Mutagenetix > Incidental Mutation

Incidental Mutation 'R8979:Vmn1r174'

683633

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r174

Ensembl Gene

ENSMUSG00000090411

Gene Name

vomeronasal 1 receptor 174

Synonyms

V1rd22

MMRRC Submission

068812-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R8979 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

23453336-23454277 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 23453892 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 186 (V186D)

Ref Sequence

ENSEMBL: ENSMUSP00000126478 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000167551] [ENSMUST00000228331]

AlphaFold

E9PYW5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000167551
AA Change: V186D

PolyPhen 2 Score 0.916 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000126478
Gene: ENSMUSG00000090411
AA Change: V186D

Domain	Start	End	E-Value	Type
Pfam:TAS2R	8	300	4e-9	PFAM
Pfam:V1R	43	300	5e-19	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000228331
AA Change: V186D

PolyPhen 2 Score 0.916 (Sensitivity: 0.81; Specificity: 0.94)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2	A	C	3: 59,932,545 (GRCm39)	R353S	probably damaging	Het
Ablim3	C	T	18: 61,982,397 (GRCm39)	V183I	probably benign	Het
Adgrb3	T	A	1: 25,527,115 (GRCm39)	Q607L	probably benign	Het
Adgrl1	A	G	8: 84,665,015 (GRCm39)	D1234G	probably benign	Het
Alms1	A	G	6: 85,598,009 (GRCm39)	Y945C	probably damaging	Het
Arhgef26	T	A	3: 62,246,969 (GRCm39)	W18R	possibly damaging	Het
Caskin1	G	T	17: 24,717,899 (GRCm39)	A229S	possibly damaging	Het
Celsr1	A	T	15: 85,847,340 (GRCm39)	S1466T	probably damaging	Het
Cftr	T	C	6: 18,227,947 (GRCm39)	Y380H	probably benign	Het
Ciapin1	A	T	8: 95,549,753 (GRCm39)	L301Q	probably damaging	Het
Clec1b	A	G	6: 129,380,537 (GRCm39)	E151G	probably benign	Het
Cngb1	G	A	8: 96,004,913 (GRCm39)		probably benign	Het
Cntln	T	A	4: 85,048,910 (GRCm39)	V240E	probably damaging	Het
Cog5	A	G	12: 31,840,894 (GRCm39)	T240A	probably benign	Het
Col5a3	G	A	9: 20,686,597 (GRCm39)	P1343S	unknown	Het
Cspp1	T	A	1: 10,134,630 (GRCm39)	S127T	probably benign	Het
Dnah9	T	G	11: 65,895,978 (GRCm39)	M2466L	probably benign	Het
Fbn2	C	T	18: 58,286,928 (GRCm39)	G244R	probably damaging	Het
Fbxw13	A	T	9: 109,013,197 (GRCm39)	W247R	probably damaging	Het
Gbp4	G	A	5: 105,267,248 (GRCm39)	T557M	probably benign	Het
Ide	G	A	19: 37,302,711 (GRCm39)	A133V		Het
Il2rb	C	A	15: 78,376,052 (GRCm39)		probably benign	Het
Itgb1	A	G	8: 129,448,951 (GRCm39)	E519G	probably benign	Het
Kifc1	A	G	17: 34,102,228 (GRCm39)	Y462H	possibly damaging	Het
Krt1	A	G	15: 101,755,340 (GRCm39)	F473S	probably benign	Het
Llgl1	C	T	11: 60,601,129 (GRCm39)	A689V	probably benign	Het
Lrrc37a	C	A	11: 103,393,833 (GRCm39)	V531L	possibly damaging	Het
Mid1	C	G	X: 168,768,003 (GRCm39)	P384A	probably benign	Het
Mid1	G	A	X: 168,768,009 (GRCm39)	A386T	probably benign	Het
Mms22l	C	T	4: 24,580,070 (GRCm39)	L760F	probably benign	Het
Mplkipl1	A	G	19: 61,164,169 (GRCm39)	Y89H	probably damaging	Het
Mst1r	C	T	9: 107,792,478 (GRCm39)	R951C	probably damaging	Het
Naalad2	G	A	9: 18,242,146 (GRCm39)	T586M	probably damaging	Het
Or4c108	C	T	2: 88,804,173 (GRCm39)	V21I	probably benign	Het
Oxct2b	A	G	4: 123,011,169 (GRCm39)	N363S	probably benign	Het
Padi6	T	G	4: 140,466,474 (GRCm39)	N145T	probably benign	Het
Plcl2	T	A	17: 50,947,145 (GRCm39)	M1008K	possibly damaging	Het
Plekha5	T	C	6: 140,496,818 (GRCm39)	S435P	probably damaging	Het
Prkacb	C	A	3: 146,518,411 (GRCm39)	G10C	probably benign	Het
Psg29	A	T	7: 16,937,544 (GRCm39)		probably benign	Het
Ptpn4	T	C	1: 119,671,120 (GRCm39)	T213A	probably damaging	Het
Ptpro	A	G	6: 137,345,140 (GRCm39)	I49V	probably benign	Het
Rassf1	A	G	9: 107,429,004 (GRCm39)	D70G	probably benign	Het
Rbm24	A	T	13: 46,572,531 (GRCm39)	T9S	probably damaging	Het
Rp1	T	C	1: 4,218,937 (GRCm39)	T948A	unknown	Het
Ryr2	A	T	13: 11,609,924 (GRCm39)	C4301S	probably benign	Het
S100pbp	T	C	4: 129,076,133 (GRCm39)	D64G	probably damaging	Het
Samd3	A	G	10: 26,120,428 (GRCm39)	K141E	possibly damaging	Het
Scgb1b29	A	T	7: 32,141,277 (GRCm39)	K65*	probably null	Het
Shoc1	T	C	4: 59,047,276 (GRCm39)	T1448A	possibly damaging	Het
Slc51b	T	C	9: 65,320,210 (GRCm39)	N86D	probably benign	Het
Slc6a3	G	A	13: 73,715,720 (GRCm39)	V452I	probably benign	Het
Sobp	A	G	10: 42,896,976 (GRCm39)		probably null	Het
Spats2	T	C	15: 99,110,123 (GRCm39)	S507P	possibly damaging	Het
Spns3	C	T	11: 72,420,416 (GRCm39)	A357T	probably damaging	Het
Suox	A	T	10: 128,507,367 (GRCm39)	H220Q	probably damaging	Het
Tbc1d9b	A	T	11: 50,061,809 (GRCm39)	S1106C	probably benign	Het
Tbx1	T	C	16: 18,406,745 (GRCm39)	D9G	unknown	Het
Tcaf2	A	T	6: 42,601,404 (GRCm39)	F885Y	probably damaging	Het
Tgoln1	T	C	6: 72,593,262 (GRCm39)	T73A	probably benign	Het
Tigd3	G	A	19: 5,941,853 (GRCm39)	P426S	probably benign	Het
Tmem233	T	A	5: 116,221,260 (GRCm39)		probably benign	Het
Tnfrsf11a	A	G	1: 105,754,825 (GRCm39)	D299G	possibly damaging	Het
Trim32	T	C	4: 65,531,692 (GRCm39)	V83A	possibly damaging	Het
Unc13a	A	T	8: 72,113,125 (GRCm39)	M242K	probably benign	Het
Vat1	C	T	11: 101,353,041 (GRCm39)	G293D	probably damaging	Het
Wdfy3	A	G	5: 102,096,764 (GRCm39)	Y345H	probably damaging	Het
Zzef1	C	T	11: 72,766,003 (GRCm39)	T1510I	probably benign	Het

