Mutagenetix > Incidental Mutations

Incidental Mutation 'R3552:Vmn1r38'

268989

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r38

Ensembl Gene

ENSMUSG00000115170

Gene Name

vomeronasal 1 receptor 38

Synonyms

V1rc13

MMRRC Submission

040669-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.252) question?

Stock #

R3552 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

66774003-66782627 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 66776493 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 213 (H213R)

Ref Sequence

ENSEMBL: ENSMUSP00000154495 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000176121] [ENSMUST00000226457] [ENSMUST00000227493] [ENSMUST00000227694]

AlphaFold

Q8R2E1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000176121
AA Change: H213R

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000135117
Gene: ENSMUSG00000093632
AA Change: H213R

Domain	Start	End	E-Value	Type
Pfam:V1R	28	293	3.7e-53	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000226457
AA Change: H213R

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000227493
AA Change: H213R

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000227694
AA Change: H213R

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.5%
10x: 96.8%
20x: 93.4%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610009O20Rik	A	G	18: 38,258,365		probably benign	Het
Acaca	T	A	11: 84,261,624	Y866N	probably damaging	Het
Agk	A	G	6: 40,394,681	T371A	probably benign	Het
Akna	T	C	4: 63,398,124	M1V	probably null	Het
Aldh7a1	T	C	18: 56,550,292		probably null	Het
Ankrd26	A	T	6: 118,507,776	L1500H	probably damaging	Het
Atp13a5	T	A	16: 29,310,766	D452V	probably damaging	Het
Bahcc1	C	T	11: 120,276,772	T1333M	possibly damaging	Het
Carmil3	G	T	14: 55,507,402	R1276L	possibly damaging	Het
Ccni	T	C	5: 93,187,761	S173G	probably benign	Het
Chrm2	A	T	6: 36,523,810	I201F	probably damaging	Het
Col16a1	A	G	4: 130,077,041	T618A	probably benign	Het
Dock2	T	C	11: 34,720,960	Y192C	probably benign	Het
Ep400	T	A	5: 110,729,287	E821V	unknown	Het
Esrrg	G	A	1: 188,150,190	V215I	probably benign	Het
Evx1	A	T	6: 52,316,923	S359C	probably damaging	Het
Fcrls	A	G	3: 87,259,410	I92T	possibly damaging	Het
Gal3st1	T	A	11: 3,998,110	F106I	possibly damaging	Het
Gm9944	T	C	4: 144,453,043		probably benign	Het
Hjurp	GT	GTT	1: 88,266,524		probably null	Het
Hrc	G	C	7: 45,336,333	E303Q	possibly damaging	Het
Kcnh1	A	G	1: 192,238,766	N118D	probably damaging	Het
Khdrbs1	A	G	4: 129,720,791	I323T	possibly damaging	Het
Klhdc7b	T	C	15: 89,387,521	Y869H	probably benign	Het
Lrrc4c	T	A	2: 97,629,961	W311R	probably damaging	Het
Megf11	A	G	9: 64,695,463	D862G	possibly damaging	Het
Muc5b	A	G	7: 141,861,335	T2673A	possibly damaging	Het
Muc5b	A	G	7: 141,867,705	S4311G	probably benign	Het
Myo15	C	T	11: 60,509,663	A1767V	possibly damaging	Het
Neo1	T	A	9: 58,893,878	K1140M	probably damaging	Het
Oc90	T	C	15: 65,878,801	Q365R	possibly damaging	Het
Olfr1012	T	C	2: 85,759,893	N161S	possibly damaging	Het
Olfr378	T	C	11: 73,425,852	I44V	probably benign	Het
Olfr48	A	C	2: 89,844,343	M210R	possibly damaging	Het
Oplah	C	T	15: 76,302,094	D734N	possibly damaging	Het
Pbx1	G	A	1: 168,158,793	P411L	possibly damaging	Het
Pcdhga6	G	T	18: 37,708,217	R330L	probably benign	Het
Phox2b	C	A	5: 67,097,656	R150L	probably damaging	Het
Plscr2	A	G	9: 92,290,795	E169G	probably damaging	Het
Ptprn2	A	T	12: 116,888,877	Q518L	probably benign	Het
Rbl1	A	T	2: 157,195,585	I214K	probably benign	Het
Ryr1	T	A	7: 29,056,997	Q3464L	probably damaging	Het
Ryr3	T	A	2: 112,751,787	I2854F	probably damaging	Het
Shtn1	T	C	19: 58,975,038	Y615C	probably benign	Het
Sirt5	A	T	13: 43,383,167	N226Y	probably damaging	Het
Slc30a3	G	A	5: 31,095,078		probably benign	Het
Slc5a4b	A	G	10: 76,081,524	V226A	probably damaging	Het
Slf2	C	A	19: 44,934,951	S68*	probably null	Het
Smyd5	G	A	6: 85,442,211	E292K	probably damaging	Het
Spns1	A	G	7: 126,370,371	V512A	possibly damaging	Het
Sry	T	A	Y: 2,663,141	Q173L	unknown	Het
Ssrp1	C	A	2: 85,044,392	Q519K	probably benign	Het
Tgfbr3	T	C	5: 107,139,839	E498G	probably damaging	Het
Tnrc6b	T	G	15: 80,880,247	L650W	probably damaging	Het
Tnxb	A	T	17: 34,718,721	E3861D	probably damaging	Het
Trbc1	G	T	6: 41,539,645		probably benign	Het
Trpm7	T	A	2: 126,826,710		probably benign	Het
Usp39	G	A	6: 72,337,832	T197I	possibly damaging	Het
Washc2	A	G	6: 116,220,568	D168G	probably damaging	Het
Washc4	A	G	10: 83,546,856	I45V	probably benign	Het
Zfp352	A	G	4: 90,225,102	E493G	probably benign	Het
Zfp692	C	T	11: 58,309,428	T170I	possibly damaging	Het
Zfp735	C	A	11: 73,711,241	S337*	probably null	Het

