Mutagenetix > Incidental Mutation

Incidental Mutation 'R0812:Vmn2r75'

78475

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r75

Ensembl Gene

ENSMUSG00000090436

Gene Name

vomeronasal 2, receptor 75

Synonyms

EG546981

MMRRC Submission

038992-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R0812 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

86148042-86171724 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 86165367 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Glutamic Acid at position 306 (G306E)

Ref Sequence

ENSEMBL: ENSMUSP00000126973 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000167830]

AlphaFold

G5E8Z7

Predicted Effect

probably benign
Transcript: ENSMUST00000167830
AA Change: G306E

PolyPhen 2 Score 0.378 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000126973
Gene: ENSMUSG00000090436
AA Change: G306E

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Pfam:ANF_receptor	80	466	2.8e-31	PFAM
Pfam:NCD3G	510	562	4.6e-20	PFAM
Pfam:7tm_3	593	829	7.7e-51	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.6%
3x: 98.9%
10x: 96.8%
20x: 91.7%

Validation Efficiency

96% (52/54)

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930402H24Rik	A	G	2: 130,713,414 (GRCm38)	F858S	probably damaging	Het
Abcb1a	T	C	5: 8,713,229 (GRCm38)	S586P	probably damaging	Het
Abcc3	G	A	11: 94,375,202 (GRCm38)		probably benign	Het
Ap5z1	G	A	5: 142,475,791 (GRCm38)	R583H	probably benign	Het
Arrb1	G	T	7: 99,598,501 (GRCm38)	V346L	probably benign	Het
Atrnl1	T	A	19: 57,673,141 (GRCm38)	F518I	probably benign	Het
Bank1	T	A	3: 136,093,366 (GRCm38)	I405F	probably damaging	Het
Cacna1c	A	G	6: 118,630,263 (GRCm38)	C1227R	probably benign	Het
Cacna1h	A	G	17: 25,388,628 (GRCm38)	L905P	probably damaging	Het
Cc2d1a	A	G	8: 84,133,836 (GRCm38)	Y826H	probably benign	Het
Cenpo	A	G	12: 4,216,643 (GRCm38)	V155A	probably benign	Het
Cnmd	A	G	14: 79,661,423 (GRCm38)	F63S	probably damaging	Het
Cnn3	G	A	3: 121,454,951 (GRCm38)	G72D	probably damaging	Het
Cox10	A	G	11: 64,071,713 (GRCm38)	S101P	probably benign	Het
Ctdsp1	T	C	1: 74,394,647 (GRCm38)	V129A	probably damaging	Het
Cyp2d34	A	T	15: 82,618,606 (GRCm38)	S140T	probably benign	Het
Dennd5a	G	A	7: 109,933,613 (GRCm38)	H317Y	possibly damaging	Het
Eef2	C	CN	10: 81,178,769 (GRCm38)		probably null	Het
Enox1	T	A	14: 77,582,436 (GRCm38)	D210E	probably damaging	Het
Fam171a1	A	G	2: 3,197,427 (GRCm38)	N190S	probably damaging	Het
Fat2	T	A	11: 55,253,633 (GRCm38)	K4138N	possibly damaging	Het
Fat4	A	T	3: 38,957,474 (GRCm38)	D2241V	probably damaging	Het
Fbn1	C	T	2: 125,403,170 (GRCm38)	V266I	possibly damaging	Het
Foxf2	T	A	13: 31,627,205 (GRCm38)	Y376N	probably damaging	Het
Fras1	T	A	5: 96,752,998 (GRCm38)	S3025R	probably benign	Het
Gba	T	C	3: 89,204,000 (GRCm38)	I24T	probably benign	Het
Gdpd5	A	G	7: 99,438,333 (GRCm38)	D68G	probably damaging	Het
Grid1	G	A	14: 34,822,619 (GRCm38)	S49N	probably benign	Het
Grtp1	T	C	8: 13,179,639 (GRCm38)	T250A	possibly damaging	Het
Gucy1b1	T	C	3: 82,037,988 (GRCm38)	N448D	probably benign	Het
H2-Ob	A	G	17: 34,244,126 (GRCm38)		probably benign	Het
Hcn4	A	G	9: 58,823,512 (GRCm38)	M1V	probably null	Het
Hmcn2	G	A	2: 31,420,371 (GRCm38)	A3326T	probably damaging	Het
