Mutagenetix > Incidental Mutation

Incidental Mutation 'R9457:Vmn2r89'

714679

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r89

Ensembl Gene

ENSMUSG00000070448

Gene Name

vomeronasal 2, receptor 89

Synonyms

V2r10, V2r11

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.208) question?

Stock #

R9457 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

51451962-51461293 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 51456012 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Valine at position 273 (E273V)

Ref Sequence

ENSEMBL: ENSMUSP00000124065 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000159611] [ENSMUST00000159734] [ENSMUST00000161670] [ENSMUST00000162998]

AlphaFold

O35199

Predicted Effect

probably damaging
Transcript: ENSMUST00000159611
AA Change: E273V

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000124065
Gene: ENSMUSG00000070448
AA Change: E273V

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC
Pfam:ANF_receptor	76	449	4.8e-30	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000159734
AA Change: E273V

PolyPhen 2 Score 0.965 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000124256
Gene: ENSMUSG00000070448
AA Change: E273V

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC
Pfam:ANF_receptor	76	420	1.1e-29	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000161670

SMART Domains

Protein: ENSMUSP00000124261
Gene: ENSMUSG00000070448

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000162998

SMART Domains

Protein: ENSMUSP00000125409
Gene: ENSMUSG00000068399

Domain	Start	End	E-Value	Type
Pfam:Takusan	35	115	2.2e-25	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110002H16Rik	A	G	18: 12,179,246	H181R	probably benign	Het
4930404N11Rik	C	A	10: 81,365,777	V4L	probably benign	Het
4930430A15Rik	A	T	2: 111,170,286	M196K	unknown	Het
4932415D10Rik	A	G	10: 82,286,739	V3479A	probably benign	Het
A930009A15Rik	T	C	10: 115,578,331	L54P	unknown	Het
Ablim3	A	G	18: 61,845,849	S204P	probably benign	Het
Acadl	A	G	1: 66,853,241	V141A	probably benign	Het
Ace3	A	G	11: 105,994,861	D31G	probably benign	Het
Adam11	T	G	11: 102,769,898	V85G	probably benign	Het
Adarb1	A	T	10: 77,322,148	M155K	possibly damaging	Het
Arhgap10	G	A	8: 77,384,786	T376M	probably benign	Het
Bod1l	G	T	5: 41,821,967	T668K	probably damaging	Het
Ccdc87	A	G	19: 4,841,631	E717G	probably damaging	Het
Cdh17	T	A	4: 11,771,329	I37N	probably damaging	Het
Cfap99	T	G	5: 34,301,397	F45L	probably benign	Het
Chsy1	C	A	7: 66,172,400	H794Q	probably benign	Het
Clec4a3	G	A	6: 122,954,086	V45I	probably benign	Het
Clic3	G	A	2: 25,457,718	V32I	probably benign	Het
Clip2	A	T	5: 134,502,730	D740E	probably benign	Het
Col5a2	C	T	1: 45,386,844	V1062I	probably benign	Het
Col5a2	A	G	1: 45,392,813		probably null	Het
Cyp2j11	C	T	4: 96,307,359	V367I	probably damaging	Het
