Mutagenetix > Incidental Mutation

Incidental Mutation 'R6610:Vmn2r31'

525887

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r31

Ensembl Gene

ENSMUSG00000096373

Gene Name

vomeronasal 2, receptor 31

Synonyms

MMRRC Submission

044733-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.190) question?

Stock #

R6610 (G1)

Quality Score

141.008

Status

Not validated

Chromosome

Chromosomal Location

7386984-7402626 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 7387588 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 661 (V661E)

Ref Sequence

ENSEMBL: ENSMUSP00000074613 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075108]

AlphaFold

L7N1Z4

Predicted Effect

probably damaging
Transcript: ENSMUST00000075108
AA Change: V661E

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000074613
Gene: ENSMUSG00000096373
AA Change: V661E

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	73	469	1e-33	PFAM
Pfam:NCD3G	512	565	1.4e-20	PFAM
Pfam:7tm_3	598	833	8.1e-55	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.9%
20x: 93.8%

Validation Efficiency

100% (42/42)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AB124611	A	T	9: 21,437,561 (GRCm39)	M1L	probably benign	Het
Adam26b	T	C	8: 43,974,190 (GRCm39)	K271E	probably damaging	Het
Ankrd44	A	G	1: 54,694,246 (GRCm39)	I914T	probably benign	Het
Atp12a	A	G	14: 56,612,013 (GRCm39)	R396G	probably damaging	Het
C2cd3	A	G	7: 100,104,505 (GRCm39)	K2173E	probably benign	Het
Cbx2	A	G	11: 118,915,036 (GRCm39)	D51G	probably damaging	Het
Ccdc33	T	A	9: 57,976,419 (GRCm39)	T532S	possibly damaging	Het
Ccnt1	T	C	15: 98,462,982 (GRCm39)	I63M	probably damaging	Het
Cdc20b	C	T	13: 113,200,796 (GRCm39)	T172I	probably benign	Het
Cep20	TTGTG	TTG	16: 14,118,009 (GRCm39)		probably null	Het
Ces2f	T	G	8: 105,676,738 (GRCm39)		probably null	Het
Cfh	A	T	1: 140,029,486 (GRCm39)	C597*	probably null	Het
Cntnap2	A	T	6: 45,992,191 (GRCm39)	T373S	probably benign	Het
Cyb5r4	T	G	9: 86,941,470 (GRCm39)	C64G	probably benign	Het
Cyp2c23	A	G	19: 43,995,520 (GRCm39)	F416L	probably damaging	Het
Dnah8	G	A	17: 30,967,542 (GRCm39)	D2585N	probably benign	Het
Eif4e1b	A	G	13: 54,932,128 (GRCm39)		probably benign	Het
Elp1	A	G	4: 56,758,236 (GRCm39)	V1227A	probably benign	Het
Etl4	G	A	2: 20,718,180 (GRCm39)	R256K	probably damaging	Het
Fhad1	A	G	4: 141,643,707 (GRCm39)	L1054P	possibly damaging	Het
Grik1	A	G	16: 87,831,200 (GRCm39)	I190T	probably damaging	Het
Gsdmc2	T	C	15: 63,696,857 (GRCm39)	N438S	probably benign	Het
Igkv15-103	A	T	6: 68,414,617 (GRCm39)	R19*	probably null	Het
Kcnc2	G	C	10: 112,107,761 (GRCm39)	G51R	probably benign	Het
Lhcgr	A	T	17: 89,077,307 (GRCm39)	I93K	possibly damaging	Het
Muc6	G	C	7: 141,226,700 (GRCm39)		probably benign	Het
Mymk	G	T	2: 26,957,405 (GRCm39)	S29R	possibly damaging	Het
Nab2	A	T	10: 127,500,207 (GRCm39)	I295N	probably damaging	Het
Neu2	A	T	1: 87,524,407 (GRCm39)	T131S	probably benign	Het
Pdcd7	T	A	9: 65,261,965 (GRCm39)	M129K	possibly damaging	Het
Ptar1	A	G	19: 23,695,208 (GRCm39)	H225R	probably benign	Het
Pygb	T	A	2: 150,665,886 (GRCm39)		probably null	Het
Rpap3	T	C	15: 97,586,049 (GRCm39)	D314G	probably benign	Het
Scara3	A	G	14: 66,168,670 (GRCm39)	S316P	probably damaging	Het
Sec24a	C	T	11: 51,587,483 (GRCm39)	V1051I	probably benign	Het
Setdb1	G	T	3: 95,235,888 (GRCm39)	A841D	probably damaging	Het
Stk32b	G	A	5: 37,606,022 (GRCm39)	T407I	probably benign	Het
Tcte2	G	A	17: 13,948,250 (GRCm39)	Q10*	probably null	Het
Tgm2	C	A	2: 157,985,020 (GRCm39)	E29*	probably null	Het
Trim32	G	A	4: 65,533,308 (GRCm39)	V622M	probably damaging	Het
Ttn	G	A	2: 76,579,673 (GRCm39)	T23740M	probably damaging	Het
Tyk2	G	T	9: 21,019,312 (GRCm39)	Q1014K	probably benign	Het
Vmn1r123	A	G	7: 20,896,515 (GRCm39)	N136D	probably benign	Het
Vmn2r85	A	T	10: 130,261,838 (GRCm39)	F166L	probably damaging	Het
Zfp426	T	C	9: 20,384,389 (GRCm39)	K98R	probably damaging	Het
Zfp534	C	T	4: 147,758,947 (GRCm39)	R574K	probably benign	Het

