Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL03396:Vmn2r23'

421246

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn2r23

Ensembl Gene

ENSMUSG00000091620

Gene Name

vomeronasal 2, receptor 23

Synonyms

EG435916

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

IGL03396

Quality Score

Status

Chromosome

Chromosomal Location

123702821-123742291 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 123729626 bp

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 472 (S472P)

Ref Sequence

ENSEMBL: ENSMUSP00000126682 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000172391]

Predicted Effect

probably damaging
Transcript: ENSMUST00000172391
AA Change: S472P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000126682
Gene: ENSMUSG00000091620
AA Change: S472P

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:ANF_receptor	79	461	1.7e-31	PFAM
Pfam:NCD3G	513	566	1.2e-23	PFAM
Pfam:7tm_3	596	834	1.5e-55	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acadvl	G	A	11: 70,011,413	R457*	probably null	Het
Arl5b	C	A	2: 15,075,104	T153K	probably damaging	Het
Arsb	A	T	13: 93,939,317	Y436F	probably benign	Het
Azgp1	C	T	5: 137,985,183	P40L	possibly damaging	Het
B020004C17Rik	A	G	14: 57,016,536	T39A	possibly damaging	Het
Cacna2d3	G	A	14: 29,720,877	Q67*	probably null	Het
Cdcp2	C	A	4: 107,107,172	Y406*	probably null	Het
Cep89	T	A	7: 35,429,178	D585E	probably benign	Het
Cfap65	A	G	1: 74,904,642	F1570S	probably damaging	Het
Cnfn	A	G	7: 25,368,358		probably benign	Het
Fgd6	G	A	10: 94,044,456	V391I	probably benign	Het
Fra10ac1	C	T	19: 38,201,546		probably null	Het
Gjc1	T	C	11: 102,800,527	K217E	probably benign	Het
Il20rb	T	C	9: 100,459,198	E285G	probably damaging	Het
Ints2	T	C	11: 86,213,062	T1086A	probably damaging	Het
Itih4	A	T	14: 30,887,949	I79F	probably damaging	Het
Jmjd6	A	T	11: 116,841,251	L208H	probably damaging	Het
Lilr4b	A	G	10: 51,481,157	I30V	possibly damaging	Het
Limch1	A	G	5: 66,953,673	N81S	probably damaging	Het
Mettl21e	A	T	1: 44,206,599	N162K	possibly damaging	Het
Ninl	A	G	2: 150,966,212	S299P	possibly damaging	Het
Obscn	A	G	11: 59,073,578	L3046P	probably benign	Het
Olfr1450	T	A	19: 12,953,820	V77E	probably damaging	Het
Olfr342	C	A	2: 36,527,680	S89R	probably benign	Het
Olfr780	A	G	10: 129,322,047	I141M	probably benign	Het
Pnpla8	G	A	12: 44,283,526	R287H	probably benign	Het
Pot1a	A	C	6: 25,745,914	I596R	possibly damaging	Het
Prkaa1	A	G	15: 5,176,650	D329G	probably damaging	Het
Ptprr	T	G	10: 116,188,330	V182G	probably damaging	Het
Rrp1b	T	A	17: 32,057,263		probably benign	Het
Sec24a	A	G	11: 51,708,967	V837A	probably benign	Het
Slc17a6	A	G	7: 51,669,092	Y494C	probably damaging	Het
Slc38a10	A	T	11: 120,128,475	I360N	probably damaging	Het
Snrpb2	T	C	2: 143,071,457	F194L	possibly damaging	Het
Tcam1	A	G	11: 106,285,386	I313V	probably benign	Het
Trpv1	A	G	11: 73,253,056	N238S	probably benign	Het
Usp20	T	C	2: 31,011,717	V498A	probably benign	Het
Vmn2r98	A	T	17: 19,069,845	T548S	possibly damaging	Het
Zfp429	A	T	13: 67,396,040		probably benign	Het

