Mutagenetix > Incidental Mutation

Incidental Mutation 'R4736:Vmn1r71'

359244

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r71

Ensembl Gene

ENSMUSG00000059206

Gene Name

vomeronasal 1 receptor 71

Synonyms

V1re13

MMRRC Submission

041963-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

R4736 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

10481429-10483465 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 10481791 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 233 (V233D)

Ref Sequence

ENSEMBL: ENSMUSP00000153870 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000079113] [ENSMUST00000226874] [ENSMUST00000227003] [ENSMUST00000227702] [ENSMUST00000227940] [ENSMUST00000228098] [ENSMUST00000228561] [ENSMUST00000228526] [ENSMUST00000228374] [ENSMUST00000228248]

AlphaFold

Q8VIC0

Predicted Effect

possibly damaging
Transcript: ENSMUST00000079113
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000078116
Gene: ENSMUSG00000059206
AA Change: V299D

Domain	Start	End	E-Value	Type
Pfam:TAS2R	3	304	2e-8	PFAM
Pfam:7tm_1	22	289	3.1e-6	PFAM
Pfam:V1R	34	297	4.8e-28	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210233

Predicted Effect

possibly damaging
Transcript: ENSMUST00000226874
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000227003
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000227702
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000227940
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228098
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228561
AA Change: V233D

PolyPhen 2 Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228526
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228374
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228248
AA Change: V299D

PolyPhen 2 Score 0.756 (Sensitivity: 0.85; Specificity: 0.92)