Other mutations in Vmn1r174

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00331:Vmn1r174	APN	7	23,453,958 (GRCm39)	missense	possibly damaging	0.77
IGL00950:Vmn1r174	APN	7	23,453,911 (GRCm39)	missense	possibly damaging	0.96
IGL01484:Vmn1r174	APN	7	23,453,749 (GRCm39)	nonsense	probably null
IGL02014:Vmn1r174	APN	7	23,453,583 (GRCm39)	missense	probably damaging	1.00
IGL02190:Vmn1r174	APN	7	23,454,252 (GRCm39)	missense	unknown
IGL03265:Vmn1r174	APN	7	23,453,898 (GRCm39)	nonsense	probably null
IGL03335:Vmn1r174	APN	7	23,453,937 (GRCm39)	missense	probably benign	0.41
R0529:Vmn1r174	UTSW	7	23,453,622 (GRCm39)	missense	probably benign	0.00
R1489:Vmn1r174	UTSW	7	23,453,981 (GRCm39)	nonsense	probably null
R1645:Vmn1r174	UTSW	7	23,453,777 (GRCm39)	missense	possibly damaging	0.87
R1691:Vmn1r174	UTSW	7	23,453,337 (GRCm39)	start codon destroyed	probably null	1.00
R1753:Vmn1r174	UTSW	7	23,453,622 (GRCm39)	missense	probably benign	0.00
R1939:Vmn1r174	UTSW	7	23,453,532 (GRCm39)	missense	probably damaging	0.99
R1988:Vmn1r174	UTSW	7	23,454,050 (GRCm39)	missense	probably damaging	0.98
R2299:Vmn1r174	UTSW	7	23,453,429 (GRCm39)	missense	probably benign	0.08
R4429:Vmn1r174	UTSW	7	23,453,565 (GRCm39)	missense	probably benign	0.02
R4516:Vmn1r174	UTSW	7	23,453,768 (GRCm39)	missense	probably benign	0.01
R4589:Vmn1r174	UTSW	7	23,454,204 (GRCm39)	nonsense	probably null
R5175:Vmn1r174	UTSW	7	23,454,153 (GRCm39)	missense	probably benign	0.03
R5392:Vmn1r174	UTSW	7	23,454,227 (GRCm39)	missense	unknown
R5503:Vmn1r174	UTSW	7	23,453,562 (GRCm39)	missense	probably benign	0.03
R5568:Vmn1r174	UTSW	7	23,453,919 (GRCm39)	missense	probably damaging	0.96
R6705:Vmn1r174	UTSW	7	23,453,851 (GRCm39)	missense	probably benign	0.25
R8168:Vmn1r174	UTSW	7	23,454,096 (GRCm39)	missense	probably damaging	0.99
R8190:Vmn1r174	UTSW	7	23,453,568 (GRCm39)	missense	probably damaging	1.00
R8523:Vmn1r174	UTSW	7	23,454,182 (GRCm39)	missense	probably damaging	1.00
R8555:Vmn1r174	UTSW	7	23,453,970 (GRCm39)	missense	possibly damaging	0.84
R8913:Vmn1r174	UTSW	7	23,453,375 (GRCm39)	missense	possibly damaging	0.90
R8990:Vmn1r174	UTSW	7	23,453,956 (GRCm39)	missense	possibly damaging	0.71
X0011:Vmn1r174	UTSW	7	23,453,906 (GRCm39)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- ACTTGTATCCTGAGCTCTTACCAG -3'
(R):5'- TCAGCATGAGAATTGTGTTTGC -3'

Sequencing Primer
(F):5'- TCCTGGTAAATGGAGTAGAGTGATAC -3'
(R):5'- AGCATGAGAATTGTGTTTGCTGCTC -3'

Posted On

2021-10-11