Mutagenetix > Incidental Mutations

Incidental Mutation 'PIT4280001:Vmn2r63'

554413

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r63

Ensembl Gene

ENSMUSG00000090751

Gene Name

vomeronasal 2, receptor 63

Synonyms

EG435975

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.083) question?

Stock #

PIT4280001 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

42903251-42933789 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 42903985 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 616 (T616A)

Ref Sequence

ENSEMBL: ENSMUSP00000129089 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000163803]

Predicted Effect

probably damaging
Transcript: ENSMUST00000163803
AA Change: T616A

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

SMART Domains

Protein: ENSMUSP00000129089
Gene: ENSMUSG00000090751
AA Change: T616A

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	77	471	3.5e-43	PFAM
Pfam:NCD3G	514	567	5.1e-23	PFAM
Pfam:7tm_3	600	835	3.5e-51	PFAM

Coding Region Coverage

1x: 93.1%
3x: 90.9%
10x: 85.5%
20x: 73.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020L24Rik	A	G	11: 83,440,834	D161G	probably damaging	Het
2810474O19Rik	T	G	6: 149,325,525	I23S	probably benign	Het
Acer2	C	T	4: 86,887,083	L95F	probably damaging	Het
Adam15	C	T	3: 89,343,978		probably null	Het
Bmi1	T	A	2: 18,683,009	Y98*	probably null	Het
Cdon	T	C	9: 35,486,935	C983R	probably damaging	Het
Col12a1	T	C	9: 79,678,105	R1297G	probably damaging	Het
Cpd	A	T	11: 76,791,024	M1132K	probably benign	Het
Dnah17	T	A	11: 118,098,582	R1267W	possibly damaging	Het
Dnah9	G	A	11: 66,005,013	A2512V	probably benign	Het
Eri3	G	A	4: 117,582,634	G175D	probably damaging	Het
Fbxo9	C	A	9: 78,087,511	W244L	probably damaging	Het
Fgfr3	A	T	5: 33,732,232	H343L	probably benign	Het
Fmnl2	G	A	2: 53,118,196	A803T	unknown	Het
Fmnl3	A	G	15: 99,321,253		probably null	Het
Fth1	C	A	19: 9,984,609	A104E	probably damaging	Het
Gcm1	T	C	9: 78,059,633	Y45H	probably damaging	Het
Gm5157	C	G	7: 21,185,082	G179R	probably damaging	Het
Gpr179	A	G	11: 97,344,115	I463T	probably damaging	Het
Gpr35	T	C	1: 92,982,634	Y23H	probably damaging	Het
Inpp4b	C	T	8: 82,034,417	H647Y	probably benign	Het
Kif6	A	T	17: 49,755,120	K436M	probably benign	Het
Lacc1	T	A	14: 77,035,077	Q93L	probably damaging	Het
Lamc1	T	C	1: 153,243,471	R801G	probably damaging	Het
Lrp2bp	T	G	8: 46,023,011	V263G	probably damaging	Het
Maats1	C	T	16: 38,332,773	V160I	probably benign	Het
Magi3	T	A	3: 104,054,352	K453N	probably damaging	Het
Mfsd6	T	A	1: 52,660,880	Y703F	probably benign	Het
Mms22l	A	G	4: 24,581,149	T820A	probably benign	Het
Ndufa12	T	C	10: 94,199,132		probably null	Het
Nlrp12	A	T	7: 3,241,433	C150S	possibly damaging	Het
Noc4l	G	A	5: 110,651,439	T159I	probably benign	Het
Olfml2b	T	A	1: 170,647,736	C77S	probably damaging	Het
Olfr1259	A	T	2: 89,943,743	I124N	probably damaging	Het
Olfr460	C	A	6: 40,571,716	T110K	probably damaging	Het
Pdzd2	A	G	15: 12,399,288	V784A	probably damaging	Het
Pip5kl1	A	T	2: 32,583,458	Y369F	probably benign	Het
Pkdrej	A	T	15: 85,819,935	I600N	probably benign	Het
Psg19	T	C	7: 18,796,906	I108V	probably damaging	Het
Pxdn	G	A	12: 29,995,328	V539M	probably damaging	Het
Rsbn1l	T	A	5: 20,919,655	H383L	probably damaging	Het
Scamp2	A	T	9: 57,580,793	N118I	probably damaging	Het
Scn2a	T	C	2: 65,715,730	V879A	probably damaging	Het
Scn8a	G	A	15: 100,957,489	E172K	probably damaging	Het
Slc16a6	C	T	11: 109,458,593	C214Y	possibly damaging	Het
Stag1	A	G	9: 100,942,716	T922A	possibly damaging	Het
Svs1	A	T	6: 48,987,120	M21L	probably benign	Het
Tarbp1	T	C	8: 126,430,847	H1307R	probably damaging	Het
Tut1	T	G	19: 8,959,262	V150G	probably benign	Het
Ubr2	G	A	17: 46,944,863	R1371W	probably damaging	Het
Vmn2r124	A	G	17: 18,063,225	N394D	probably benign	Het
Zp3	G	A	5: 135,984,464	V217M	possibly damaging	Het

