Mutagenetix > Incidental Mutation

Incidental Mutation 'R8191:Vmn2r125'

635144

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r125

Ensembl Gene

ENSMUSG00000096042

Gene Name

vomeronasal 2, receptor 125

Synonyms

Gm20782

MMRRC Submission

067614-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R8191 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

156696567-156708037 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 156703709 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Tryptophan at position 362 (C362W)

Ref Sequence

ENSEMBL: ENSMUSP00000094556 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096794]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000096794
AA Change: C362W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000094556
Gene: ENSMUSG00000096042
AA Change: C362W

Domain	Start	End	E-Value	Type
Pfam:ANF_receptor	9	355	7e-32	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700037C18Rik	G	A	16: 3,724,918 (GRCm39)	R49W	probably damaging	Het
Adamts4	T	C	1: 171,080,292 (GRCm39)	S282P		Het
Aqp4	A	G	18: 15,531,222 (GRCm39)	S180P	probably benign	Het
Armc2	T	G	10: 41,839,747 (GRCm39)	E406A	probably benign	Het
Atp13a3	A	T	16: 30,168,598 (GRCm39)	Y464N	probably damaging	Het
B3gnt3	C	A	8: 72,146,122 (GRCm39)	V136L	probably benign	Het
Cacna1s	C	T	1: 136,035,893 (GRCm39)	H1378Y	probably damaging	Het
Ccnk	A	T	12: 108,159,933 (GRCm39)	E138D	probably benign	Het
Cenpe	A	G	3: 134,957,375 (GRCm39)	K1878E	probably benign	Het
Cep57l1	T	A	10: 41,616,955 (GRCm39)	I111L	probably damaging	Het
Cfap298	G	T	16: 90,727,889 (GRCm39)	N100K	probably damaging	Het
Copg2	T	C	6: 30,790,665 (GRCm39)	I509V	probably benign	Het
Cux2	T	A	5: 122,012,217 (GRCm39)	D406V	probably benign	Het
Cyp2a12	G	T	7: 26,730,529 (GRCm39)	A165S	probably benign	Het
Dnaaf5	T	G	5: 139,167,250 (GRCm39)	S719A	probably benign	Het
Dnah7c	A	G	1: 46,646,618 (GRCm39)	I1220V	possibly damaging	Het
Dnai3	G	T	3: 145,800,066 (GRCm39)	P158H	probably damaging	Het
Dnajb8	C	T	6: 88,199,940 (GRCm39)	R159C	possibly damaging	Het
Dusp10	T	A	1: 183,769,749 (GRCm39)	D238E	possibly damaging	Het
Dync1li1	C	A	9: 114,538,253 (GRCm39)	D203E	probably benign	Het
Ecpas	A	T	4: 58,872,587 (GRCm39)		probably null	Het
Eif5b	T	C	1: 38,075,283 (GRCm39)	S587P	probably damaging	Het
Ephb2	G	A	4: 136,386,256 (GRCm39)	T832I	probably damaging	Het
Exoc1	T	A	5: 76,707,674 (GRCm39)		probably null	Het
Fam193a	T	A	5: 34,597,917 (GRCm39)	N571K	probably damaging	Het
Fem1a	T	A	17: 56,565,356 (GRCm39)	I483N	probably damaging	Het
Fgf20	C	A	8: 40,761,361 (GRCm39)		probably benign	Het
Fkbp1a	C	T	2: 151,399,356 (GRCm39)	P98S		Het
