Mutagenetix > Incidental Mutation

Incidental Mutation 'R5124:Vmn1r202'

393464

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r202

Ensembl Gene

ENSMUSG00000094379

Gene Name

vomeronasal 1 receptor 202

Synonyms

V1ri7

MMRRC Submission

042712-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.087) question?

Stock #

R5124 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

22685507-22686415 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 22685920 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 166 (V166I)

Ref Sequence

ENSEMBL: ENSMUSP00000154314 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078642] [ENSMUST00000228020]

AlphaFold

Q8R259

Predicted Effect

probably benign
Transcript: ENSMUST00000078642
AA Change: V166I

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)

SMART Domains

Protein: ENSMUSP00000077711
Gene: ENSMUSG00000094379
AA Change: V166I

Domain	Start	End	E-Value	Type
Pfam:TAS2R	5	301	2.2e-11	PFAM
Pfam:V1R	35	300	5.6e-44	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000228020
AA Change: V166I

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.6%
20x: 93.5%

Validation Efficiency

100% (60/60)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4fm4	A	T	4: 144,401,289 (GRCm39)	I65N	probably damaging	Het
Adpgk	A	G	9: 59,222,561 (GRCm39)	D496G	possibly damaging	Het
Agbl4	A	G	4: 111,513,525 (GRCm39)	M424V	probably benign	Het
Akap10	C	T	11: 61,807,015 (GRCm39)	A72T	probably damaging	Het
Bpifa3	C	T	2: 153,980,057 (GRCm39)	Q230*	probably null	Het
Cog4	G	T	8: 111,573,825 (GRCm39)	R48L	probably damaging	Het
Cop1	A	G	1: 159,105,682 (GRCm39)	Y33C	probably damaging	Het
Cyp26a1	A	T	19: 37,689,665 (GRCm39)	I454L	probably benign	Het
Ddr1	T	C	17: 35,994,489 (GRCm39)	H762R	probably damaging	Het
Dnajc2	A	T	5: 21,968,482 (GRCm39)	S328T	probably benign	Het
Dppa2	G	T	16: 48,131,986 (GRCm39)	V28F	probably damaging	Het
Dusp15	T	A	2: 152,793,275 (GRCm39)	M1L	possibly damaging	Het
Eml5	G	A	12: 98,758,301 (GRCm39)	T1875M	probably damaging	Het
Fam186a	A	G	15: 99,840,977 (GRCm39)	S1756P	possibly damaging	Het
Gm5431	T	A	11: 48,779,866 (GRCm39)	Q630L	probably benign	Het
H6pd	A	G	4: 150,066,512 (GRCm39)	S625P	possibly damaging	Het
Itgb4	C	T	11: 115,874,983 (GRCm39)	R447W	probably benign	Het
Kcnj6	G	T	16: 94,633,518 (GRCm39)	P180T	probably damaging	Het
Lpin3	T	A	2: 160,738,981 (GRCm39)	M263K	probably benign	Het
Lrp2	A	T	2: 69,331,834 (GRCm39)	D1640E	probably damaging	Het
Lypd2	C	T	15: 74,604,347 (GRCm39)	A74T	probably benign	Het
Map4k1	T	C	7: 28,688,257 (GRCm39)	L223P	probably damaging	Het
Myh7	A	T	14: 55,223,199 (GRCm39)	Y715*	probably null	Het
Myo9b	T	C	8: 71,808,483 (GRCm39)	S1697P	probably damaging	Het
Neb	T	C	2: 52,171,510 (GRCm39)	E1661G	probably damaging	Het
Nek8	A	T	11: 78,063,765 (GRCm39)	M80K	probably damaging	Het
Nup188	T	A	2: 30,220,947 (GRCm39)	L979Q	probably damaging	Het
Or4c113	A	T	2: 88,885,431 (GRCm39)	V113D	probably damaging	Het
P4htm	T	A	9: 108,459,141 (GRCm39)	S264C	possibly damaging	Het
Pcdha8	A	G	18: 37,126,768 (GRCm39)	T417A	probably benign	Het
Pclo	T	C	5: 14,727,406 (GRCm39)		probably benign	Het
Prox1	T	A	1: 189,893,476 (GRCm39)	N323I	possibly damaging	Het
Prune2	A	T	19: 17,177,274 (GRCm39)	R222S	probably damaging	Het
Psmd2	C	A	16: 20,471,448 (GRCm39)	R100S	possibly damaging	Het
Qrich2	A	T	11: 116,337,599 (GRCm39)	M1963K	probably damaging	Het
Rbm39	C	T	2: 156,001,082 (GRCm39)	G324D	probably damaging	Het
Rhobtb1	A	T	10: 69,105,731 (GRCm39)		probably null	Het
Rhov	G	T	2: 119,101,568 (GRCm39)	P13T	unknown	Het
Sec14l3	A	G	11: 4,025,209 (GRCm39)	D273G	possibly damaging	Het
Sirpd	T	A	3: 15,385,639 (GRCm39)	R88*	probably null	Het
Slco2a1	T	A	9: 102,927,365 (GRCm39)	I86N	probably damaging	Het
Smg1	A	T	7: 117,812,235 (GRCm39)	S19T	probably benign	Het
Stk32a	T	C	18: 43,438,082 (GRCm39)	S194P	probably benign	Het
Syna	G	A	5: 134,588,424 (GRCm39)	S175L	possibly damaging	Het
Taf4	G	A	2: 179,573,822 (GRCm39)	T682M	probably damaging	Het
Tmem151b	T	C	17: 45,858,045 (GRCm39)	Y67C	probably damaging	Het
Tshz1	C	T	18: 84,033,592 (GRCm39)	R272Q	probably damaging	Het
Tti1	A	G	2: 157,850,115 (GRCm39)	S375P	probably damaging	Het
Vcan	T	C	13: 89,873,636 (GRCm39)	K73E	probably damaging	Het
Vmn2r10	A	G	5: 109,154,286 (GRCm39)	V6A	probably benign	Het
Zfhx4	A	G	3: 5,307,107 (GRCm39)	D111G	probably damaging	Het
Zhx1	C	G	15: 57,917,470 (GRCm39)	G259R	probably damaging	Het

