Mutagenetix > Incidental Mutation

Incidental Mutation 'R7608:Vmn1r53'

588434

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r53

Ensembl Gene

ENSMUSG00000057697

Gene Name

vomeronasal 1 receptor 53

Synonyms

VN5, V1rb3

MMRRC Submission

045678-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R7608 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

90200299-90201420 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 90201104 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 73 (M73I)

Ref Sequence

ENSEMBL: ENSMUSP00000075455 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076086]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000076086
AA Change: M73I

PolyPhen 2 Score 0.040 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000075455
Gene: ENSMUSG00000057697
AA Change: M73I

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
Pfam:V1R	38	302	1.4e-138	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

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

Validation Efficiency

100% (51/51)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb6	A	G	1: 75,154,347 (GRCm39)	F311S	probably benign	Het
Adamts7	C	A	9: 90,055,826 (GRCm39)	T193N	possibly damaging	Het
Akr1b7	A	G	6: 34,397,457 (GRCm39)	N273S	probably damaging	Het
Asz1	G	A	6: 18,077,252 (GRCm39)	T151M	probably damaging	Het
Atosb	A	G	4: 43,036,533 (GRCm39)	L66P	probably damaging	Het
Atrnl1	T	A	19: 57,703,119 (GRCm39)	Y1046N	probably damaging	Het
Cacna2d1	T	C	5: 16,564,022 (GRCm39)	S902P	probably damaging	Het
Casp3	T	A	8: 47,087,368 (GRCm39)	I105K	probably benign	Het
Ccdc146	C	T	5: 21,506,450 (GRCm39)	V664I	probably benign	Het
Cfap61	G	A	2: 145,805,451 (GRCm39)	C267Y	possibly damaging	Het
Dgkz	A	T	2: 91,764,399 (GRCm39)		probably null	Het
Dnah11	G	T	12: 118,104,505 (GRCm39)		probably null	Het
Duox1	C	A	2: 122,156,616 (GRCm39)	Y514*	probably null	Het
Epha7	C	T	4: 28,871,937 (GRCm39)	S422L	probably benign	Het
Fan1	A	T	7: 64,003,979 (GRCm39)		probably null	Het
Fgfrl1	A	T	5: 108,853,211 (GRCm39)	K278M	probably damaging	Het
Fign	T	C	2: 63,809,063 (GRCm39)	I736V	possibly damaging	Het
Galns	A	G	8: 123,318,184 (GRCm39)	F410S	probably benign	Het
Hspbp1	C	A	7: 4,663,821 (GRCm39)	K341N	possibly damaging	Het
Idh3b	A	T	2: 130,122,900 (GRCm39)	S296R	probably damaging	Het
Ifi44	A	G	3: 151,438,045 (GRCm39)	F414S	probably damaging	Het
Kdm3a	T	A	6: 71,577,731 (GRCm39)	M690L	probably benign	Het
Ldaf1	A	G	7: 119,704,011 (GRCm39)	K19E	probably damaging	Het
Lrrc49	C	T	9: 60,510,005 (GRCm39)	G488S	probably null	Het
Mcc	T	C	18: 44,624,294 (GRCm39)	N417S	possibly damaging	Het
Melk	T	A	4: 44,325,571 (GRCm39)		probably null	Het
Mtcl1	T	C	17: 66,650,300 (GRCm39)	R1722G	probably damaging	Het
Or4a79	A	G	2: 89,551,642 (GRCm39)	V271A	probably benign	Het
Or51f23c-ps1	A	G	7: 102,431,132 (GRCm39)	I150V	probably benign	Het
Or5b119	G	A	19: 13,456,956 (GRCm39)	T202I	possibly damaging	Het
Or8d2	T	A	9: 38,759,806 (GRCm39)	V132D	possibly damaging	Het
Pdzrn3	T	C	6: 101,128,713 (GRCm39)	E651G	probably damaging	Het
Pop5	A	G	5: 115,375,931 (GRCm39)		probably benign	Het
Prox1	T	A	1: 189,885,642 (GRCm39)	M602L	probably benign	Het
Prpf39	G	A	12: 65,100,220 (GRCm39)	A298T	probably benign	Het
Scg2	T	C	1: 79,413,898 (GRCm39)	E275G	probably benign	Het
Scn11a	A	T	9: 119,644,379 (GRCm39)		probably null	Het
Slc16a4	A	T	3: 107,210,443 (GRCm39)	Y371F	probably damaging	Het
Slc4a1ap	T	A	5: 31,693,533 (GRCm39)	M489K	possibly damaging	Het
Spata13	A	G	14: 60,929,956 (GRCm39)	N505D	possibly damaging	Het
Tas2r129	A	G	6: 132,928,156 (GRCm39)	N31S	probably damaging	Het
Tnn	A	T	1: 159,915,984 (GRCm39)	Y1508*	probably null	Het
Trim23	T	C	13: 104,328,541 (GRCm39)	V354A	probably benign	Het
Tsc1	A	T	2: 28,548,748 (GRCm39)	T18S	probably benign	Het
Txlnb	A	G	10: 17,691,146 (GRCm39)	K232R	probably damaging	Het
Vmn1r67	G	A	7: 10,181,290 (GRCm39)	V185M	possibly damaging	Het
Vmn2r14	A	G	5: 109,369,276 (GRCm39)	I99T	probably benign	Het
Zfp318	T	G	17: 46,710,935 (GRCm39)	V886G	probably damaging	Het
Zfp760	A	G	17: 21,941,797 (GRCm39)	N324S	probably benign	Het
Zfp819	T	C	7: 43,266,357 (GRCm39)	V280A	probably benign	Het