Gpsm3	A	T	17: 34,809,451 (GRCm39)	D19V	probably benign	Het
Ido2	C	A	8: 25,023,696 (GRCm39)	G381W	probably damaging	Het
Ifi204	T	C	1: 173,579,226 (GRCm39)	T540A	possibly damaging	Het
Isl1	A	T	13: 116,441,954 (GRCm39)	M93K	probably benign	Het
Map3k10	T	A	7: 27,362,671 (GRCm39)	S472C	probably damaging	Het
Mcrs1	A	T	15: 99,141,206 (GRCm39)	V432E	probably damaging	Het
Metap2	A	G	10: 93,701,267 (GRCm39)		probably null	Het
Muc5b	A	G	7: 141,421,421 (GRCm39)	S4304G	probably benign	Het
Myef2l	G	T	3: 10,153,914 (GRCm39)	V228F	probably damaging	Het
Nell1	T	C	7: 50,098,622 (GRCm39)	V308A	unknown	Het
Or10g1b	A	G	14: 52,627,987 (GRCm39)	V81A	probably benign	Het
Or4d5	A	T	9: 40,012,767 (GRCm39)	H6Q	probably benign	Het
Plxna4	C	A	6: 32,493,885 (GRCm39)	V244F	possibly damaging	Het
Pnpla6	T	C	8: 3,592,382 (GRCm39)	S1224P	probably benign	Het
Ripk4	A	G	16: 97,564,726 (GRCm39)		probably benign	Het
Rnpep	T	C	1: 135,200,172 (GRCm39)	E261G	possibly damaging	Het
Robo1	C	A	16: 72,730,142 (GRCm39)	S194R	probably damaging	Het
Rpusd1	C	G	17: 25,947,611 (GRCm39)	Y99*	probably null	Het
Scarf1	T	C	11: 75,413,065 (GRCm39)	M437T	probably benign	Het
Sh3tc2	G	T	18: 62,106,429 (GRCm39)	D153Y	probably damaging	Het
Siglec1	T	C	2: 130,927,599 (GRCm39)	Y69C	probably damaging	Het
Slc25a34	T	C	4: 141,347,895 (GRCm39)	Y262C	probably damaging	Het
Srrm2	T	A	17: 24,039,219 (GRCm39)	N1954K	probably damaging	Het
St6galnac2	T	C	11: 116,572,748 (GRCm39)	Y236C	probably damaging	Het
Stac3	T	A	10: 127,344,068 (GRCm39)	I322N	probably damaging	Het
Tcaf1	T	C	6: 42,652,190 (GRCm39)	Q764R	probably damaging	Het
Tcf20	G	A	15: 82,737,606 (GRCm39)	R1282*	probably null	Het
Tlr2	T	A	3: 83,743,821 (GRCm39)	K754M	probably damaging	Het
Tlr2	T	G	3: 83,743,822 (GRCm39)	K754Q	probably damaging	Het
Tnn	C	T	1: 159,953,088 (GRCm39)	V651M	probably damaging	Het
Ttn	T	C	2: 76,701,083 (GRCm39)	H9622R	unknown	Het
Tubgcp6	C	T	15: 89,004,843 (GRCm39)	G259S	probably damaging	Het
Ubr5	C	A	15: 38,006,751 (GRCm39)	C1174F		Het
Ugt2b35	T	A	5: 87,149,302 (GRCm39)	S184R	probably damaging	Het
Vit	C	T	17: 78,853,828 (GRCm39)	H25Y	probably benign	Het
Vmn1r177	G	A	7: 23,565,736 (GRCm39)	Q47*	probably null	Het
Vmn2r104	A	T	17: 20,250,465 (GRCm39)	V602D	possibly damaging	Het
Vmn2r115	A	G	17: 23,578,530 (GRCm39)	T668A	probably damaging	Het
Vwa7	A	G	17: 35,238,712 (GRCm39)	T267A	probably damaging	Het
Xpa	C	A	4: 46,183,225 (GRCm39)	R188L	possibly damaging	Het
Zfp143	C	T	7: 109,676,364 (GRCm39)	T249I	probably damaging	Het
Zfp607a	A	G	7: 27,578,868 (GRCm39)	E646G	possibly damaging	Het
Zfp729a	A	T	13: 67,769,838 (GRCm39)	S130R	probably benign	Het
Zswim3	C	A	2: 164,662,128 (GRCm39)	Q203K	probably damaging	Het