Other mutations in Vmn1r202

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01472:Vmn1r202	APN	13	22,686,159 (GRCm39)	missense	possibly damaging	0.95
IGL01516:Vmn1r202	APN	13	22,685,632 (GRCm39)	missense	possibly damaging	0.57
IGL01722:Vmn1r202	APN	13	22,685,890 (GRCm39)	missense	probably benign	0.00
IGL02641:Vmn1r202	APN	13	22,686,274 (GRCm39)	missense	probably benign	0.34
IGL02863:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL02876:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL02891:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL02943:Vmn1r202	APN	13	22,686,364 (GRCm39)	missense	probably benign	0.01
IGL03057:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL03114:Vmn1r202	APN	13	22,685,500 (GRCm39)	utr 3 prime	probably benign
IGL03114:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL03143:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL03159:Vmn1r202	APN	13	22,685,640 (GRCm39)	missense	probably benign	0.00
IGL03097:Vmn1r202	UTSW	13	22,685,640 (GRCm39)	missense	probably benign	0.00
R0611:Vmn1r202	UTSW	13	22,685,824 (GRCm39)	missense	probably damaging	1.00
R1350:Vmn1r202	UTSW	13	22,685,886 (GRCm39)	missense	probably benign	0.04
R1666:Vmn1r202	UTSW	13	22,685,540 (GRCm39)	missense	possibly damaging	0.94
R1668:Vmn1r202	UTSW	13	22,685,540 (GRCm39)	missense	possibly damaging	0.94
R1803:Vmn1r202	UTSW	13	22,686,313 (GRCm39)	missense	probably benign	0.00
R2035:Vmn1r202	UTSW	13	22,685,772 (GRCm39)	missense	probably damaging	0.98
R2112:Vmn1r202	UTSW	13	22,685,904 (GRCm39)	missense	possibly damaging	0.76
R2145:Vmn1r202	UTSW	13	22,685,953 (GRCm39)	missense	possibly damaging	0.79
R3026:Vmn1r202	UTSW	13	22,685,932 (GRCm39)	missense	probably benign	0.03
R3808:Vmn1r202	UTSW	13	22,686,070 (GRCm39)	missense	possibly damaging	0.83
R4714:Vmn1r202	UTSW	13	22,685,977 (GRCm39)	missense	probably damaging	1.00
R5016:Vmn1r202	UTSW	13	22,686,375 (GRCm39)	missense	probably damaging	1.00
R6136:Vmn1r202	UTSW	13	22,685,632 (GRCm39)	missense	possibly damaging	0.90
R6365:Vmn1r202	UTSW	13	22,686,374 (GRCm39)	missense	probably benign	0.12
R6982:Vmn1r202	UTSW	13	22,685,917 (GRCm39)	missense	probably benign	0.02
R7293:Vmn1r202	UTSW	13	22,685,872 (GRCm39)	missense	probably benign	0.00
R7502:Vmn1r202	UTSW	13	22,686,188 (GRCm39)	missense	probably damaging	1.00
R7603:Vmn1r202	UTSW	13	22,685,790 (GRCm39)	missense	probably damaging	1.00
R7672:Vmn1r202	UTSW	13	22,685,850 (GRCm39)	missense	probably benign	0.45
R7822:Vmn1r202	UTSW	13	22,686,241 (GRCm39)	missense	probably damaging	1.00
R7954:Vmn1r202	UTSW	13	22,685,871 (GRCm39)	missense	probably benign	0.01
R8026:Vmn1r202	UTSW	13	22,686,314 (GRCm39)	missense	possibly damaging	0.65
R8419:Vmn1r202	UTSW	13	22,685,985 (GRCm39)	missense	probably damaging	1.00
R9079:Vmn1r202	UTSW	13	22,685,602 (GRCm39)	missense	probably benign	0.00
R9194:Vmn1r202	UTSW	13	22,686,316 (GRCm39)	missense	possibly damaging	0.48

Predicted Primers

PCR Primer
(F):5'- CTGCAGACCTGGAACTGTGAAG -3'
(R):5'- AGGAGTCAGAACCATAGCCATG -3'

Sequencing Primer
(F):5'- GGTAGAGGACACGCTTGTGATG -3'
(R):5'- TCTCCTCAGTGTGGTCCAGG -3'

Posted On

2016-06-15