Impg2	TACCACCACCACCACCACCACCACCA	TACCACCACCACCACCACCACCA	16: 56,257,939 (GRCm38)		probably benign	Het
Ippk	C	A	13: 49,443,471 (GRCm38)	Q254K	probably damaging	Het
Itga2	A	T	13: 114,870,614 (GRCm38)	L393I	possibly damaging	Het
Kcna10	A	T	3: 107,195,259 (GRCm38)	E402V	possibly damaging	Het
Kcnab1	G	A	3: 65,297,720 (GRCm38)	D119N	probably damaging	Het
Kcnip4	T	A	5: 48,409,860 (GRCm38)	T122S	probably benign	Het
Kcnma1	G	A	14: 23,300,018 (GRCm38)	P1151L	probably damaging	Het
Klhl22	T	A	16: 17,792,589 (GRCm38)	M568K	probably benign	Het
Krt6a	C	T	15: 101,692,748 (GRCm38)	V257M	probably damaging	Het
Ksr2	A	C	5: 117,555,225 (GRCm38)	H246P	probably damaging	Het
Lca5	T	C	9: 83,399,753 (GRCm38)	D326G	possibly damaging	Het
Lcp1	A	G	14: 75,214,488 (GRCm38)	E393G	probably benign	Het
Leo1	G	A	9: 75,445,549 (GRCm38)	E125K	probably benign	Het
Lipt1	T	A	1: 37,875,301 (GRCm38)	V146E	probably damaging	Het
Mael	A	T	1: 166,235,399 (GRCm38)		probably null	Het
Mga	C	T	2: 119,947,961 (GRCm38)	L1996F	probably damaging	Het
Mllt6	A	G	11: 97,678,561 (GRCm38)	N913S	probably damaging	Het
Mphosph9	A	C	5: 124,298,759 (GRCm38)	D507E	probably damaging	Het
Mvp	G	A	7: 126,987,556 (GRCm38)	A801V	probably benign	Het
Ndrg2	A	G	14: 51,908,662 (GRCm38)		probably benign	Het
Neb	T	C	2: 52,292,695 (GRCm38)	D1053G	possibly damaging	Het
Nubp1	C	A	16: 10,413,721 (GRCm38)	L79I	probably benign	Het
Olfr397	G	A	11: 73,965,420 (GRCm38)	E271K	probably benign	Het
Olfr924	G	A	9: 38,848,509 (GRCm38)	V132I	probably benign	Het
Olfr97	A	C	17: 37,232,332 (GRCm38)	L13V	probably benign	Het
Pnpla8	G	A	12: 44,283,405 (GRCm38)	V29M	probably benign	Het
Psmb2	T	A	4: 126,707,557 (GRCm38)	I151N	possibly damaging	Het
Ptgs2	C	T	1: 150,101,354 (GRCm38)	T104I	probably benign	Het
Ptpro	A	G	6: 137,368,079 (GRCm38)	T28A	probably benign	Het
Raf1	A	G	6: 115,626,710 (GRCm38)		probably null	Het
Ranbp2	T	C	10: 58,465,529 (GRCm38)	M668T	probably benign	Het
Rbm48	A	T	5: 3,591,760 (GRCm38)		probably null	Het
Rhag	A	T	17: 40,831,578 (GRCm38)	T225S	possibly damaging	Het
Rhof	A	C	5: 123,131,887 (GRCm38)	L69R	probably damaging	Het
Slc24a5	T	C	2: 125,068,804 (GRCm38)	S52P	probably damaging	Het
Slc8a2	T	C	7: 16,141,114 (GRCm38)	V429A	probably damaging	Het
Slfn10-ps	G	A	11: 83,035,562 (GRCm38)		noncoding transcript	Het
Spam1	G	A	6: 24,796,887 (GRCm38)	R279H	probably damaging	Het
Srfbp1	A	G	18: 52,487,516 (GRCm38)	D102G	probably damaging	Het
Srrm3	A	C	5: 135,873,282 (GRCm38)		probably benign	Het
Tk1	T	C	11: 117,822,107 (GRCm38)	E98G	probably damaging	Het
Trim13	G	A	14: 61,605,700 (GRCm38)	V389I	probably benign	Het
Ttc28	A	T	5: 111,235,500 (GRCm38)	Y1289F	probably benign	Het
Ugcg	C	T	4: 59,207,798 (GRCm38)	P46S	probably benign	Het
Ugt1a10	T	A	1: 88,056,182 (GRCm38)	V234D	probably benign	Het
Vmn2r18	C	A	5: 151,572,930 (GRCm38)		probably benign	Het
Vmn2r86	C	T	10: 130,453,628 (GRCm38)	V133I	probably benign	Het
Vps13c	C	A	9: 67,934,476 (GRCm38)	Q1927K	probably benign	Het
Zbtb14	C	A	17: 69,388,502 (GRCm38)	F398L	probably damaging	Het
Zfp219	T	A	14: 52,006,938 (GRCm38)	T550S	probably benign	Het
Zfp329	T	A	7: 12,811,468 (GRCm38)	N43I	probably benign	Het
Zfp507	G	A	7: 35,802,623 (GRCm38)		probably benign	Het
Zfp97	T	A	17: 17,145,290 (GRCm38)	F350L	possibly damaging	Het

