Mutagenetix > Incidental Mutation

Incidental Mutation 'R1568:Vmn1r229'

175451

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r229

Ensembl Gene

ENSMUSG00000061150

Gene Name

vomeronasal 1 receptor 229

Synonyms

V1re1

MMRRC Submission

039607-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R1568 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

21034757-21035677 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 21035067 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 104 (V104D)

Ref Sequence

ENSEMBL: ENSMUSP00000076045 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076759]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000076759
AA Change: V104D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000076045
Gene: ENSMUSG00000061150
AA Change: V104D

Domain	Start	End	E-Value	Type
Pfam:TAS2R	3	286	2.7e-13	PFAM
Pfam:7tm_1	22	285	4.3e-10	PFAM
Pfam:V1R	31	293	6.6e-29	PFAM

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.8%
20x: 90.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam18	T	G	8: 25,137,799 (GRCm39)		probably null	Het
Adgb	A	T	10: 10,318,409 (GRCm39)	Y138*	probably null	Het
Adra1d	T	C	2: 131,388,092 (GRCm39)	R488G	possibly damaging	Het
Ahnak	G	A	19: 8,979,739 (GRCm39)	G341E	probably damaging	Het
Ankmy1	T	C	1: 92,808,838 (GRCm39)	D690G	probably damaging	Het
Arhgef38	C	T	3: 132,838,225 (GRCm39)	E21K	probably damaging	Het
Atp8b2	T	C	3: 89,857,155 (GRCm39)	M402V	probably damaging	Het
Atp8b4	G	T	2: 126,167,314 (GRCm39)	H1062N	probably benign	Het
Bdnf	A	G	2: 109,554,139 (GRCm39)	H131R	probably damaging	Het
Cblb	C	T	16: 51,956,192 (GRCm39)	T265M	probably damaging	Het
Cenpe	T	A	3: 134,945,519 (GRCm39)	M1011K	probably benign	Het
Clca3a2	A	T	3: 144,781,410 (GRCm39)	Y711*	probably null	Het
Clca4a	A	G	3: 144,658,690 (GRCm39)	Y842H	probably benign	Het
Clspn	T	A	4: 126,475,310 (GRCm39)	M1021K	probably benign	Het
Cpne8	G	T	15: 90,503,845 (GRCm39)	R107S	probably damaging	Het
D6Ertd527e	C	G	6: 87,088,506 (GRCm39)	T223S	unknown	Het
Dna2	C	T	10: 62,784,966 (GRCm39)	R28W	probably benign	Het
Dnah5	T	A	15: 28,409,323 (GRCm39)	N3580K	probably damaging	Het
Dsp	T	C	13: 38,359,123 (GRCm39)	I298T	probably damaging	Het
Dync2h1	T	C	9: 7,157,553 (GRCm39)	K858R	probably null	Het
Fasn	A	T	11: 120,704,075 (GRCm39)	V1448E	possibly damaging	Het
Ghdc	A	G	11: 100,659,331 (GRCm39)	I322T	probably benign	Het
Gins2	T	C	8: 121,308,939 (GRCm39)	D105G	probably damaging	Het
Insr	A	T	8: 3,215,576 (GRCm39)	D975E	probably benign	Het
Klrc3	T	C	6: 129,616,510 (GRCm39)	D169G	probably benign	Het
Krt76	T	A	15: 101,793,443 (GRCm39)	S532C	unknown	Het
Lamp3	A	T	16: 19,492,275 (GRCm39)	M323K	probably damaging	Het
Lgmn	T	C	12: 102,360,868 (GRCm39)	I423M	possibly damaging	Het
Lpgat1	A	T	1: 191,508,538 (GRCm39)	T359S	possibly damaging	Het
Lrguk	T	A	6: 34,063,373 (GRCm39)	I466N	probably damaging	Het
Magi3	A	C	3: 103,996,843 (GRCm39)	M234R	probably benign	Het
Myh14	G	A	7: 44,261,122 (GRCm39)	R1042*	probably null	Het
Nfia	T	G	4: 97,999,461 (GRCm39)	Y378D	possibly damaging	Het
Npffr1	T	A	10: 61,462,012 (GRCm39)	S383T	possibly damaging	Het
Or4f57	C	A	2: 111,790,585 (GRCm39)	V278F	probably benign	Het
Or52n4	T	A	7: 104,293,977 (GRCm39)	I199F	probably benign	Het
Or5b112	C	A	19: 13,319,539 (GRCm39)	P139Q	probably benign	Het
Or9s14	T	C	1: 92,535,676 (GRCm39)	L39P	probably damaging	Het
Osr1	G	A	12: 9,629,798 (GRCm39)		probably null	Het
Pde4b	A	C	4: 102,454,896 (GRCm39)	R375S	probably damaging	Het
Pde8a	A	G	7: 80,942,011 (GRCm39)	E150G	probably damaging	Het
Pkhd1l1	A	T	15: 44,408,897 (GRCm39)		probably null	Het
Ppp3ca	A	G	3: 136,634,305 (GRCm39)	T422A	probably benign	Het
Proser1	T	C	3: 53,385,180 (GRCm39)	V354A	possibly damaging	Het
Rgs20	G	T	1: 5,091,050 (GRCm39)	R127S	probably benign	Het
Sanbr	T	C	11: 23,539,971 (GRCm39)	K48E	probably damaging	Het
Sec22a	T	C	16: 35,167,998 (GRCm39)	D171G	probably benign	Het
Secisbp2	A	G	13: 51,827,143 (GRCm39)	E417G	possibly damaging	Het
Serpinb6b	T	C	13: 33,158,895 (GRCm39)	L32S	probably damaging	Het
Sf3b1	C	G	1: 55,058,554 (GRCm39)	E12Q	possibly damaging	Het
Slc39a10	A	T	1: 46,865,375 (GRCm39)	S487T	probably benign	Het
Slc6a1	G	T	6: 114,284,731 (GRCm39)	G263V	probably damaging	Het
Spag6	A	G	2: 18,737,925 (GRCm39)	D265G	probably benign	Het
Spata31e2	T	C	1: 26,724,950 (GRCm39)	T77A	probably benign	Het
Sybu	G	T	15: 44,582,228 (GRCm39)	S132*	probably null	Het
Virma	T	C	4: 11,528,776 (GRCm39)	S1288P	probably damaging	Het
Vmn1r238	T	C	18: 3,123,358 (GRCm39)	T19A	probably benign	Het
Vmn2r86	C	T	10: 130,289,010 (GRCm39)	V164I	probably benign	Het
Wfdc13	G	T	2: 164,528,854 (GRCm39)	A64S	probably damaging	Het
Zfp873	C	A	10: 81,896,113 (GRCm39)	H318Q	probably damaging	Het
Zyg11a	A	G	4: 108,040,843 (GRCm39)		probably null	Het