Other mutations in Vmn2r23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00324:Vmn2r23	APN	6	123729725	missense	possibly damaging	0.89
IGL01012:Vmn2r23	APN	6	123729596	missense	probably benign
IGL01073:Vmn2r23	APN	6	123712800	missense	possibly damaging	0.82
IGL01547:Vmn2r23	APN	6	123704424	missense	possibly damaging	0.88
IGL01571:Vmn2r23	APN	6	123704407	missense	probably damaging	1.00
IGL01950:Vmn2r23	APN	6	123741886	missense	possibly damaging	0.80
IGL02028:Vmn2r23	APN	6	123741860	missense	probably damaging	1.00
IGL02248:Vmn2r23	APN	6	123741744	missense	probably damaging	0.96
IGL02318:Vmn2r23	APN	6	123741836	missense	probably benign	0.10
IGL02649:Vmn2r23	APN	6	123704478	missense	probably benign
IGL02831:Vmn2r23	APN	6	123704385	missense	probably benign	0.22
IGL02832:Vmn2r23	APN	6	123704396	missense	probably benign	0.00
IGL02865:Vmn2r23	APN	6	123741619	missense	probably damaging	1.00
IGL02964:Vmn2r23	APN	6	123741782	missense	possibly damaging	0.93
IGL03347:Vmn2r23	APN	6	123704374	missense	probably benign	0.01
PIT4472001:Vmn2r23	UTSW	6	123712977	missense	possibly damaging	0.62
R0597:Vmn2r23	UTSW	6	123729721	missense	probably benign	0.08
R0677:Vmn2r23	UTSW	6	123713451	missense	probably benign	0.00
R0904:Vmn2r23	UTSW	6	123742135	missense	probably damaging	1.00
R1330:Vmn2r23	UTSW	6	123742004	missense	probably damaging	1.00
R1424:Vmn2r23	UTSW	6	123713270	nonsense	probably null
R1629:Vmn2r23	UTSW	6	123713427	missense	probably benign	0.05
R1842:Vmn2r23	UTSW	6	123729690	missense	possibly damaging	0.77
R1867:Vmn2r23	UTSW	6	123702915	missense	probably damaging	1.00
R1919:Vmn2r23	UTSW	6	123713010	missense	possibly damaging	0.94
R2087:Vmn2r23	UTSW	6	123741499	missense	probably benign	0.00
R2338:Vmn2r23	UTSW	6	123704425	missense	possibly damaging	0.88
R2568:Vmn2r23	UTSW	6	123742188	nonsense	probably null
R2867:Vmn2r23	UTSW	6	123713164	missense	possibly damaging	0.94
R2867:Vmn2r23	UTSW	6	123713164	missense	possibly damaging	0.94
R3500:Vmn2r23	UTSW	6	123713170	missense	possibly damaging	0.81
R3789:Vmn2r23	UTSW	6	123741389	missense	probably damaging	1.00
R4164:Vmn2r23	UTSW	6	123729738	missense	probably benign
R4506:Vmn2r23	UTSW	6	123702925	missense	probably damaging	1.00
R4652:Vmn2r23	UTSW	6	123741730	missense	probably damaging	1.00
R4697:Vmn2r23	UTSW	6	123741826	missense	probably damaging	1.00
R4840:Vmn2r23	UTSW	6	123713074	missense	probably damaging	1.00
R4983:Vmn2r23	UTSW	6	123733349	missense	probably damaging	1.00
R5276:Vmn2r23	UTSW	6	123712977	missense	possibly damaging	0.62
R5392:Vmn2r23	UTSW	6	123704364	missense	probably benign	0.36
R5528:Vmn2r23	UTSW	6	123713002	missense	probably damaging	1.00
R5529:Vmn2r23	UTSW	6	123713451	missense	probably benign	0.00
R5664:Vmn2r23	UTSW	6	123713074	missense	probably damaging	1.00
R5749:Vmn2r23	UTSW	6	123733273	missense	probably benign
R5761:Vmn2r23	UTSW	6	123712759	missense	probably benign	0.39
R5762:Vmn2r23	UTSW	6	123733393	missense	probably damaging	1.00
R5868:Vmn2r23	UTSW	6	123712942	missense	probably benign	0.12
R5935:Vmn2r23	UTSW	6	123741895	missense	possibly damaging	0.94
R6242:Vmn2r23	UTSW	6	123704400	missense	possibly damaging	0.82
R6416:Vmn2r23	UTSW	6	123712902	missense	probably damaging	1.00
R6524:Vmn2r23	UTSW	6	123713425	missense	probably damaging	1.00
R6576:Vmn2r23	UTSW	6	123733273	missense	probably benign
R6925:Vmn2r23	UTSW	6	123704553	missense	probably damaging	1.00
R7148:Vmn2r23	UTSW	6	123713022	missense	probably benign
R7215:Vmn2r23	UTSW	6	123704364	missense	probably benign	0.36
R7252:Vmn2r23	UTSW	6	123741581	missense	probably damaging	0.97
R7403:Vmn2r23	UTSW	6	123704579	missense	probably benign	0.01
R8015:Vmn2r23	UTSW	6	123704541	missense	probably benign	0.00
R8143:Vmn2r23	UTSW	6	123741353	missense	probably damaging	0.99
R8474:Vmn2r23	UTSW	6	123704640	missense	probably benign	0.36
R8520:Vmn2r23	UTSW	6	123741656	missense	probably damaging	0.99
RF018:Vmn2r23	UTSW	6	123713116	missense	probably benign	0.00
T0975:Vmn2r23	UTSW	6	123713161	missense	probably benign	0.00
Z1088:Vmn2r23	UTSW	6	123742108	missense	probably damaging	0.98
Z1177:Vmn2r23	UTSW	6	123729725	frame shift	probably null

Posted On

2016-08-02