Mutagenetix > Incidental Mutations

Incidental Mutation 'R5901:Vmn1r7'

456318

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r7

Ensembl Gene

ENSMUSG00000093696

Gene Name

vomeronasal 1 receptor 7

Synonyms

Gm5568, V1rc31

MMRRC Submission

043239-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.163) question?

Stock #

R5901 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

57024106-57025324 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 57024606 bp

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 223 (E223G)

Ref Sequence

ENSEMBL: ENSMUSP00000135571 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000176252]

Predicted Effect

probably damaging
Transcript: ENSMUST00000176252
AA Change: E223G

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

SMART Domains

Protein: ENSMUSP00000135571
Gene: ENSMUSG00000093696
AA Change: E223G

Domain	Start	End	E-Value	Type
Pfam:V1R	28	293	1.1e-59	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.8%
20x: 93.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2300003K06Rik	T	A	11: 99,837,337	S227C	unknown	Het
Acyp2	C	T	11: 30,506,354	E98K	possibly damaging	Het
Adamts15	C	T	9: 30,902,490	R793H	probably damaging	Het
Ankra2	A	G	13: 98,271,136	E38G	probably damaging	Het
Aqp8	G	A	7: 123,462,584	C8Y	probably damaging	Het
Atg9b	A	G	5: 24,392,019		probably benign	Het
Atp6v1b1	A	G	6: 83,758,357	E469G	possibly damaging	Het
B4gat1	T	A	19: 5,039,213	Y79*	probably null	Het
BB019430	T	A	10: 58,704,192		noncoding transcript	Het
Calhm3	T	C	19: 47,157,613	Y51C	probably damaging	Het
Ccr2	C	T	9: 124,106,202	T173I	possibly damaging	Het
Cfap43	T	C	19: 47,897,099	D359G	probably damaging	Het
Dopey2	A	G	16: 93,769,751	E1022G	possibly damaging	Het
Drd2	T	A	9: 49,406,959	C400*	probably null	Het
Efcab7	T	A	4: 99,909,744	H495Q	probably damaging	Het
Faim	T	C	9: 98,992,142	V29A	probably benign	Het
Fancd2	T	C	6: 113,549,365	S350P	probably damaging	Het
Fbxw16	T	C	9: 109,441,217	E152G	probably benign	Het
Kif17	T	C	4: 138,298,332		probably null	Het
Kif24	A	T	4: 41,428,604	S119T	probably damaging	Het
Ly6k	A	T	15: 74,798,580	S38T	probably benign	Het
Mapk10	A	G	5: 102,913,292	S430P	probably damaging	Het
Megf10	G	A	18: 57,277,108	A654T	probably benign	Het
Mlph	T	C	1: 90,939,814	L450P	probably damaging	Het
Otof	T	C	5: 30,374,979	D1603G	probably damaging	Het
Pdcd11	T	C	19: 47,128,332	S1580P	possibly damaging	Het
Rad54b	G	A	4: 11,595,919	R232H	possibly damaging	Het
Sar1b	C	T	11: 51,779,749	T40I	possibly damaging	Het
Scyl2	C	T	10: 89,660,262	S242N	probably benign	Het
Sema4b	A	G	7: 80,224,967	N702D	possibly damaging	Het
Slc16a11	A	G	11: 70,216,346	I394V	probably benign	Het
Stard9	A	C	2: 120,701,370	T2703P	probably damaging	Het
Stat5b	A	T	11: 100,804,907	L83Q	possibly damaging	Het
Tas2r119	T	A	15: 32,177,786	V166D	possibly damaging	Het
Tmem117	T	A	15: 94,714,958	I125N	probably benign	Het
Tmem39a	T	C	16: 38,573,206	I89T	probably benign	Het
Ubr4	T	A	4: 139,451,254	H3272Q	probably damaging	Het
Vmn2r78	T	C	7: 86,954,588	V658A	probably damaging	Het
Xirp2	A	T	2: 67,513,066	T1884S	possibly damaging	Het
Xkr4	A	T	1: 3,216,678	F430I	probably damaging	Het
Yae1d1	A	G	13: 17,989,615	M1T	probably null	Het
Zfand4	T	C	6: 116,288,123	V183A	probably damaging	Het

Other mutations in Vmn1r7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01382:Vmn1r7	APN	6	57024723	missense	probably damaging	1.00
IGL01528:Vmn1r7	APN	6	57024547	missense	probably benign
IGL02024:Vmn1r7	APN	6	57024889	missense	probably benign	0.01
IGL02234:Vmn1r7	APN	6	57024552	missense	probably damaging	0.98
IGL02610:Vmn1r7	APN	6	57025052	missense	probably benign	0.01
IGL02691:Vmn1r7	APN	6	57024388	missense	probably benign	0.05
R0529:Vmn1r7	UTSW	6	57024465	missense	possibly damaging	0.78
R0548:Vmn1r7	UTSW	6	57025081	missense	probably damaging	0.96
R1254:Vmn1r7	UTSW	6	57024787	missense	probably damaging	1.00
R1279:Vmn1r7	UTSW	6	57024949	missense	possibly damaging	0.63
R1582:Vmn1r7	UTSW	6	57025158	missense	probably damaging	1.00
R1973:Vmn1r7	UTSW	6	57025026	missense	probably benign	0.00
R1991:Vmn1r7	UTSW	6	57024868	missense	probably benign	0.37
R2160:Vmn1r7	UTSW	6	57024894	missense	probably damaging	0.97
R3546:Vmn1r7	UTSW	6	57024849	missense	possibly damaging	0.80
R3547:Vmn1r7	UTSW	6	57024849	missense	possibly damaging	0.80
R6294:Vmn1r7	UTSW	6	57024419	missense	probably benign	0.00
R7063:Vmn1r7	UTSW	6	57024433	missense	possibly damaging	0.63
R7192:Vmn1r7	UTSW	6	57024467	missense	probably benign	0.00
R7647:Vmn1r7	UTSW	6	57025270	missense	probably benign	0.01
R7781:Vmn1r7	UTSW	6	57024568	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- CAGAACTGATTTGTACCAAAGGGG -3'
(R):5'- ATGTGAGTGAGACCAACCAG -3'

Sequencing Primer
(F):5'- GTAATTGTGGGATAGGCATACATC -3'
(R):5'- TGAGACCAACCAGATGCAGGTC -3'

Posted On

2017-02-15