Other mutations in Vmn2r75

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01133:Vmn2r75	APN	7	86,148,032 (GRCm38)	unclassified	probably benign
IGL01287:Vmn2r75	APN	7	86,148,593 (GRCm38)	missense	probably damaging	0.97
IGL01318:Vmn2r75	APN	7	86,165,566 (GRCm38)	missense	probably benign	0.06
IGL01331:Vmn2r75	APN	7	86,171,662 (GRCm38)	nonsense	probably null
IGL01406:Vmn2r75	APN	7	86,163,292 (GRCm38)	splice site	probably benign
IGL01615:Vmn2r75	APN	7	86,148,473 (GRCm38)	missense	probably benign	0.03
IGL01657:Vmn2r75	APN	7	86,164,247 (GRCm38)	missense	probably damaging	1.00
IGL02237:Vmn2r75	APN	7	86,165,578 (GRCm38)	missense	possibly damaging	0.88
IGL02275:Vmn2r75	APN	7	86,165,140 (GRCm38)	missense	probably benign	0.04
IGL02307:Vmn2r75	APN	7	86,165,766 (GRCm38)	missense	probably benign	0.00
IGL03136:Vmn2r75	APN	7	86,148,703 (GRCm38)	missense	possibly damaging	0.89
IGL03160:Vmn2r75	APN	7	86,148,436 (GRCm38)	missense	probably damaging	1.00
IGL03244:Vmn2r75	APN	7	86,171,725 (GRCm38)	unclassified	probably benign
PIT4449001:Vmn2r75	UTSW	7	86,165,583 (GRCm38)	missense	probably damaging	1.00
R0049:Vmn2r75	UTSW	7	86,148,101 (GRCm38)	nonsense	probably null
R0049:Vmn2r75	UTSW	7	86,148,101 (GRCm38)	nonsense	probably null
R0083:Vmn2r75	UTSW	7	86,165,658 (GRCm38)	missense	probably benign	0.00
R0108:Vmn2r75	UTSW	7	86,165,658 (GRCm38)	missense	probably benign	0.00
R0276:Vmn2r75	UTSW	7	86,148,307 (GRCm38)	missense	probably benign	0.01
R0320:Vmn2r75	UTSW	7	86,165,080 (GRCm38)	missense	probably benign	0.36
R0471:Vmn2r75	UTSW	7	86,165,513 (GRCm38)	missense	probably benign	0.01
R0562:Vmn2r75	UTSW	7	86,148,241 (GRCm38)	nonsense	probably null
R0631:Vmn2r75	UTSW	7	86,163,270 (GRCm38)	missense	probably null	1.00
R0661:Vmn2r75	UTSW	7	86,165,658 (GRCm38)	missense	probably benign	0.00
R0811:Vmn2r75	UTSW	7	86,165,367 (GRCm38)	missense	probably benign	0.38
R0891:Vmn2r75	UTSW	7	86,164,268 (GRCm38)	missense	possibly damaging	0.81
R1340:Vmn2r75	UTSW	7	86,148,590 (GRCm38)	missense	probably damaging	0.98
R1501:Vmn2r75	UTSW	7	86,165,642 (GRCm38)	missense	possibly damaging	0.85
R1760:Vmn2r75	UTSW	7	86,148,811 (GRCm38)	missense	probably damaging	1.00
R1970:Vmn2r75	UTSW	7	86,148,262 (GRCm38)	missense	probably damaging	1.00
R2060:Vmn2r75	UTSW	7	86,165,164 (GRCm38)	missense	probably benign	0.00
R2292:Vmn2r75	UTSW	7	86,148,936 (GRCm38)	missense	probably damaging	1.00
R3688:Vmn2r75	UTSW	7	86,148,421 (GRCm38)	missense	probably damaging	0.99
R3892:Vmn2r75	UTSW	7	86,164,286 (GRCm38)	missense	probably null	1.00
R4532:Vmn2r75	UTSW	7	86,148,141 (GRCm38)	nonsense	probably null
R4583:Vmn2r75	UTSW	7	86,164,082 (GRCm38)	missense	possibly damaging	0.81