Other mutations in Vmn2r31

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01104:Vmn2r31	APN	7	7,399,565 (GRCm39)	missense	probably damaging	0.98
IGL01536:Vmn2r31	APN	7	7,387,847 (GRCm39)	missense	probably damaging	1.00
IGL01985:Vmn2r31	APN	7	7,397,510 (GRCm39)	missense	probably benign
IGL02116:Vmn2r31	APN	7	7,397,548 (GRCm39)	missense	probably damaging	0.97
FR4304:Vmn2r31	UTSW	7	7,387,607 (GRCm39)	missense	probably damaging	1.00
R1609:Vmn2r31	UTSW	7	7,387,888 (GRCm39)	missense	probably damaging	1.00
R4647:Vmn2r31	UTSW	7	7,387,367 (GRCm39)	missense	probably damaging	1.00
R4724:Vmn2r31	UTSW	7	7,387,757 (GRCm39)	missense	possibly damaging	0.63
R4824:Vmn2r31	UTSW	7	7,390,062 (GRCm39)	critical splice donor site	probably null
R5619:Vmn2r31	UTSW	7	7,387,529 (GRCm39)	nonsense	probably null
R6225:Vmn2r31	UTSW	7	7,397,638 (GRCm39)	missense	probably benign	0.19
R6956:Vmn2r31	UTSW	7	7,397,505 (GRCm39)	missense	probably benign
R7111:Vmn2r31	UTSW	7	7,399,480 (GRCm39)	missense	probably damaging	0.99
R7219:Vmn2r31	UTSW	7	7,397,397 (GRCm39)	missense	probably damaging	0.97
R7219:Vmn2r31	UTSW	7	7,390,105 (GRCm39)	missense	probably benign
R7300:Vmn2r31	UTSW	7	7,387,775 (GRCm39)	missense	possibly damaging	0.61
R7395:Vmn2r31	UTSW	7	7,387,744 (GRCm39)	missense	probably damaging	1.00
R7481:Vmn2r31	UTSW	7	7,387,579 (GRCm39)	missense	possibly damaging	0.94
R8015:Vmn2r31	UTSW	7	7,387,199 (GRCm39)	missense	probably damaging	1.00
R8434:Vmn2r31	UTSW	7	7,387,699 (GRCm39)	missense	probably damaging	1.00
R8781:Vmn2r31	UTSW	7	7,387,400 (GRCm39)	missense	possibly damaging	0.65
R8972:Vmn2r31	UTSW	7	7,399,654 (GRCm39)	missense	probably benign	0.00
R9034:Vmn2r31	UTSW	7	7,397,680 (GRCm39)	missense	probably benign	0.08
R9596:Vmn2r31	UTSW	7	7,397,292 (GRCm39)	missense	probably benign	0.01
R9711:Vmn2r31	UTSW	7	7,387,085 (GRCm39)	missense	probably damaging	0.99
R9714:Vmn2r31	UTSW	7	7,387,367 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCATGCTGAGAGTGTTCATC -3'
(R):5'- TCTGCATTCACAGCTGTGG -3'

Sequencing Primer
(F):5'- CCATGCTGAGAGTGTTCATCAATATC -3'
(R):5'- CATTCACAGCTGTGGTACTTTG -3'

Posted On

2018-06-22