Mutagenetix > Incidental Mutation

Incidental Mutation 'R6868:Vmn1r184'

536019

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r184

Ensembl Gene

ENSMUSG00000046130

Gene Name

vomeronasal 1 receptor, 184

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R6868 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

25966256-25967200 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 25966727 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 158 (M158L)

Ref Sequence

ENSEMBL: ENSMUSP00000154576 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057123] [ENSMUST00000227230] [ENSMUST00000227232] [ENSMUST00000227534] [ENSMUST00000227790] [ENSMUST00000228145] [ENSMUST00000228369]

AlphaFold

E9Q2N4

Predicted Effect

probably benign
Transcript: ENSMUST00000057123
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000061885
Gene: ENSMUSG00000046130
AA Change: M158L

Domain	Start	End	E-Value	Type
Pfam:TAS2R	8	308	1.7e-7	PFAM
Pfam:V1R	35	297	7.5e-31	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000227230
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Predicted Effect

probably benign
Transcript: ENSMUST00000227232
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Predicted Effect

probably benign
Transcript: ENSMUST00000227534
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Predicted Effect

probably benign
Transcript: ENSMUST00000227790
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Predicted Effect

probably benign
Transcript: ENSMUST00000228145
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Predicted Effect

probably benign
Transcript: ENSMUST00000228369
AA Change: M158L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630010A05Rik	A	T	16: 14,436,559 (GRCm39)	N204I	probably damaging	Het
Aasdh	C	T	5: 77,039,527 (GRCm39)	V261M	probably damaging	Het
Adgrg7	A	G	16: 56,593,839 (GRCm39)	F126L	probably benign	Het
Agxt2	T	C	15: 10,373,855 (GRCm39)	L87P	probably damaging	Het
Alcam	G	A	16: 52,088,748 (GRCm39)	S554F	probably damaging	Het
Ambra1	T	C	2: 91,747,878 (GRCm39)	S1205P	possibly damaging	Het
Bst2	A	C	8: 71,987,404 (GRCm39)	V150G	unknown	Het
C3	T	C	17: 57,511,029 (GRCm39)	Y1659C	possibly damaging	Het
Cacna1s	G	A	1: 136,020,432 (GRCm39)	R823Q	probably benign	Het
Cdk4	T	C	10: 126,900,870 (GRCm39)	V174A	probably benign	Het
Ces2h	T	A	8: 105,745,055 (GRCm39)	N396K	probably benign	Het
Cfap144	C	T	11: 58,683,732 (GRCm39)	D113N	probably damaging	Het
Chd7	T	C	4: 8,811,501 (GRCm39)		probably null	Het
Cnih4	A	G	1: 180,993,762 (GRCm39)	I76V	probably null	Het
Csmd2	G	A	4: 128,336,633 (GRCm39)	V1404I	probably benign	Het
Ctrb1	T	C	8: 112,416,035 (GRCm39)	D53G	probably benign	Het
Cul9	C	A	17: 46,833,109 (GRCm39)	R1323L	possibly damaging	Het
Dchs1	A	G	7: 105,412,710 (GRCm39)	V1230A	possibly damaging	Het
Dgat2	T	C	7: 98,807,513 (GRCm39)	D219G	probably benign	Het
Dgkh	T	C	14: 78,862,293 (GRCm39)	T225A	probably damaging	Het
Dock9	G	T	14: 121,823,676 (GRCm39)	A1412E	probably benign	Het
Dscam	C	T	16: 96,631,140 (GRCm39)	V292M	probably damaging	Het
Fras1	T	A	5: 96,830,237 (GRCm39)	V1509E	probably benign	Het
Fryl	T	C	5: 73,226,146 (GRCm39)	Q1839R	probably damaging	Het
Gcat	A	G	15: 78,919,566 (GRCm39)	D177G	probably damaging	Het
Gss	T	C	2: 155,409,732 (GRCm39)	T235A	possibly damaging	Het
Ints10	T	A	8: 69,250,450 (GRCm39)	M114K	probably damaging	Het
Ints5	T	G	19: 8,874,750 (GRCm39)	L903R	probably damaging	Het
Lipo2	G	T	19: 33,725,862 (GRCm39)	P130Q	possibly damaging	Het
Megf11	G	A	9: 64,587,591 (GRCm39)	C494Y	probably damaging	Het
Milr1	T	C	11: 106,654,747 (GRCm39)	Y162H	probably damaging	Het
Mrc2	T	A	11: 105,219,244 (GRCm39)	I278N	probably damaging	Het
Mst1r	T	A	9: 107,793,132 (GRCm39)		probably null	Het
Myh15	G	A	16: 48,889,766 (GRCm39)	C119Y	probably damaging	Het
Nap1l1	G	A	10: 111,330,669 (GRCm39)	G358D	probably damaging	Het
Nav3	T	C	10: 109,529,027 (GRCm39)	I2178V	possibly damaging	Het
Nkx2-5	T	C	17: 27,060,268 (GRCm39)	E21G	probably damaging	Het
Nos2	C	T	11: 78,848,332 (GRCm39)	R967C	probably benign	Het
Or6c215	T	C	10: 129,638,037 (GRCm39)	D119G	probably damaging	Het
Parp10	T	C	15: 76,127,306 (GRCm39)	R44G	probably damaging	Het
Pced1b	A	G	15: 97,282,222 (GRCm39)	H87R	probably damaging	Het
Ppfia3	T	A	7: 45,003,036 (GRCm39)	L524F	probably damaging	Het
Ppp1r12b	T	C	1: 134,814,176 (GRCm39)	T376A	probably benign	Het
Ppp4r4	T	C	12: 103,557,111 (GRCm39)	L449P	probably damaging	Het
Prkd1	T	C	12: 50,472,320 (GRCm39)	R198G	probably damaging	Het
Pth2r	C	A	1: 65,427,638 (GRCm39)	A437E	probably benign	Het
Ptprh	A	T	7: 4,604,864 (GRCm39)	I60N	probably benign	Het
Pxmp2	C	T	5: 110,433,846 (GRCm39)	R9Q	probably damaging	Het
Scarb2	T	C	5: 92,633,168 (GRCm39)	K55E	probably benign	Het
Slc18b1	T	C	10: 23,680,132 (GRCm39)	V109A	possibly damaging	Het
Slx4ip	T	A	2: 136,842,130 (GRCm39)	D18E	probably damaging	Het
Stk40	A	G	4: 126,017,607 (GRCm39)	R45G	probably damaging	Het
Tbxas1	A	T	6: 39,061,240 (GRCm39)	Q513L	probably damaging	Het
Tcf4	A	T	18: 69,790,721 (GRCm39)		probably null	Het
Tmc6	T	A	11: 117,665,143 (GRCm39)	I377F	probably benign	Het
Tmem131l	T	C	3: 83,868,938 (GRCm39)	I146V	probably damaging	Het
Trac	T	A	14: 54,458,049 (GRCm39)		probably benign	Het
Trpm7	T	C	2: 126,679,334 (GRCm39)	D409G	probably damaging	Het
Usp39	A	T	6: 72,314,734 (GRCm39)	V224E	possibly damaging	Het
Vmn2r120	T	A	17: 57,852,218 (GRCm39)	I33L	probably benign	Het