Other mutations in Vmn2r125

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00990:Vmn2r125	APN	4	156,703,194 (GRCm39)	missense	probably benign
IGL00990:Vmn2r125	APN	4	156,703,333 (GRCm39)	missense	probably benign	0.06
IGL00990:Vmn2r125	APN	4	156,703,332 (GRCm39)	missense	probably benign	0.16
IGL00990:Vmn2r125	APN	4	156,703,521 (GRCm39)	missense	probably benign
IGL00990:Vmn2r125	APN	4	156,703,678 (GRCm39)	missense	probably benign	0.00
IGL00990:Vmn2r125	APN	4	156,703,261 (GRCm39)	missense	probably benign	0.01
IGL00990:Vmn2r125	APN	4	156,703,195 (GRCm39)	missense	probably benign	0.35
IGL01018:Vmn2r125	APN	4	156,703,333 (GRCm39)	missense	probably benign	0.06
IGL01018:Vmn2r125	APN	4	156,703,332 (GRCm39)	missense	probably benign	0.16
IGL01018:Vmn2r125	APN	4	156,703,521 (GRCm39)	missense	probably benign
IGL01018:Vmn2r125	APN	4	156,703,195 (GRCm39)	missense	probably benign	0.35
IGL01018:Vmn2r125	APN	4	156,703,194 (GRCm39)	missense	probably benign
IGL01018:Vmn2r125	APN	4	156,703,140 (GRCm39)	missense	probably damaging	1.00
IGL01018:Vmn2r125	APN	4	156,702,907 (GRCm39)	splice site	probably benign
IGL02644:Vmn2r125	APN	4	156,703,294 (GRCm39)	missense	probably benign	0.01
IGL03144:Vmn2r125	APN	4	156,702,314 (GRCm39)	missense	possibly damaging	0.76
BB013:Vmn2r125	UTSW	4	156,702,988 (GRCm39)	missense	probably damaging	1.00
FR4342:Vmn2r125	UTSW	4	156,703,260 (GRCm39)	missense	probably benign	0.01
R0408:Vmn2r125	UTSW	4	156,703,153 (GRCm39)	missense	probably damaging	0.99
R0785:Vmn2r125	UTSW	4	156,703,396 (GRCm39)	missense	probably benign
R1185:Vmn2r125	UTSW	4	156,703,396 (GRCm39)	missense	probably benign
R1185:Vmn2r125	UTSW	4	156,703,396 (GRCm39)	missense	probably benign
R1530:Vmn2r125	UTSW	4	156,703,447 (GRCm39)	missense	probably damaging	1.00
R1698:Vmn2r125	UTSW	4	156,703,333 (GRCm39)	missense	probably benign	0.06
R1780:Vmn2r125	UTSW	4	156,703,668 (GRCm39)	missense	probably damaging	1.00
R1977:Vmn2r125	UTSW	4	156,707,162 (GRCm39)	splice site	probably null
R2917:Vmn2r125	UTSW	4	156,703,564 (GRCm39)	missense	probably benign	0.01
R3428:Vmn2r125	UTSW	4	156,702,436 (GRCm39)	missense	probably benign	0.34
R3712:Vmn2r125	UTSW	4	156,702,419 (GRCm39)	nonsense	probably null
R4274:Vmn2r125	UTSW	4	156,702,382 (GRCm39)	missense	probably benign	0.00
R4575:Vmn2r125	UTSW	4	156,702,272 (GRCm39)	missense	probably null	0.30
R4707:Vmn2r125	UTSW	4	156,702,276 (GRCm39)	missense	probably damaging	1.00
R5229:Vmn2r125	UTSW	4	156,703,333 (GRCm39)	missense	probably benign	0.06
R5504:Vmn2r125	UTSW	4	156,703,456 (GRCm39)	missense	possibly damaging	0.81
R5587:Vmn2r125	UTSW	4	156,702,433 (GRCm39)	missense	probably damaging	1.00
R5987:Vmn2r125	UTSW	4	156,702,292 (GRCm39)	missense	probably damaging	1.00
R6037:Vmn2r125	UTSW	4	156,703,396 (GRCm39)	missense	probably benign
R6183:Vmn2r125	UTSW	4	156,702,364 (GRCm39)	missense	probably damaging	0.97
R6456:Vmn2r125	UTSW	4	156,703,357 (GRCm39)	missense	probably benign	0.41
R7342:Vmn2r125	UTSW	4	156,703,138 (GRCm39)	missense	probably damaging	1.00
R7926:Vmn2r125	UTSW	4	156,702,988 (GRCm39)	missense	probably damaging	1.00
R8113:Vmn2r125	UTSW	4	156,703,642 (GRCm39)	missense	probably damaging	1.00
R8272:Vmn2r125	UTSW	4	156,702,373 (GRCm39)	missense	probably damaging	1.00
R8962:Vmn2r125	UTSW	4	156,703,186 (GRCm39)	missense	possibly damaging	0.50
R9187:Vmn2r125	UTSW	4	156,703,554 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AACACATTGCAATGGACAGC -3'
(R):5'- CTAGTCTAAGTCATCACTTAAGGCTC -3'

Sequencing Primer
(F):5'- TTGCAATGGACAGCACTGC -3'
(R):5'- GGCTCTTATGATAAAAGTCTTGGTTC -3'

Posted On

2020-07-13