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.9%
20x: 94.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	T	C	3: 137,774,246 (GRCm39)	I1145T	probably damaging	Het
Aadat	T	C	8: 60,993,140 (GRCm39)	V360A	probably benign	Het
Abhd16a	A	T	17: 35,320,859 (GRCm39)	T436S	probably benign	Het
Acbd5	G	T	2: 22,989,596 (GRCm39)	L406F	probably damaging	Het
Agrn	G	A	4: 156,256,858 (GRCm39)	T1142M	probably benign	Het
Aig1	C	A	10: 13,677,674 (GRCm39)	W106L	probably damaging	Het
Akr1d1	T	C	6: 37,534,535 (GRCm39)		probably null	Het
Ap1g1	G	A	8: 110,581,714 (GRCm39)	D658N	possibly damaging	Het
Arhgap45	A	G	10: 79,862,006 (GRCm39)	Y520C	probably damaging	Het
Arhgap5	A	T	12: 52,565,860 (GRCm39)	M944L	probably benign	Het
Asic5	C	T	3: 81,907,116 (GRCm39)	T47I	possibly damaging	Het
Cabp5	A	G	7: 13,134,664 (GRCm39)		probably null	Het
Ccr6	A	T	17: 8,474,896 (GRCm39)	R34*	probably null	Het
Cdin1	A	G	2: 115,412,369 (GRCm39)	I2V	probably benign	Het
Clec4a2	T	C	6: 123,117,622 (GRCm39)	I180T	probably damaging	Het
Cmtr1	A	G	17: 29,919,216 (GRCm39)	E704G	possibly damaging	Het
Cyth3	G	A	5: 143,670,234 (GRCm39)		probably null	Het
Dbt	T	C	3: 116,332,781 (GRCm39)	I200T	probably damaging	Het
Dennd6b	T	C	15: 89,069,795 (GRCm39)	H468R	probably benign	Het
Depdc5	A	G	5: 33,132,666 (GRCm39)	M1237V	probably benign	Het
Dpp6	A	G	5: 27,917,657 (GRCm39)	Y616C	probably damaging	Het
Dync2h1	A	T	9: 7,006,862 (GRCm39)	S3710T	probably benign	Het
Eif4g3	T	A	4: 137,925,408 (GRCm39)	S1584T	probably benign	Het
Emc3	G	A	6: 113,508,310 (GRCm39)	T45I	possibly damaging	Het
Esf1	T	A	2: 139,966,891 (GRCm39)	D685V	probably damaging	Het
Ezr	A	G	17: 7,008,975 (GRCm39)	S366P	probably benign	Het
Gbe1	C	T	16: 70,292,141 (GRCm39)	A491V	probably damaging	Het
Haus6	A	G	4: 86,518,986 (GRCm39)		probably null	Het
Heca	G	A	10: 17,790,935 (GRCm39)	Q12*	probably null	Het
Hpdl	T	C	4: 116,678,221 (GRCm39)	N80S	probably damaging	Het
Hydin	A	T	8: 111,249,840 (GRCm39)	Q2261L	probably benign	Het
Itgae	G	T	11: 73,005,706 (GRCm39)	R290L	possibly damaging	Het
Kcna10	C	A	3: 107,102,808 (GRCm39)	L480I	probably benign	Het
Kif27	T	C	13: 58,476,785 (GRCm39)	T622A	probably benign	Het
Lama2	T	C	10: 27,080,925 (GRCm39)	N966S	probably damaging	Het
Mdfic	A	G	6: 15,741,019 (GRCm39)	K38E	possibly damaging	Het
Med25	G	A	7: 44,541,712 (GRCm39)	A26V	probably damaging	Het
Mrpl19	A	T	6: 81,941,329 (GRCm39)	S77R	probably damaging	Het
Mtcl2	T	A	2: 156,862,474 (GRCm39)	D1485V	probably damaging	Het
Mybpc2	T	C	7: 44,161,971 (GRCm39)	D493G	probably damaging	Het
Myh4	A	G	11: 67,131,746 (GRCm39)	T69A	probably benign	Het
Myo16	G	T	8: 10,423,527 (GRCm39)	G288W	probably damaging	Het
Myo9b	T	C	8: 71,809,236 (GRCm39)	L1815P	probably damaging	Het
Myom2	T	A	8: 15,131,271 (GRCm39)	L323Q	probably damaging	Het
Naip1	T	C	13: 100,581,034 (GRCm39)	D71G	possibly damaging	Het
Nktr	T	A	9: 121,578,805 (GRCm39)		probably benign	Het
Nol10	A	G	12: 17,405,288 (GRCm39)	K88E	probably damaging	Het
Nol4	T	C	18: 22,852,050 (GRCm39)	D505G	probably damaging	Het
Nynrin	T	A	14: 56,101,454 (GRCm39)	N374K	probably damaging	Het
Obscn	A	T	11: 58,954,362 (GRCm39)	L3740Q	probably damaging	Het
Or5g23	T	C	2: 85,438,327 (GRCm39)	H309R	probably benign	Het
Otub2	T	A	12: 103,359,103 (GRCm39)	L64Q	probably benign	Het
Pgm5	G	A	19: 24,812,169 (GRCm39)	A121V	probably damaging	Het
Pi4ka	A	T	16: 17,195,039 (GRCm39)	Y120N	probably benign	Het
Rpl36al	G	A	12: 69,229,732 (GRCm39)	A60V	possibly damaging	Het
Rspo4	T	C	2: 151,685,054 (GRCm39)	Y21H	probably benign	Het
Scube2	A	G	7: 109,430,412 (GRCm39)	V455A	probably benign	Het
Serpina1f	T	C	12: 103,659,805 (GRCm39)	D159G	probably damaging	Het
Sf1	A	G	19: 6,415,694 (GRCm39)	D11G	probably damaging	Het
Siglecg	T	C	7: 43,067,332 (GRCm39)	F633S	probably benign	Het
Skic2	A	G	17: 35,067,173 (GRCm39)	S89P	possibly damaging	Het
Slc22a13	T	C	9: 119,022,698 (GRCm39)	E501G	probably damaging	Het
Slc44a3	A	G	3: 121,303,855 (GRCm39)	S294P	probably damaging	Het
Smad3	T	G	9: 63,664,842 (GRCm39)	K40Q	probably damaging	Het
Stt3a	T	A	9: 36,661,008 (GRCm39)	M268L	probably benign	Het
Taf4	A	T	2: 179,566,287 (GRCm39)	V817E	probably damaging	Het
Tgfbr1	A	G	4: 47,383,835 (GRCm39)	T58A	probably benign	Het
Trpc6	T	C	9: 8,609,871 (GRCm39)	V113A	probably damaging	Het
Ttll13	T	A	7: 79,898,024 (GRCm39)		probably null	Het
Uba7	T	C	9: 107,857,364 (GRCm39)	L742P	probably benign	Het
Ulk2	A	G	11: 61,724,261 (GRCm39)	L174P	probably damaging	Het
Unc5c	A	T	3: 141,522,692 (GRCm39)	Y706F	probably benign	Het
Unc80	A	T	1: 66,688,831 (GRCm39)		probably null	Het
Usp34	T	A	11: 23,343,749 (GRCm39)		probably null	Het
Xpo6	T	C	7: 125,739,755 (GRCm39)	K439R	probably benign	Het
Xrn1	G	T	9: 95,915,689 (GRCm39)	G1271C	probably damaging	Het
Yes1	A	T	5: 32,818,121 (GRCm39)	E386V	probably damaging	Het
Zfp759	C	A	13: 67,287,408 (GRCm39)	H320N	probably damaging	Het
Zfp990	A	T	4: 145,263,512 (GRCm39)	H170L	possibly damaging	Het