Other mutations in Vmn1r184

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01396:Vmn1r184	APN	7	25,966,862 (GRCm39)	missense	probably damaging	1.00
IGL01411:Vmn1r184	APN	7	25,966,320 (GRCm39)	missense	probably benign	0.06
IGL02961:Vmn1r184	APN	7	25,967,075 (GRCm39)	missense	probably benign	0.27
IGL03271:Vmn1r184	APN	7	25,967,034 (GRCm39)	missense	probably benign
R0302:Vmn1r184	UTSW	7	25,966,968 (GRCm39)	missense	probably damaging	1.00
R0384:Vmn1r184	UTSW	7	25,967,076 (GRCm39)	missense	probably benign	0.41
R0591:Vmn1r184	UTSW	7	25,966,500 (GRCm39)	missense	probably damaging	0.98
R0620:Vmn1r184	UTSW	7	25,966,602 (GRCm39)	missense	possibly damaging	0.46
R1644:Vmn1r184	UTSW	7	25,966,670 (GRCm39)	missense	probably benign	0.00
R2304:Vmn1r184	UTSW	7	25,966,550 (GRCm39)	missense	probably damaging	1.00
R2329:Vmn1r184	UTSW	7	25,966,387 (GRCm39)	missense	probably damaging	1.00
R3522:Vmn1r184	UTSW	7	25,967,008 (GRCm39)	nonsense	probably null
R5020:Vmn1r184	UTSW	7	25,966,955 (GRCm39)	missense	possibly damaging	0.87
R5030:Vmn1r184	UTSW	7	25,966,881 (GRCm39)	missense	probably benign	0.25
R5049:Vmn1r184	UTSW	7	25,966,793 (GRCm39)	missense	possibly damaging	0.49
R5076:Vmn1r184	UTSW	7	25,966,346 (GRCm39)	missense	probably benign	0.00
R5213:Vmn1r184	UTSW	7	25,967,136 (GRCm39)	missense	probably damaging	0.99
R5554:Vmn1r184	UTSW	7	25,966,413 (GRCm39)	missense	probably damaging	1.00
R6146:Vmn1r184	UTSW	7	25,966,817 (GRCm39)	missense	probably benign	0.08
R6937:Vmn1r184	UTSW	7	25,966,750 (GRCm39)	missense	probably benign	0.08
R6943:Vmn1r184	UTSW	7	25,966,563 (GRCm39)	missense	possibly damaging	0.77
R7190:Vmn1r184	UTSW	7	25,967,105 (GRCm39)	missense	probably damaging	1.00
R7239:Vmn1r184	UTSW	7	25,966,602 (GRCm39)	missense	possibly damaging	0.79
R7472:Vmn1r184	UTSW	7	25,966,824 (GRCm39)	missense	possibly damaging	0.82
R8258:Vmn1r184	UTSW	7	25,966,686 (GRCm39)	missense	probably benign	0.44
R8259:Vmn1r184	UTSW	7	25,966,686 (GRCm39)	missense	probably benign	0.44
R8911:Vmn1r184	UTSW	7	25,966,310 (GRCm39)	missense	possibly damaging	0.89
R9008:Vmn1r184	UTSW	7	25,967,177 (GRCm39)	missense	probably benign
R9159:Vmn1r184	UTSW	7	25,966,545 (GRCm39)	missense	possibly damaging	0.65
R9216:Vmn1r184	UTSW	7	25,966,703 (GRCm39)	missense	probably benign	0.00
R9548:Vmn1r184	UTSW	7	25,966,734 (GRCm39)	missense	probably benign	0.29
R9588:Vmn1r184	UTSW	7	25,966,347 (GRCm39)	missense	probably null	0.78
Z1177:Vmn1r184	UTSW	7	25,966,415 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- GACCACTTGCCTCTTGAGTG -3'
(R):5'- GGACACCAGAGCCAGAATGTTC -3'

Sequencing Primer
(F):5'- GAGTGTTTTTCAGGCCATGACCATC -3'
(R):5'- CTATGGATGTGTAGAACCCTCTGC -3'

Posted On

2018-10-18