Ddr1	C	T	17: 35,682,758	A821T	possibly damaging	Het
Dna2	G	A	10: 62,950,793	E107K	probably benign	Het
Eif3d	A	G	15: 77,959,694	V484A	probably benign	Het
Fgfr4	A	G	13: 55,161,127	T354A	probably benign	Het
Fkbp6	T	C	5: 135,349,632	D54G	probably benign	Het
Gm4787	T	A	12: 81,379,246	E46V	probably damaging	Het
Gm47995	A	G	1: 151,198,475	T10A	possibly damaging	Het
Gm498	T	C	7: 143,883,976	V137A	possibly damaging	Het
Gnb1l	T	A	16: 18,540,995	I50N	probably damaging	Het
Gphb5	A	T	12: 75,415,749	V22D	probably damaging	Het
Gstt4	C	T	10: 75,815,125	C221Y	probably benign	Het
Hmces	T	C	6: 87,933,274	V222A	possibly damaging	Het
Kat14	T	A	2: 144,373,782	D62E	probably benign	Het
Kcnmb2	T	A	3: 32,181,869	V89E	probably benign	Het
Kif23	T	A	9: 61,944,225	N63I	probably benign	Het
Lamc2	T	C	1: 153,139,854	M578V	probably benign	Het
Ltbp2	A	T	12: 84,789,153	C1335S	probably benign	Het
Lyst	A	G	13: 13,687,745	E2622G	possibly damaging	Het
Mctp1	A	T	13: 76,384,674	H47L	probably benign	Het
Micalcl	A	G	7: 112,411,458	K618R	probably damaging	Het
Mllt6	T	C	11: 97,665,760	I92T	probably benign	Het
Morc2a	A	G	11: 3,676,184	I223V	probably benign	Het
Msh3	A	T	13: 92,345,086	I306N	probably benign	Het
Myo3b	T	A	2: 70,095,209	S35T	probably benign	Het
Nfkbiz	A	T	16: 55,813,984	V700E	probably damaging	Het
Oit3	T	A	10: 59,441,683	M1L	unknown	Het
Olfr1048	A	T	2: 86,236,472	I114K	probably damaging	Het
Olfr1231	A	T	2: 89,302,731	I287N	probably damaging	Het
Olfr606	T	A	7: 103,451,411	F25I	probably benign	Het
Peg3	T	G	7: 6,707,999	D1408A	probably damaging	Het
Plaa	A	C	4: 94,586,883	S201R	possibly damaging	Het
Psmd5	A	G	2: 34,854,326	S395P	probably benign	Het
Ralgapa2	T	C	2: 146,334,554	I1701V	probably damaging	Het
Rnf32	G	A	5: 29,206,186	A157T	probably damaging	Het
Rrad	T	A	8: 104,629,727		probably null	Het
Samm50	T	A	15: 84,207,841	L339Q	probably damaging	Het
Scin	T	C	12: 40,104,958	E212G	possibly damaging	Het
Scrib	T	C	15: 76,067,299	D146G	probably damaging	Het
Slc19a1	G	A	10: 77,049,771	D502N	probably benign	Het
Slc4a4	T	C	5: 89,214,573	S839P	probably damaging	Het
Slc4a8	A	G	15: 100,806,260	D764G	probably damaging	Het
Slc6a19	G	A	13: 73,681,765	A590V	probably damaging	Het
Slfn8	G	T	11: 83,017,706	H4N	probably benign	Het
Smad9	T	A	3: 54,789,335	F274I	possibly damaging	Het
Snx4	A	G	16: 33,286,010	E271G	probably benign	Het
Thap4	G	A	1: 93,750,306	R253*	probably null	Het
Tmem65	T	A	15: 58,790,179	I144F		Het
Tnrc6a	G	A	7: 123,179,735	R1223Q	probably benign	Het
Traf7	CA	CAA	17: 24,527,763		probably benign	Het
Trpm2	T	C	10: 77,911,392	Y1424C	possibly damaging	Het
Trrap	T	A	5: 144,826,668	Y2457N	probably damaging	Het
Vmn1r7	A	G	6: 57,024,523	S251P	probably damaging	Het
Vps52	A	G	17: 33,962,182	D466G	probably damaging	Het
Xirp2	T	C	2: 67,515,632	V2739A	probably benign	Het
Zc3h4	C	T	7: 16,434,750	S1003F	unknown	Het
Zyg11a	A	T	4: 108,217,905	H6Q	probably damaging	Het

