Mutagenetix > Incidental Mutation

Incidental Mutation 'R1055:Vmn2r32'

94267

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r32

Ensembl Gene

ENSMUSG00000096743

Gene Name

vomeronasal 2, receptor 32

Synonyms

V2r5

MMRRC Submission

039145-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.249) question?

Stock #

R1055 (G1)

Quality Score

Status

Not validated

Chromosome

Chromosomal Location

7466968-7482972 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 7477326 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Stop codon at position 355 (W355*)

Ref Sequence

ENSEMBL: ENSMUSP00000092462 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094866]

AlphaFold

K7N686

Predicted Effect

probably null
Transcript: ENSMUST00000094866
AA Change: W355*

SMART Domains

Protein: ENSMUSP00000092462
Gene: ENSMUSG00000096743
AA Change: W355*

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	73	470	3.6e-33	PFAM
Pfam:NCD3G	512	565	8.1e-21	PFAM
Pfam:7tm_3	598	833	9.5e-55	PFAM

Coding Region Coverage

1x: 99.4%
3x: 98.3%
10x: 95.3%
20x: 87.5%

Validation Efficiency

100% (58/58)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930578I06Rik	A	G	14: 64,210,724 (GRCm39)	V168A	possibly damaging	Het
A1cf	C	A	19: 31,909,919 (GRCm39)	T237N	probably benign	Het
Actl10	A	T	2: 154,394,588 (GRCm39)	Q180L	probably benign	Het
Adcy1	T	C	11: 7,059,075 (GRCm39)	L327P	probably damaging	Het
Adcy7	T	C	8: 89,044,685 (GRCm39)		probably benign	Het
Ahctf1	G	A	1: 179,591,051 (GRCm39)	T1243I	possibly damaging	Het
Akap6	C	T	12: 52,927,455 (GRCm39)	Q122*	probably null	Het
Apob	G	A	12: 8,044,963 (GRCm39)	G861D	probably damaging	Het
Arhgef11	A	C	3: 87,624,425 (GRCm39)	T539P	probably benign	Het
Cd244a	T	A	1: 171,404,844 (GRCm39)	V232E	probably damaging	Het
Chia1	A	C	3: 106,038,199 (GRCm39)	D365A	probably damaging	Het
Clpsl2	C	T	17: 28,768,500 (GRCm39)	Q5*	probably null	Het
Clrn1	T	A	3: 58,772,531 (GRCm39)	I117F	probably benign	Het
Csmd3	A	G	15: 47,744,933 (GRCm39)	L1354P	probably damaging	Het
Csn2	G	A	5: 87,842,596 (GRCm39)	P144S	possibly damaging	Het
Dcdc2a	T	A	13: 25,286,593 (GRCm39)	M172K	probably damaging	Het
Dnah9	A	T	11: 66,050,837 (GRCm39)	W152R	probably damaging	Het
Dnmt3a	T	A	12: 3,922,864 (GRCm39)	S82T	probably benign	Het
Ebf1	A	G	11: 44,523,602 (GRCm39)	K146E	probably damaging	Het
Gfpt2	A	C	11: 49,718,038 (GRCm39)	R504S	probably damaging	Het
Gpank1	T	A	17: 35,343,284 (GRCm39)	S255T	probably damaging	Het
Greb1	T	C	12: 16,732,252 (GRCm39)	M1570V	probably damaging	Het
Gtf2i	A	T	5: 134,292,478 (GRCm39)	I403K	probably damaging	Het
Hoxc11	T	A	15: 102,863,270 (GRCm39)	C104S	probably damaging	Het
Hsh2d	G	A	8: 72,954,304 (GRCm39)	D229N	probably benign	Het
Ilrun	T	C	17: 27,986,910 (GRCm39)	N272S	probably damaging	Het
Khdrbs2	A	T	1: 32,683,238 (GRCm39)		probably benign	Het
Lix1l	G	T	3: 96,528,626 (GRCm39)	G200V	probably damaging	Het
Lrrc23	T	C	6: 124,755,114 (GRCm39)	N141S	probably damaging	Het
Marchf11	A	T	15: 26,309,748 (GRCm39)	D134V	probably damaging	Het
Myo9a	A	T	9: 59,762,653 (GRCm39)	T795S	probably benign	Het
Nhsl1	T	A	10: 18,401,223 (GRCm39)	D782E	probably benign	Het
Nptxr	T	C	15: 79,674,456 (GRCm39)		probably benign	Het
Nrp1	A	G	8: 129,195,079 (GRCm39)	M512V	possibly damaging	Het
Ofcc1	C	T	13: 40,362,305 (GRCm39)	G206R	probably benign	Het
Or12e7	ATTGCTACTC	A	2: 87,287,781 (GRCm39)		probably benign	Het
Or5b3	G	A	19: 13,388,754 (GRCm39)	A274T	probably benign	Het
Pard3	T	C	8: 128,104,761 (GRCm39)	F267S	probably benign	Het
Pomt2	G	A	12: 87,194,254 (GRCm39)	T50M	possibly damaging	Het
Qsox2	A	G	2: 26,104,137 (GRCm39)	Y298H	probably damaging	Het
Rabgap1	A	G	2: 37,382,080 (GRCm39)	K450E	possibly damaging	Het
Rpa1	A	T	11: 75,193,558 (GRCm39)	V591D	probably damaging	Het
Sall3	A	C	18: 81,013,007 (GRCm39)	M1143R	probably benign	Het
Scgb1b19	G	T	7: 32,986,768 (GRCm39)	A13S	unknown	Het
Scn1a	T	C	2: 66,168,340 (GRCm39)	T89A	probably benign	Het
Sdk2	C	T	11: 113,729,472 (GRCm39)		silent	Het
Sdr42e1	T	G	8: 118,390,323 (GRCm39)	N106T	probably damaging	Het
Shpk	A	T	11: 73,105,945 (GRCm39)	M266L	probably benign	Het
Slc34a1	G	T	13: 55,550,846 (GRCm39)	R139L	probably benign	Het
Smbd1	C	A	16: 32,627,088 (GRCm39)	D67Y	probably damaging	Het
Srd5a3	A	G	5: 76,301,485 (GRCm39)	N238S	probably benign	Het
Tmprss2	T	C	16: 97,377,462 (GRCm39)	N212D	probably damaging	Het
Uap1	G	T	1: 169,984,480 (GRCm39)		probably benign	Het
Ugt1a6a	A	G	1: 88,066,736 (GRCm39)	M181V	probably benign	Het
Vmn2r86	T	A	10: 130,282,226 (GRCm39)	S797C	probably damaging	Het
Wiz	A	G	17: 32,606,616 (GRCm39)	S40P	probably damaging	Het
Zfand6	A	G	7: 84,265,181 (GRCm39)		probably benign	Het
Zfp280d	G	A	9: 72,236,449 (GRCm39)		probably null	Het