Other mutations in Vmn1r229

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0682:Vmn1r229	UTSW	17	21,034,950 (GRCm39)	missense	probably benign	0.43
R1401:Vmn1r229	UTSW	17	21,034,904 (GRCm39)	missense	possibly damaging	0.63
R1484:Vmn1r229	UTSW	17	21,034,791 (GRCm39)	missense	probably damaging	1.00
R1551:Vmn1r229	UTSW	17	21,035,051 (GRCm39)	missense	probably benign	0.36
R1793:Vmn1r229	UTSW	17	21,034,974 (GRCm39)	missense	possibly damaging	0.61
R2157:Vmn1r229	UTSW	17	21,035,638 (GRCm39)	missense	possibly damaging	0.82
R4458:Vmn1r229	UTSW	17	21,034,894 (GRCm39)	missense	probably damaging	1.00
R4556:Vmn1r229	UTSW	17	21,034,953 (GRCm39)	missense	possibly damaging	0.79
R4891:Vmn1r229	UTSW	17	21,035,081 (GRCm39)	missense	probably damaging	1.00
R6310:Vmn1r229	UTSW	17	21,034,976 (GRCm39)	missense	probably benign	0.01
R6995:Vmn1r229	UTSW	17	21,035,277 (GRCm39)	missense	probably damaging	1.00
R8109:Vmn1r229	UTSW	17	21,035,268 (GRCm39)	missense	probably benign	0.05
R8155:Vmn1r229	UTSW	17	21,035,472 (GRCm39)	missense	probably damaging	1.00
R8232:Vmn1r229	UTSW	17	21,035,309 (GRCm39)	missense	probably damaging	0.96
R8828:Vmn1r229	UTSW	17	21,034,990 (GRCm39)	missense	probably damaging	0.97
R8943:Vmn1r229	UTSW	17	21,035,418 (GRCm39)	missense	possibly damaging	0.91
R9147:Vmn1r229	UTSW	17	21,034,758 (GRCm39)	start codon destroyed	probably null	1.00
R9148:Vmn1r229	UTSW	17	21,034,758 (GRCm39)	start codon destroyed	probably null	1.00
R9407:Vmn1r229	UTSW	17	21,035,259 (GRCm39)	missense	probably damaging	1.00
R9621:Vmn1r229	UTSW	17	21,035,315 (GRCm39)	missense	probably benign	0.00
Z1088:Vmn1r229	UTSW	17	21,035,327 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGGCAATGGGAATTGTACTCTCACTTC -3'
(R):5'- GCAAACCAGGATCAGAATGGTCTGTG -3'

Sequencing Primer
(F):5'- CACTTGGTATTCTGGGAAACTTC -3'
(R):5'- TTTGTCACGGCCTACAGAG -3'

Posted On

2014-04-24