Other mutations in Vmn2r89

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00433:Vmn2r89	APN	14	51,454,965 (GRCm38)	missense	probably damaging	1.00
IGL00990:Vmn2r89	APN	14	51,457,493 (GRCm38)	missense	probably benign
IGL00990:Vmn2r89	APN	14	51,455,971 (GRCm38)	missense	probably benign	0.14
IGL01991:Vmn2r89	APN	14	51,452,219 (GRCm38)	missense	probably benign	0.00
IGL03073:Vmn2r89	APN	14	51,456,071 (GRCm38)	missense	possibly damaging	0.95
IGL03085:Vmn2r89	APN	14	51,452,158 (GRCm38)	missense	probably damaging	0.99
IGL03278:Vmn2r89	APN	14	51,455,100 (GRCm38)	missense	probably damaging	0.99
R0115:Vmn2r89	UTSW	14	51,456,120 (GRCm38)	missense	probably damaging	1.00
R0127:Vmn2r89	UTSW	14	51,455,703 (GRCm38)	missense	probably damaging	0.98
R0391:Vmn2r89	UTSW	14	51,455,978 (GRCm38)	missense	probably damaging	0.99
R0481:Vmn2r89	UTSW	14	51,456,120 (GRCm38)	missense	probably damaging	1.00
R0538:Vmn2r89	UTSW	14	51,457,591 (GRCm38)	splice site	probably null
R1210:Vmn2r89	UTSW	14	51,454,970 (GRCm38)	missense	probably benign	0.01
R1332:Vmn2r89	UTSW	14	51,455,102 (GRCm38)	missense	probably benign	0.00
R1660:Vmn2r89	UTSW	14	51,456,236 (GRCm38)	missense	possibly damaging	0.48
R1959:Vmn2r89	UTSW	14	51,457,440 (GRCm38)	missense	probably benign	0.22
R2876:Vmn2r89	UTSW	14	51,455,084 (GRCm38)	missense	possibly damaging	0.47
R3410:Vmn2r89	UTSW	14	51,456,171 (GRCm38)	missense	probably damaging	0.98
R4026:Vmn2r89	UTSW	14	51,452,043 (GRCm38)	start codon destroyed	probably null	1.00
R4398:Vmn2r89	UTSW	14	51,452,094 (GRCm38)	missense	probably damaging	1.00
R4700:Vmn2r89	UTSW	14	51,457,485 (GRCm38)	missense	probably damaging	1.00
R4714:Vmn2r89	UTSW	14	51,452,231 (GRCm38)	missense	probably damaging	0.97
R5162:Vmn2r89	UTSW	14	51,456,163 (GRCm38)	missense	possibly damaging	0.88
R5294:Vmn2r89	UTSW	14	51,455,113 (GRCm38)	missense	probably benign	0.00
R5811:Vmn2r89	UTSW	14	51,456,108 (GRCm38)	missense	probably benign	0.12
R6087:Vmn2r89	UTSW	14	51,457,576 (GRCm38)	splice site	probably null
R6229:Vmn2r89	UTSW	14	51,455,721 (GRCm38)	missense	probably benign	0.05
R6246:Vmn2r89	UTSW	14	51,456,046 (GRCm38)	missense	probably damaging	1.00
R6572:Vmn2r89	UTSW	14	51,455,993 (GRCm38)	missense	probably damaging	1.00
R7351:Vmn2r89	UTSW	14	51,456,282 (GRCm38)	missense	probably benign	0.30
R7683:Vmn2r89	UTSW	14	51,455,194 (GRCm38)	missense	probably benign
R7974:Vmn2r89	UTSW	14	51,456,002 (GRCm38)	missense	probably damaging	1.00
R8047:Vmn2r89	UTSW	14	51,455,092 (GRCm38)	missense	probably benign	0.05
R8093:Vmn2r89	UTSW	14	51,456,242 (GRCm38)	missense	probably benign	0.00
R8348:Vmn2r89	UTSW	14	51,455,091 (GRCm38)	missense	possibly damaging	0.90
R8723:Vmn2r89	UTSW	14	51,456,453 (GRCm38)	missense	probably benign
R8737:Vmn2r89	UTSW	14	51,456,265 (GRCm38)	missense	probably damaging	1.00
R8859:Vmn2r89	UTSW	14	51,455,713 (GRCm38)	missense	probably benign
R9183:Vmn2r89	UTSW	14	51,455,044 (GRCm38)	missense	probably benign	0.01
R9197:Vmn2r89	UTSW	14	51,456,139 (GRCm38)	missense	possibly damaging	0.70
R9377:Vmn2r89	UTSW	14	51,455,144 (GRCm38)	missense	probably benign	0.02
R9395:Vmn2r89	UTSW	14	51,456,326 (GRCm38)	missense	probably damaging	1.00
R9452:Vmn2r89	UTSW	14	51,455,831 (GRCm38)	missense	probably damaging	0.99
R9678:Vmn2r89	UTSW	14	51,456,054 (GRCm38)	missense	probably benign	0.09
X0019:Vmn2r89	UTSW	14	51,456,415 (GRCm38)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- TGACCAGGGTATTCAGTTTCTCTC -3'
(R):5'- TGTGCAGTGCTGTCCATTCC -3'

Sequencing Primer
(F):5'- CTCTCAGATTTAAGAGAAGAAAGCC -3'
(R):5'- GCAGTGCTGTCCATTCCAATGTG -3'

Posted On

2022-06-15