Other mutations in Vmn2r32

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02140:Vmn2r32	APN	7	7,479,696 (GRCm39)	missense	probably damaging	0.97
IGL02333:Vmn2r32	APN	7	7,467,143 (GRCm39)	missense	probably damaging	1.00
IGL02406:Vmn2r32	APN	7	7,479,709 (GRCm39)	missense	probably benign
IGL02428:Vmn2r32	APN	7	7,477,283 (GRCm39)	missense	probably benign	0.02
IGL02484:Vmn2r32	APN	7	7,467,116 (GRCm39)	missense	probably damaging	1.00
IGL03277:Vmn2r32	APN	7	7,477,251 (GRCm39)	missense	probably benign	0.23
IGL03366:Vmn2r32	APN	7	7,467,029 (GRCm39)	missense	probably damaging	0.99
R1695:Vmn2r32	UTSW	7	7,466,991 (GRCm39)	missense	probably benign	0.01
R2172:Vmn2r32	UTSW	7	7,477,614 (GRCm39)	missense	probably damaging	0.99
R2262:Vmn2r32	UTSW	7	7,477,618 (GRCm39)	missense	probably benign
R3150:Vmn2r32	UTSW	7	7,475,554 (GRCm39)	missense	probably benign
R4362:Vmn2r32	UTSW	7	7,482,857 (GRCm39)	nonsense	probably null
R4432:Vmn2r32	UTSW	7	7,482,918 (GRCm39)	missense	probably damaging	0.98
R4851:Vmn2r32	UTSW	7	7,482,953 (GRCm39)	missense	possibly damaging	0.59
R4949:Vmn2r32	UTSW	7	7,467,083 (GRCm39)	missense	probably benign	0.22
R5990:Vmn2r32	UTSW	7	7,482,809 (GRCm39)	missense	probably damaging	0.97
R6083:Vmn2r32	UTSW	7	7,467,209 (GRCm39)	missense	probably benign	0.15
R6084:Vmn2r32	UTSW	7	7,467,209 (GRCm39)	missense	probably benign	0.15
R6116:Vmn2r32	UTSW	7	7,467,092 (GRCm39)	missense	probably damaging	1.00
R6263:Vmn2r32	UTSW	7	7,479,691 (GRCm39)	missense	possibly damaging	0.90
R6889:Vmn2r32	UTSW	7	7,475,573 (GRCm39)	missense	possibly damaging	0.82
R7286:Vmn2r32	UTSW	7	7,482,807 (GRCm39)	missense	probably benign	0.21
R7390:Vmn2r32	UTSW	7	7,482,851 (GRCm39)	missense	probably benign	0.00
R7412:Vmn2r32	UTSW	7	7,477,212 (GRCm39)	missense	possibly damaging	0.53
R7508:Vmn2r32	UTSW	7	7,470,373 (GRCm39)	missense	possibly damaging	0.87
R8812:Vmn2r32	UTSW	7	7,477,669 (GRCm39)	missense	probably damaging	1.00
R8968:Vmn2r32	UTSW	7	7,477,204 (GRCm39)	missense	probably benign	0.00
R9331:Vmn2r32	UTSW	7	7,467,402 (GRCm39)	nonsense	probably null
R9358:Vmn2r32	UTSW	7	7,477,197 (GRCm39)	missense	probably damaging	1.00
Z1177:Vmn2r32	UTSW	7	7,477,160 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- CTTCAAGCAGTGAGAACTGGCTCC -3'
(R):5'- TCTCTATCAGATGGCCCCAAAGGAC -3'

Sequencing Primer
(F):5'- GATTATCAGCCTGTTGCAGATTC -3'
(R):5'- TTCAGAATGTGGGAACCTCC -3'

Posted On

2014-01-05