Other mutations in Vmn1r53

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03104:Vmn1r53	APN	6	90,200,944 (GRCm39)	nonsense	probably null
R0087:Vmn1r53	UTSW	6	90,200,413 (GRCm39)	missense	probably benign	0.03
R0240:Vmn1r53	UTSW	6	90,200,925 (GRCm39)	missense	probably damaging	1.00
R0240:Vmn1r53	UTSW	6	90,200,925 (GRCm39)	missense	probably damaging	1.00
R0361:Vmn1r53	UTSW	6	90,201,064 (GRCm39)	missense	possibly damaging	0.94
R0481:Vmn1r53	UTSW	6	90,200,700 (GRCm39)	missense	probably damaging	0.99
R1293:Vmn1r53	UTSW	6	90,201,196 (GRCm39)	missense	possibly damaging	0.69
R1464:Vmn1r53	UTSW	6	90,200,914 (GRCm39)	missense	probably benign	0.26
R1464:Vmn1r53	UTSW	6	90,200,914 (GRCm39)	missense	probably benign	0.26
R1901:Vmn1r53	UTSW	6	90,201,268 (GRCm39)	missense	possibly damaging	0.95
R2508:Vmn1r53	UTSW	6	90,200,554 (GRCm39)	missense	probably benign	0.00
R5428:Vmn1r53	UTSW	6	90,200,395 (GRCm39)	missense	probably benign	0.01
R5649:Vmn1r53	UTSW	6	90,200,742 (GRCm39)	missense	probably benign	0.00
R6365:Vmn1r53	UTSW	6	90,201,241 (GRCm39)	missense	probably damaging	1.00
R7410:Vmn1r53	UTSW	6	90,200,700 (GRCm39)	missense	probably damaging	0.99
R7673:Vmn1r53	UTSW	6	90,200,625 (GRCm39)	missense	probably damaging	1.00
R7951:Vmn1r53	UTSW	6	90,201,132 (GRCm39)	missense	possibly damaging	0.88
R8492:Vmn1r53	UTSW	6	90,200,394 (GRCm39)	missense	possibly damaging	0.82
R8936:Vmn1r53	UTSW	6	90,200,571 (GRCm39)	missense	probably benign	0.45
R8995:Vmn1r53	UTSW	6	90,200,757 (GRCm39)	missense	probably benign	0.22
Z1177:Vmn1r53	UTSW	6	90,201,093 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TCTAAGGTCAAATTGGGGTAAGC -3'
(R):5'- ACCTTATTCTCTGAAGTGAGTGTTG -3'

Sequencing Primer
(F):5'- GTCAAATTGGGGTAAGCAATAATTG -3'
(R):5'- GTTGGGATCTCAGCTAACAGTATCC -3'

Posted On

2019-10-24