R4592:Vmn2r75	UTSW	7	86,166,286 (GRCm38)	missense	probably benign	0.00
R4792:Vmn2r75	UTSW	7	86,163,170 (GRCm38)	missense	possibly damaging	0.46
R4859:Vmn2r75	UTSW	7	86,148,403 (GRCm38)	missense	probably benign	0.35
R4896:Vmn2r75	UTSW	7	86,171,579 (GRCm38)	missense	probably benign	0.01
R4943:Vmn2r75	UTSW	7	86,165,497 (GRCm38)	missense	probably damaging	1.00
R4992:Vmn2r75	UTSW	7	86,166,167 (GRCm38)	critical splice donor site	probably null
R5048:Vmn2r75	UTSW	7	86,165,527 (GRCm38)	missense	possibly damaging	0.66
R5063:Vmn2r75	UTSW	7	86,164,164 (GRCm38)	missense	probably benign
R5156:Vmn2r75	UTSW	7	86,164,228 (GRCm38)	missense	possibly damaging	0.51
R5243:Vmn2r75	UTSW	7	86,164,239 (GRCm38)	missense	probably damaging	1.00
R5277:Vmn2r75	UTSW	7	86,166,292 (GRCm38)	missense	probably benign
R5574:Vmn2r75	UTSW	7	86,166,302 (GRCm38)	missense	probably benign	0.22
R5622:Vmn2r75	UTSW	7	86,148,494 (GRCm38)	missense	probably benign	0.15
R5680:Vmn2r75	UTSW	7	86,171,571 (GRCm38)	missense	probably benign	0.10
R5884:Vmn2r75	UTSW	7	86,165,370 (GRCm38)	missense	probably benign
R6021:Vmn2r75	UTSW	7	86,171,612 (GRCm38)	missense	probably benign	0.01
R6217:Vmn2r75	UTSW	7	86,166,167 (GRCm38)	critical splice donor site	probably benign
R6242:Vmn2r75	UTSW	7	86,165,384 (GRCm38)	missense	probably damaging	1.00
R6299:Vmn2r75	UTSW	7	86,165,274 (GRCm38)	missense	probably benign	0.12
R6441:Vmn2r75	UTSW	7	86,171,576 (GRCm38)	missense	probably damaging	0.99
R6495:Vmn2r75	UTSW	7	86,164,079 (GRCm38)	missense	probably benign	0.00
R6553:Vmn2r75	UTSW	7	86,164,245 (GRCm38)	missense	probably benign	0.28
R6670:Vmn2r75	UTSW	7	86,148,436 (GRCm38)	missense	probably damaging	1.00
R7078:Vmn2r75	UTSW	7	86,166,360 (GRCm38)	missense	probably damaging	1.00
R7164:Vmn2r75	UTSW	7	86,165,384 (GRCm38)	missense	probably damaging	1.00
R8411:Vmn2r75	UTSW	7	86,148,514 (GRCm38)	missense	probably damaging	1.00
R8507:Vmn2r75	UTSW	7	86,148,477 (GRCm38)	nonsense	probably null
R8559:Vmn2r75	UTSW	7	86,166,272 (GRCm38)	missense	possibly damaging	0.65
R8677:Vmn2r75	UTSW	7	86,165,202 (GRCm38)	missense	possibly damaging	0.86
R8708:Vmn2r75	UTSW	7	86,163,268 (GRCm38)	missense	probably damaging	0.99
R8778:Vmn2r75	UTSW	7	86,164,289 (GRCm38)	missense	probably benign	0.40
R8968:Vmn2r75	UTSW	7	86,171,557 (GRCm38)	nonsense	probably null
R9145:Vmn2r75	UTSW	7	86,164,239 (GRCm38)	missense	probably damaging	1.00
R9316:Vmn2r75	UTSW	7	86,148,105 (GRCm38)	missense	possibly damaging	0.63
R9363:Vmn2r75	UTSW	7	86,166,215 (GRCm38)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- CTTGTTGCAGAAGCATCTCATGCAC -3'
(R):5'- TCCAAACTGAGAAGTTCATGGCCC -3'

Sequencing Primer
(F):5'- AGCATCTCATGCACTGAGTGG -3'
(R):5'- CATGGCCCTTAAAGAGTTTCG -3'

Posted On

2013-10-16