Other mutations in Vmn2r63

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01399:Vmn2r63	APN	7	42904119	missense	probably damaging	0.99
IGL01765:Vmn2r63	APN	7	42903364	missense	probably benign
IGL02203:Vmn2r63	APN	7	42904008	missense	probably benign	0.01
IGL02825:Vmn2r63	APN	7	42926850	critical splice donor site	probably null
IGL03155:Vmn2r63	APN	7	42903454	missense	probably damaging	1.00
IGL03260:Vmn2r63	APN	7	42929192	missense	probably damaging	1.00
IGL03411:Vmn2r63	APN	7	42927944	missense	probably benign	0.42
R0066:Vmn2r63	UTSW	7	42927090	splice site	probably benign
R0328:Vmn2r63	UTSW	7	42903275	missense	probably benign	0.09
R0344:Vmn2r63	UTSW	7	42903618	missense	probably damaging	0.98
R0554:Vmn2r63	UTSW	7	42933705	nonsense	probably null
R0555:Vmn2r63	UTSW	7	42928528	nonsense	probably null
R0685:Vmn2r63	UTSW	7	42928010	missense	probably benign	0.13
R0751:Vmn2r63	UTSW	7	42928035	missense	probably damaging	1.00
R1349:Vmn2r63	UTSW	7	42929218	missense	possibly damaging	0.95
R1372:Vmn2r63	UTSW	7	42929218	missense	possibly damaging	0.95
R1416:Vmn2r63	UTSW	7	42927915	missense	probably benign	0.00
R1502:Vmn2r63	UTSW	7	42928591	missense	possibly damaging	0.62
R1563:Vmn2r63	UTSW	7	42904126	missense	probably benign	0.00
R1652:Vmn2r63	UTSW	7	42928211	missense	probably benign	0.32
R1693:Vmn2r63	UTSW	7	42928319	missense	probably benign
R1698:Vmn2r63	UTSW	7	42933614	missense	probably benign
R1753:Vmn2r63	UTSW	7	42928245	nonsense	probably null
R2136:Vmn2r63	UTSW	7	42926873	missense	probably damaging	0.99
R2175:Vmn2r63	UTSW	7	42933580	critical splice donor site	probably null
R2261:Vmn2r63	UTSW	7	42928607	missense	probably benign	0.02
R2262:Vmn2r63	UTSW	7	42928607	missense	probably benign	0.02
R2263:Vmn2r63	UTSW	7	42928607	missense	probably benign	0.02
R3413:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R3426:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R3427:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R3802:Vmn2r63	UTSW	7	42903405	missense	probably damaging	0.99
R4319:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R4321:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R4323:Vmn2r63	UTSW	7	42926982	missense	probably benign	0.04
R4346:Vmn2r63	UTSW	7	42928113	missense	possibly damaging	0.67
R4568:Vmn2r63	UTSW	7	42933826	unclassified	probably null
R4649:Vmn2r63	UTSW	7	42903690	missense	possibly damaging	0.79
R4653:Vmn2r63	UTSW	7	42903690	missense	possibly damaging	0.79
R4679:Vmn2r63	UTSW	7	42928120	missense	probably benign	0.00
R4734:Vmn2r63	UTSW	7	42928120	missense	probably benign	0.00
R4741:Vmn2r63	UTSW	7	42928120	missense	probably benign	0.00
R4748:Vmn2r63	UTSW	7	42928120	missense	probably benign	0.00
R4806:Vmn2r63	UTSW	7	42926890	missense	probably benign	0.34
R4933:Vmn2r63	UTSW	7	42903978	missense	probably damaging	1.00
R5198:Vmn2r63	UTSW	7	42903745	missense	probably benign	0.01
R5399:Vmn2r63	UTSW	7	42928277	missense	probably benign
R5400:Vmn2r63	UTSW	7	42928211	missense	probably benign	0.32
R6158:Vmn2r63	UTSW	7	42933680	missense	probably damaging	1.00
R6185:Vmn2r63	UTSW	7	42929011	missense	probably damaging	0.98
R6267:Vmn2r63	UTSW	7	42928635	intron	probably null
R6362:Vmn2r63	UTSW	7	42903297	missense	probably benign
R6706:Vmn2r63	UTSW	7	42928577	missense	probably damaging	1.00
R6764:Vmn2r63	UTSW	7	42903271	missense	probably damaging	0.97
R7104:Vmn2r63	UTSW	7	42928535	missense	possibly damaging	0.67
R7503:Vmn2r63	UTSW	7	42933590	missense	probably benign	0.02
R7506:Vmn2r63	UTSW	7	42926967	missense	probably damaging	1.00
R7525:Vmn2r63	UTSW	7	42926982	missense	possibly damaging	0.52
R7658:Vmn2r63	UTSW	7	42925269	missense	probably damaging	1.00
R7663:Vmn2r63	UTSW	7	42927042	missense	probably benign	0.00
R7702:Vmn2r63	UTSW	7	42928129	missense	possibly damaging	0.46
Z1088:Vmn2r63	UTSW	7	42928559	missense	probably benign	0.09

Predicted Primers

PCR Primer
(F):5'- ACCATTCTAGCTGGAGAGGTG -3'
(R):5'- GTGTGCAGTGTCCAGAAAGTC -3'

Sequencing Primer
(F):5'- GTGACCTTGAATGCAGTAACC -3'
(R):5'- TGCAGTGTCCAGAAAGTCACTATG -3'

Posted On

2019-06-07