Other mutations in Vmn1r71

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00984:Vmn1r71	APN	7	10,482,046 (GRCm39)	missense	probably damaging	0.99
IGL01921:Vmn1r71	APN	7	10,482,199 (GRCm39)	missense	probably benign	0.16
IGL02397:Vmn1r71	APN	7	10,482,199 (GRCm39)	missense	probably benign	0.27
IGL02654:Vmn1r71	APN	7	10,482,242 (GRCm39)	missense	probably benign	0.42
IGL02900:Vmn1r71	APN	7	10,482,601 (GRCm39)	missense	probably benign	0.28
IGL03236:Vmn1r71	APN	7	10,482,211 (GRCm39)	missense	probably benign	0.11
IGL03269:Vmn1r71	APN	7	10,482,571 (GRCm39)	missense	possibly damaging	0.88
FR4976:Vmn1r71	UTSW	7	10,482,048 (GRCm39)	missense	probably benign
R0389:Vmn1r71	UTSW	7	10,482,238 (GRCm39)	missense	probably benign	0.05
R0443:Vmn1r71	UTSW	7	10,482,238 (GRCm39)	missense	probably benign	0.05
R0470:Vmn1r71	UTSW	7	10,482,019 (GRCm39)	missense	possibly damaging	0.64
R0471:Vmn1r71	UTSW	7	10,482,019 (GRCm39)	missense	possibly damaging	0.64
R0472:Vmn1r71	UTSW	7	10,482,019 (GRCm39)	missense	possibly damaging	0.64
R0567:Vmn1r71	UTSW	7	10,482,556 (GRCm39)	missense	probably damaging	1.00
R1498:Vmn1r71	UTSW	7	10,482,575 (GRCm39)	missense	probably benign	0.01
R1745:Vmn1r71	UTSW	7	10,482,196 (GRCm39)	missense	probably benign	0.05
R2350:Vmn1r71	UTSW	7	10,481,846 (GRCm39)	missense	probably benign	0.00
R2970:Vmn1r71	UTSW	7	10,482,641 (GRCm39)	missense	possibly damaging	0.67
R3522:Vmn1r71	UTSW	7	10,481,792 (GRCm39)	missense	probably benign	0.03
R4193:Vmn1r71	UTSW	7	10,482,175 (GRCm39)	missense	possibly damaging	0.55
R5115:Vmn1r71	UTSW	7	10,481,885 (GRCm39)	missense	probably benign	0.00
R6108:Vmn1r71	UTSW	7	10,482,545 (GRCm39)	missense	probably benign	0.01
R6455:Vmn1r71	UTSW	7	10,482,331 (GRCm39)	missense	probably benign	0.01
R6582:Vmn1r71	UTSW	7	10,482,608 (GRCm39)	missense	probably benign	0.00
R6696:Vmn1r71	UTSW	7	10,482,401 (GRCm39)	missense	probably damaging	0.96
R6778:Vmn1r71	UTSW	7	10,482,143 (GRCm39)	missense	probably benign	0.02
R7347:Vmn1r71	UTSW	7	10,482,428 (GRCm39)	missense	not run
R7631:Vmn1r71	UTSW	7	10,482,378 (GRCm39)	missense	probably damaging	1.00
R7795:Vmn1r71	UTSW	7	10,482,136 (GRCm39)	missense	probably damaging	0.98
R7820:Vmn1r71	UTSW	7	10,482,652 (GRCm39)	missense	possibly damaging	0.85
R7836:Vmn1r71	UTSW	7	10,482,277 (GRCm39)	missense	possibly damaging	0.51

Predicted Primers

PCR Primer
(F):5'- ACACTCAAGAGGCAGGTGATAC -3'
(R):5'- GTTCCAGTCGATATTCCCCAG -3'

Sequencing Primer
(F):5'- GGCAGGTGATACAAATAAATACCC -3'
(R):5'- GTCGATATTCCCCAGAGTCCAGAG -3'

Posted On

2015-11-11