Mutagenetix > Incidental Mutation

Incidental Mutation 'R5800:Vmn1r237'

447372

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r237

Ensembl Gene

ENSMUSG00000058030

Gene Name

vomeronasal 1 receptor 237

Synonyms

V1rf3

MMRRC Submission

043389-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R5800 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

21313963-21314912 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 21314807 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 264 (T264S)

Ref Sequence

ENSEMBL: ENSMUSP00000076531 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077301]

AlphaFold

Q8R296

Predicted Effect

probably benign
Transcript: ENSMUST00000077301
AA Change: T264S

PolyPhen 2 Score 0.055 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000076531
Gene: ENSMUSG00000058030
AA Change: T264S

Domain	Start	End	E-Value	Type
Pfam:TAS2R	1	289	7.1e-17	PFAM
Pfam:V1R	34	289	1.9e-34	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.3%
20x: 95.4%

Validation Efficiency

96% (50/52)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1520401A03Rik	G	A	17: 23,717,992	P72S	probably damaging	Het
4932438A13Rik	A	G	3: 37,052,443	D4974G	probably damaging	Het
Abca12	A	T	1: 71,321,432	V540D	possibly damaging	Het
Adamts8	A	T	9: 30,954,482	D442V	probably damaging	Het
Casp4	G	A	9: 5,308,915		probably null	Het
Cfap45	T	A	1: 172,538,600	V30E	probably damaging	Het
Col6a4	A	G	9: 106,080,275	F117L	probably damaging	Het
Dnah7c	A	T	1: 46,647,015	T1810S	probably benign	Het
Drosha	C	T	15: 12,865,067	T627M	probably damaging	Het
Drosha	C	A	15: 12,902,647	A1001D	probably damaging	Het
Efhc1	G	A	1: 20,978,781	V473I	probably benign	Het
Ephx2	T	C	14: 66,107,302	K191R	probably benign	Het
Ero1lb	T	A	13: 12,602,301		probably null	Het
Esyt2	A	T	12: 116,370,188	D837V	possibly damaging	Het
Fip1l1	T	A	5: 74,546,081	D126E	possibly damaging	Het
Fyttd1	C	T	16: 32,891,288	R86C	probably damaging	Het
Gm12888	T	A	4: 121,319,428	T59S	probably damaging	Het
Gm34653	T	C	2: 34,838,642	F151S	possibly damaging	Het
Gm7353	A	T	7: 3,110,168		noncoding transcript	Het
Gpr153	C	T	4: 152,280,077	Q197*	probably null	Het
H2-T23	G	T	17: 36,031,604		probably benign	Het
Ighv1-16	T	A	12: 114,665,911	R85S	probably benign	Het
Ipcef1	T	A	10: 6,890,569	D376V	probably damaging	Het
Kdm1a	T	A	4: 136,573,070		probably null	Het
Klk1b27	A	T	7: 44,055,664	Q85L	probably benign	Het
Krt39	A	T	11: 99,521,145	D38E	probably benign	Het
L1td1	T	C	4: 98,733,762	L187P	possibly damaging	Het
Lrrc8b	C	T	5: 105,481,342	S518L	probably benign	Het
Lyg1	C	T	1: 37,946,953	D176N	probably damaging	Het
Mctp1	A	G	13: 76,688,559	N82D	probably damaging	Het
Muc6	T	C	7: 141,640,423		probably benign	Het
Nynrin	T	C	14: 55,870,631	L1065P	probably damaging	Het
Olfr1474	T	C	19: 13,471,896	S309P	probably benign	Het
Pcdh7	T	A	5: 57,722,225	S1041T	probably damaging	Het
Pkd1l1	T	A	11: 8,861,302	M1518L	probably benign	Het
Prl8a6	G	T	13: 27,435,470	Q90K	probably benign	Het
Ptcd1	T	A	5: 145,159,665	D206V	probably damaging	Het
Rap1gap	C	A	4: 137,720,377	D478E	probably benign	Het
Scn5a	A	G	9: 119,501,666	Y1269H	probably damaging	Het
Sdc2	A	T	15: 33,028,144	H136L	probably benign	Het
Senp6	A	T	9: 80,126,433	I120F	probably damaging	Het
Shisa5	G	A	9: 109,056,094		probably null	Het
Slc19a1	A	G	10: 77,042,269	S213G	probably null	Het
Smim8	TTTAATGAAGAGCT	TT	4: 34,771,261		probably benign	Het
Tbc1d20	T	A	2: 152,308,325		probably null	Het
Tll2	T	C	19: 41,104,934	H481R	probably benign	Het
Tmc7	A	G	7: 118,539,440	V692A	probably benign	Het
Tmem234	T	C	4: 129,607,131		probably null	Het
Vmn2r98	A	T	17: 19,065,998	T253S	probably benign	Het
Zfyve27	T	C	19: 42,182,663	Y191H	probably damaging	Het

