense	probably damaging	1.00
R6491:Vmn2r105	UTSW	17	20,227,730 (GRCm38)	nonsense	probably null
R6542:Vmn2r105	UTSW	17	20,228,541 (GRCm38)	missense	probably benign	0.03
R6729:Vmn2r105	UTSW	17	20,208,343 (GRCm38)	missense	probably damaging	0.99
R7020:Vmn2r105	UTSW	17	20,209,074 (GRCm38)	missense	probably damaging	1.00
R7033:Vmn2r105	UTSW	17	20,208,612 (GRCm38)	missense	probably damaging	0.97
R7488:Vmn2r105	UTSW	17	20,208,783 (GRCm38)	missense	probably damaging	1.00
R7491:Vmn2r105	UTSW	17	20,228,565 (GRCm38)	missense	probably benign	0.02
R7555:Vmn2r105	UTSW	17	20,227,675 (GRCm38)	missense	probably damaging	0.98
R7863:Vmn2r105	UTSW	17	20,208,675 (GRCm38)	missense	probably benign	0.18
R8137:Vmn2r105	UTSW	17	20,234,704 (GRCm38)	missense	probably benign	0.02
R8166:Vmn2r105	UTSW	17	20,208,642 (GRCm38)	missense	probably benign	0.07
R8186:Vmn2r105	UTSW	17	20,224,618 (GRCm38)	nonsense	probably null
R8214:Vmn2r105	UTSW	17	20,228,513 (GRCm38)	missense	probably benign	0.02
R8497:Vmn2r105	UTSW	17	20,234,872 (GRCm38)	start codon destroyed	probably null	0.75
R8850:Vmn2r105	UTSW	17	20,208,610 (GRCm38)	missense	probably damaging	1.00
R8880:Vmn2r105	UTSW	17	20,208,967 (GRCm38)	missense	probably damaging	0.99
R9272:Vmn2r105	UTSW	17	20,227,423 (GRCm38)	missense	probably damaging	1.00
R9506:Vmn2r105	UTSW	17	20,209,142 (GRCm38)	missense	probably benign	0.00
R9549:Vmn2r105	UTSW	17	20,227,761 (GRCm38)	missense	probably benign	0.12

Predicted Primers

PCR Primer
(F):5'- ACCAGCAAGCTGAATGACAG -3'
(R):5'- CTGCAGCAGACCACATTTG -3'

Sequencing Primer
(F):5'- TTCTAGATAAGAAGGCCACGGTG -3'
(R):5'- CACATTTGGAGTTGCATTCACTG -3'

Posted On

2016-02-04