Other mutations in Vmn1r38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01892:Vmn1r38	APN	6	66776376	missense	probably benign	0.00
IGL02471:Vmn1r38	APN	6	66776767	missense	probably benign	0.06
R0483:Vmn1r38	UTSW	6	66776995	missense	probably benign	0.10
R0890:Vmn1r38	UTSW	6	66776530	missense	probably benign	0.01
R1242:Vmn1r38	UTSW	6	66776360	nonsense	probably null
R1557:Vmn1r38	UTSW	6	66776386	missense	probably benign	0.01
R2266:Vmn1r38	UTSW	6	66776449	missense	probably benign	0.02
R2320:Vmn1r38	UTSW	6	66776550	missense	possibly damaging	0.94
R2568:Vmn1r38	UTSW	6	66776971	missense	probably benign	0.00
R3104:Vmn1r38	UTSW	6	66776446	missense	probably benign	0.31
R3792:Vmn1r38	UTSW	6	66776907	missense	probably benign	0.01
R4061:Vmn1r38	UTSW	6	66776848	missense	possibly damaging	0.87
R4532:Vmn1r38	UTSW	6	66777032	missense	probably benign	0.38
R5299:Vmn1r38	UTSW	6	66776698	missense	probably benign	0.06
R7173:Vmn1r38	UTSW	6	66776294	missense	possibly damaging	0.88
R8044:Vmn1r38	UTSW	6	66776532	missense	probably benign	0.12
R8935:Vmn1r38	UTSW	6	66776995	missense	probably benign	0.12
R9144:Vmn1r38	UTSW	6	66776628	missense	probably benign	0.21
X0022:Vmn1r38	UTSW	6	66777067	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGTAATTGTGGGATAGGCATTCAAC -3'
(R):5'- CTATACTGGTGCTTATATCAACGTG -3'

Sequencing Primer
(F):5'- GGATAGGCATTCAACACAAACTTCTG -3'
(R):5'- CGTGAGTGAGACCAACCAG -3'

Posted On

2015-02-19