Mutagenetix > Incidental Mutation

Incidental Mutation 'R6901:Vmn1r74'

538526

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r74

Ensembl Gene

ENSMUSG00000047655

Gene Name

vomeronasal 1 receptor 74

Synonyms

V1rg5

MMRRC Submission

044995-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.062) question?

Stock #

R6901 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

11580702-11581616 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 11581368 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 223 (F223L)

Ref Sequence

ENSEMBL: ENSMUSP00000154746 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050416] [ENSMUST00000228471]

AlphaFold

Q8R290

Predicted Effect

probably benign
Transcript: ENSMUST00000050416
AA Change: F223L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

SMART Domains

Protein: ENSMUSP00000055148
Gene: ENSMUSG00000047655
AA Change: F223L

Domain	Start	End	E-Value	Type
Pfam:7tm_1	22	290	1.3e-7	PFAM
Pfam:V1R	34	296	1.2e-31	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000228471
AA Change: F223L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.3%
20x: 97.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd5	T	A	9: 122,197,220 (GRCm39)	S136T	probably benign	Het
Anxa10	T	C	8: 62,549,816 (GRCm39)	T10A	probably damaging	Het
Ap3b1	A	G	13: 94,554,650 (GRCm39)	E262G	probably benign	Het
Ap3b2	T	C	7: 81,134,660 (GRCm39)		probably null	Het
Arhgef40	A	G	14: 52,234,825 (GRCm39)	T1043A	probably damaging	Het
Arhgef5	T	A	6: 43,250,232 (GRCm39)	S328T	probably benign	Het
Arid4a	A	G	12: 71,113,911 (GRCm39)	K166R	probably damaging	Het
Cdh12	A	G	15: 21,583,872 (GRCm39)	I571V	probably benign	Het
Cdh4	G	A	2: 179,501,987 (GRCm39)	V316I	probably benign	Het
Cebpg	A	T	7: 34,750,202 (GRCm39)	H20Q	probably benign	Het
Ces4a	G	A	8: 105,873,330 (GRCm39)	V392I	probably benign	Het
CN725425	C	A	15: 91,124,966 (GRCm39)	P169T	possibly damaging	Het
Cyp2c54	A	G	19: 40,058,703 (GRCm39)	F243S	probably damaging	Het
Dkk2	T	A	3: 131,880,887 (GRCm39)		probably null	Het
Dync2h1	A	G	9: 7,131,855 (GRCm39)	Y1651H	probably damaging	Het
Dyrk1b	T	A	7: 27,884,542 (GRCm39)	L346Q	probably damaging	Het
Ephx4	T	C	5: 107,561,427 (GRCm39)	V85A	probably benign	Het
Etv6	A	G	6: 134,243,421 (GRCm39)	E392G	probably benign	Het
Fli1	T	A	9: 32,341,221 (GRCm39)	N202I	probably benign	Het
Gpc6	G	T	14: 118,188,629 (GRCm39)	R421L	possibly damaging	Het
Gse1	A	G	8: 120,956,561 (GRCm39)		probably benign	Het
Hdac1-ps	A	G	17: 78,800,089 (GRCm39)	E360G	probably benign	Het
Hnrnpab	T	C	11: 51,492,675 (GRCm39)		probably benign	Het
Hyal4	A	G	6: 24,756,190 (GRCm39)	E136G	probably damaging	Het
Ift56	G	A	6: 38,378,079 (GRCm39)	R297H	possibly damaging	Het
Kcna3	C	T	3: 106,943,884 (GRCm39)	A49V	probably benign	Het
Krt42	C	T	11: 100,160,542 (GRCm39)	M52I	probably benign	Het
Lyrm4	A	T	13: 36,301,107 (GRCm39)	Y13N	probably damaging	Het
Map2	C	T	1: 66,460,932 (GRCm39)	S1576L	possibly damaging	Het
Map3k12	G	T	15: 102,409,064 (GRCm39)	P817Q	possibly damaging	Het
Map3k12	G	T	15: 102,409,065 (GRCm39)	P817T	possibly damaging	Het
Masp1	T	C	16: 23,332,584 (GRCm39)	K84E	probably damaging	Het
Mki67	A	T	7: 135,310,489 (GRCm39)		probably null	Het
Mrap	C	G	16: 90,546,193 (GRCm39)	S94C	probably damaging	Het
Mybpc2	C	A	7: 44,154,779 (GRCm39)	C986F	probably damaging	Het
Nbea	A	C	3: 55,926,836 (GRCm39)	M789R	probably damaging	Het
Or2ag1b	T	C	7: 106,288,396 (GRCm39)	I181V	probably benign	Het
Or6b2	G	T	1: 92,408,327 (GRCm39)	N5K	probably damaging	Het
Pde4a	A	G	9: 21,116,266 (GRCm39)	N475S	probably benign	Het
Pex7	C	T	10: 19,736,740 (GRCm39)	V297I	probably benign	Het
Pkd1l3	A	T	8: 110,341,246 (GRCm39)	H33L	unknown	Het
Prl8a6	A	T	13: 27,621,030 (GRCm39)	Y67N	possibly damaging	Het
Rcor1	A	T	12: 111,075,322 (GRCm39)	E383V	probably damaging	Het
Slc22a27	A	T	19: 7,903,944 (GRCm39)	S64R	probably damaging	Het
Snx7	G	A	3: 117,623,285 (GRCm39)	Q292*	probably null	Het
Tgm3	C	T	2: 129,883,890 (GRCm39)	T516M	possibly damaging	Het
Trim9	T	C	12: 70,393,413 (GRCm39)	E177G	probably damaging	Het
Ttc28	C	A	5: 111,424,891 (GRCm39)	T1541N	possibly damaging	Het
Ttc8	T	A	12: 98,927,735 (GRCm39)	L202H	probably damaging	Het
Ttll13	T	C	7: 79,899,930 (GRCm39)	Y90H	probably damaging	Het
Uba1y	T	G	Y: 825,496 (GRCm39)	I286S	probably benign	Het
Ubxn11	G	A	4: 133,853,575 (GRCm39)	A125T	probably damaging	Het
Vmn1r48	A	G	6: 90,013,550 (GRCm39)	Y92H	possibly damaging	Het
Vwa5b1	G	A	4: 138,313,880 (GRCm39)	T696I	probably benign	Het
Zfp266	G	T	9: 20,410,895 (GRCm39)	Y427*	probably null	Het
Zfp362	C	T	4: 128,679,808 (GRCm39)	C273Y	probably damaging	Het
Zfp385c	T	C	11: 100,523,585 (GRCm39)	N123S	probably benign	Het
Zfp936	T	A	7: 42,839,467 (GRCm39)	H311Q	probably damaging	Het