Other mutations in Vmn1r237

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01300:Vmn1r237	APN	17	21314075	missense	probably damaging	0.97
IGL02746:Vmn1r237	APN	17	21314218	missense	possibly damaging	0.96
IGL03112:Vmn1r237	APN	17	21314106	nonsense	probably null
IGL03351:Vmn1r237	APN	17	21314837	missense	probably benign	0.06
BB009:Vmn1r237	UTSW	17	21314463	missense	probably benign	0.01
BB019:Vmn1r237	UTSW	17	21314463	missense	probably benign	0.01
R0478:Vmn1r237	UTSW	17	21314819	missense	probably damaging	1.00
R0514:Vmn1r237	UTSW	17	21314670	missense	possibly damaging	0.63
R0616:Vmn1r237	UTSW	17	21314623	missense	probably damaging	1.00
R0865:Vmn1r237	UTSW	17	21314714	missense	probably damaging	0.99
R1590:Vmn1r237	UTSW	17	21314039	missense	probably damaging	0.99
R3022:Vmn1r237	UTSW	17	21314447	missense	probably damaging	0.99
R4241:Vmn1r237	UTSW	17	21314663	missense	possibly damaging	0.63
R4242:Vmn1r237	UTSW	17	21314663	missense	possibly damaging	0.63
R4646:Vmn1r237	UTSW	17	21314138	missense	probably benign	0.02
R5144:Vmn1r237	UTSW	17	21314426	missense	possibly damaging	0.96
R5229:Vmn1r237	UTSW	17	21314371	missense	probably benign	0.00
R5334:Vmn1r237	UTSW	17	21314680	missense	probably benign	0.00
R5898:Vmn1r237	UTSW	17	21314551	missense	probably damaging	0.99
R6190:Vmn1r237	UTSW	17	21314294	missense	probably damaging	1.00
R6472:Vmn1r237	UTSW	17	21314354	missense	probably benign	0.16
R6811:Vmn1r237	UTSW	17	21314386	missense	probably benign	0.02
R7932:Vmn1r237	UTSW	17	21314463	missense	probably benign	0.01
R8008:Vmn1r237	UTSW	17	21314194	missense	probably damaging	1.00
R8086:Vmn1r237	UTSW	17	21314247	missense	possibly damaging	0.61
R9568:Vmn1r237	UTSW	17	21314515	missense	probably benign
R9631:Vmn1r237	UTSW	17	21314398	missense	probably benign	0.28
X0011:Vmn1r237	UTSW	17	21314055	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- TCCAGTGGCTACATGGTTTG -3'
(R):5'- CACCACCTGCTTTTGTGACATG -3'

Sequencing Primer
(F):5'- GTATTCTTTACAGACATAAGCAGAGG -3'
(R):5'- CACCTGCTTTTGTGACATGATTGAG -3'

Posted On

2016-12-15