Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01955:Vmn1r82'

181433

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn1r82

Ensembl Gene

ENSMUSG00000058132

Gene Name

vomeronasal 1 receptor 82

Synonyms

V1rg12

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

IGL01955

Quality Score

Status

Chromosome

Chromosomal Location

12038732-12039646 bp(+) (GRCm39)

Type of Mutation

splice site (4 bp from exon)

DNA Base Change (assembly)

A to C at 12039650 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000140782 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072801] [ENSMUST00000191002] [ENSMUST00000227672]

AlphaFold

A0A087WRV1

Predicted Effect

probably benign
Transcript: ENSMUST00000072801

SMART Domains

Protein: ENSMUSP00000072580
Gene: ENSMUSG00000058132

Domain	Start	End	E-Value	Type
Pfam:V1R	35	295	1.3e-28	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000191002

SMART Domains

Protein: ENSMUSP00000140782
Gene: ENSMUSG00000058132

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
Pfam:V1R	36	296	8.4e-27	PFAM
Pfam:7tm_1	39	290	2e-5	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000227672

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
4930432E11Rik	G	T	7: 29,273,420 (GRCm39)		noncoding transcript	Het
Abcc1	T	A	16: 14,228,659 (GRCm39)	I302N	probably damaging	Het
Abhd16a	A	G	17: 35,320,316 (GRCm39)	S394G	probably damaging	Het
Adgrv1	T	C	13: 81,330,902 (GRCm39)	Y71C	probably damaging	Het
Apol8	A	G	15: 77,633,899 (GRCm39)	C226R	probably benign	Het
Bbs7	A	G	3: 36,664,471 (GRCm39)	S45P	probably benign	Het
Cacna1b	T	C	2: 24,529,149 (GRCm39)	Y1575C	probably damaging	Het
Cckbr	T	A	7: 105,084,169 (GRCm39)	V301E	probably damaging	Het
Cwc27	A	G	13: 104,944,245 (GRCm39)	Y79H	probably damaging	Het
Dchs1	T	C	7: 105,406,798 (GRCm39)	T2236A	probably benign	Het
Ddx50	T	C	10: 62,482,962 (GRCm39)	R36G	probably benign	Het
Extl3	T	A	14: 65,313,415 (GRCm39)	Y589F	probably benign	Het
Gab2	T	C	7: 96,953,430 (GRCm39)	V601A	probably damaging	Het
Hsd3b1	T	A	3: 98,760,463 (GRCm39)	N176I	probably benign	Het
L3mbtl3	A	T	10: 26,194,336 (GRCm39)	S420R	unknown	Het
Odad2	C	T	18: 7,127,291 (GRCm39)	R974Q	possibly damaging	Het
Or2ak6	T	C	11: 58,592,955 (GRCm39)	S143P	probably damaging	Het
Or52e2	T	A	7: 102,804,061 (GRCm39)	K298*	probably null	Het
Or5g23	A	G	2: 85,439,051 (GRCm39)	F68L	probably benign	Het
Polr2a	T	C	11: 69,632,674 (GRCm39)	D974G	probably damaging	Het
Ptges3l	T	C	11: 101,314,644 (GRCm39)	K13E	possibly damaging	Het
Ptprk	A	G	10: 28,471,861 (GRCm39)		probably benign	Het
Rassf3	T	C	10: 121,253,027 (GRCm39)	Y60C	probably damaging	Het
Rnf157	T	C	11: 116,250,722 (GRCm39)	T160A	probably damaging	Het
Secisbp2l	A	G	2: 125,585,732 (GRCm39)		probably null	Het
Setd2	A	G	9: 110,378,386 (GRCm39)	T734A	probably benign	Het
Skint5	A	G	4: 113,480,933 (GRCm39)		probably null	Het
Slc38a9	A	G	13: 112,831,952 (GRCm39)		probably benign	Het
Snx17	T	G	5: 31,354,426 (GRCm39)		probably benign	Het
Tas2r113	A	T	6: 132,870,817 (GRCm39)	M282L	probably benign	Het
Tbc1d31	A	G	15: 57,805,766 (GRCm39)	N404D	probably benign	Het
Tmem63c	A	T	12: 87,123,982 (GRCm39)	I487F	probably benign	Het
Tpm3	A	G	3: 89,995,742 (GRCm39)	M164V	probably benign	Het
Trafd1	G	T	5: 121,513,217 (GRCm39)	N340K	probably benign	Het
Trpv4	T	A	5: 114,760,743 (GRCm39)	K863*	probably null	Het
Ttn	A	T	2: 76,627,696 (GRCm39)	M13003K	possibly damaging	Het
Tulp1	G	A	17: 28,575,398 (GRCm39)	T103M	probably damaging	Het
Unc5b	T	C	10: 60,614,034 (GRCm39)	T272A	probably benign	Het
Zc3h7b	A	G	15: 81,676,205 (GRCm39)	N704D	probably benign	Het

Other mutations in Vmn1r82

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01509:Vmn1r82	APN	7	12,039,096 (GRCm39)	missense	probably damaging	0.99
IGL02267:Vmn1r82	APN	7	12,039,273 (GRCm39)	missense	probably damaging	1.00
R0336:Vmn1r82	UTSW	7	12,039,248 (GRCm39)	missense	probably benign	0.26
R2373:Vmn1r82	UTSW	7	12,038,982 (GRCm39)	missense	probably damaging	0.99
R2849:Vmn1r82	UTSW	7	12,039,333 (GRCm39)	missense	probably damaging	1.00
R4621:Vmn1r82	UTSW	7	12,039,263 (GRCm39)	missense	possibly damaging	0.71
R5628:Vmn1r82	UTSW	7	12,039,205 (GRCm39)	missense	probably damaging	1.00
R6180:Vmn1r82	UTSW	7	12,039,012 (GRCm39)	missense	probably damaging	0.97
R6263:Vmn1r82	UTSW	7	12,039,461 (GRCm39)	missense	probably damaging	1.00
R6877:Vmn1r82	UTSW	7	12,039,290 (GRCm39)	missense	possibly damaging	0.79
R9551:Vmn1r82	UTSW	7	12,039,600 (GRCm39)	missense	possibly damaging	0.69
R9552:Vmn1r82	UTSW	7	12,039,600 (GRCm39)	missense	possibly damaging	0.69
R9792:Vmn1r82	UTSW	7	12,039,083 (GRCm39)	missense	probably benign	0.05

Posted On

2014-05-07