Other mutations in Vmn1r74

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01608:Vmn1r74	APN	7	11,581,560 (GRCm39)	missense	probably damaging	0.98
IGL01673:Vmn1r74	APN	7	11,581,317 (GRCm39)	missense	possibly damaging	0.94
IGL03023:Vmn1r74	APN	7	11,581,257 (GRCm39)	missense	possibly damaging	0.46
IGL03409:Vmn1r74	APN	7	11,581,240 (GRCm39)	missense	probably damaging	0.99
R0393:Vmn1r74	UTSW	7	11,581,242 (GRCm39)	missense	possibly damaging	0.79
R1488:Vmn1r74	UTSW	7	11,581,510 (GRCm39)	missense	probably benign	0.02
R1707:Vmn1r74	UTSW	7	11,581,504 (GRCm39)	missense	probably damaging	0.98
R1998:Vmn1r74	UTSW	7	11,581,302 (GRCm39)	missense	probably damaging	1.00
R1999:Vmn1r74	UTSW	7	11,581,302 (GRCm39)	missense	probably damaging	1.00
R2139:Vmn1r74	UTSW	7	11,581,243 (GRCm39)	missense	probably damaging	1.00
R4027:Vmn1r74	UTSW	7	11,580,898 (GRCm39)	missense	probably damaging	0.98
R4576:Vmn1r74	UTSW	7	11,580,696 (GRCm39)	splice site	probably null
R4619:Vmn1r74	UTSW	7	11,581,403 (GRCm39)	missense	probably damaging	1.00
R4619:Vmn1r74	UTSW	7	11,581,398 (GRCm39)	missense	possibly damaging	0.61
R5371:Vmn1r74	UTSW	7	11,580,984 (GRCm39)	missense	probably damaging	1.00
R5606:Vmn1r74	UTSW	7	11,580,822 (GRCm39)	missense	probably benign	0.01
R6464:Vmn1r74	UTSW	7	11,581,131 (GRCm39)	missense	possibly damaging	0.87
R6920:Vmn1r74	UTSW	7	11,581,575 (GRCm39)	missense	probably benign	0.01
R7223:Vmn1r74	UTSW	7	11,580,894 (GRCm39)	nonsense	probably null
R7231:Vmn1r74	UTSW	7	11,580,888 (GRCm39)	missense	probably benign	0.34
R7418:Vmn1r74	UTSW	7	11,581,081 (GRCm39)	missense	possibly damaging	0.88
R8135:Vmn1r74	UTSW	7	11,581,530 (GRCm39)	missense	probably benign	0.36
R8692:Vmn1r74	UTSW	7	11,580,972 (GRCm39)	missense	probably benign	0.03
R8748:Vmn1r74	UTSW	7	11,580,903 (GRCm39)	missense	probably benign	0.10
R9004:Vmn1r74	UTSW	7	11,580,840 (GRCm39)	missense	probably benign	0.00
R9258:Vmn1r74	UTSW	7	11,580,999 (GRCm39)	missense	possibly damaging	0.86
R9564:Vmn1r74	UTSW	7	11,581,534 (GRCm39)	missense	probably damaging	1.00
RF049:Vmn1r74	UTSW	7	11,581,067 (GRCm39)	frame shift	probably null
RF063:Vmn1r74	UTSW	7	11,581,067 (GRCm39)	frame shift	probably null
Z1176:Vmn1r74	UTSW	7	11,580,936 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AACAGGATGCATCTTGGGTAC -3'
(R):5'- GACCTAGACTTCATGCTGCTG -3'

Sequencing Primer
(F):5'- ACAGGATGCATCTTGGGTACTGTTC -3'
(R):5'- ACCTAGACTTCATGCTGCTGATGAG -3'

Posted On

2018-11-06