Mutagenetix > Incidental Mutation

Incidental Mutation 'R7494:Vmn2r44'

580983

Institutional Source

Beutler Lab

Gene Symbol

Vmn2r44

Ensembl Gene

ENSMUSG00000094098

Gene Name

vomeronasal 2, receptor 44

Synonyms

EG434113

Accession Numbers

Essential gene?

Not available question?

Stock #

R7494 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

8370459-8386237 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 8386122 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Stop codon at position 39 (L39*)

Ref Sequence

ENSEMBL: ENSMUSP00000132467 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166499]

AlphaFold

L7N2E1

Predicted Effect

probably null
Transcript: ENSMUST00000166499
AA Change: L39*

SMART Domains

Protein: ENSMUSP00000132467
Gene: ENSMUSG00000094098
AA Change: L39*

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	73	469	2.5e-34	PFAM
Pfam:NCD3G	512	565	3.8e-20	PFAM
Pfam:7tm_3	598	833	5.7e-55	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca6	G	A	11: 110,099,571 (GRCm39)	T992I	possibly damaging	Het
Adamts10	T	A	17: 33,768,352 (GRCm39)	C841*	probably null	Het
AI661453	C	T	17: 47,779,105 (GRCm39)	P944S	unknown	Het
Als2	G	A	1: 59,222,325 (GRCm39)		probably null	Het
Anapc2	A	G	2: 25,166,376 (GRCm39)	E381G	possibly damaging	Het
Ank3	T	C	10: 69,824,756 (GRCm39)	Y1142H		Het
Apip	A	T	2: 102,922,896 (GRCm39)	N238I	probably benign	Het
Cblc	A	T	7: 19,526,737 (GRCm39)	V165D	possibly damaging	Het
Cep295nl	T	A	11: 118,224,758 (GRCm39)	M29L	probably benign	Het
Clec12a	A	G	6: 129,330,362 (GRCm39)	I47V	possibly damaging	Het
Dpp9	T	C	17: 56,507,619 (GRCm39)	Y350C	probably damaging	Het
Enpp2	C	T	15: 54,773,554 (GRCm39)	G56R	probably damaging	Het
Epsti1	G	T	14: 78,166,194 (GRCm39)	E82D	probably benign	Het
Eri2	C	A	7: 119,385,304 (GRCm39)	C399F	probably damaging	Het
Ern1	T	C	11: 106,298,361 (GRCm39)	T672A	probably damaging	Het
Fbxo21	T	A	5: 118,138,388 (GRCm39)	C445S	possibly damaging	Het
Folh1	G	T	7: 86,368,907 (GRCm39)	T740K	probably damaging	Het
Gapt	A	G	13: 110,490,262 (GRCm39)	Y134H	probably damaging	Het
Gm19410	T	C	8: 36,262,684 (GRCm39)	S874P	probably damaging	Het
Gm2431	G	A	7: 141,811,547 (GRCm39)	P119L	unknown	Het
Gzmc	G	A	14: 56,469,785 (GRCm39)	Q172*	probably null	Het
Hoxa1	C	A	6: 52,134,571 (GRCm39)	V211F	probably damaging	Het
Hyou1	G	T	9: 44,300,706 (GRCm39)	R925L	probably benign	Het
Ift70a1	A	C	2: 75,810,242 (GRCm39)	F614V	probably damaging	Het
Ilvbl	A	G	10: 78,414,857 (GRCm39)	Y240C	possibly damaging	Het
Lama1	T	A	17: 68,118,441 (GRCm39)	F2551Y		Het
Lrrtm3	A	G	10: 63,924,958 (GRCm39)	Y70H	probably damaging	Het
Naa38	T	A	11: 69,287,126 (GRCm39)	C69S	probably damaging	Het
Or12e7	T	A	2: 87,287,912 (GRCm39)	N134K	probably damaging	Het
Or2t46	T	C	11: 58,472,038 (GRCm39)	S123P	probably damaging	Het
Or8k25	A	T	2: 86,243,592 (GRCm39)	I268N	probably benign	Het
Panx3	A	G	9: 37,572,608 (GRCm39)	L314P	probably damaging	Het
Polr2f	T	C	15: 79,028,865 (GRCm39)		probably null	Het
Prkcd	C	A	14: 30,331,150 (GRCm39)	R75L	probably benign	Het
Psap	A	C	10: 60,135,275 (GRCm39)	L313F	probably benign	Het
Psen1	T	A	12: 83,775,017 (GRCm39)	C263S	probably benign	Het
Ptma	GGAAGAAG	GGAAGAAGAAG	1: 86,457,261 (GRCm39)		probably benign	Het
Pura	T	A	18: 36,420,942 (GRCm39)	M243K	probably damaging	Het
Sec16b	T	C	1: 157,388,369 (GRCm39)	S579P	probably benign	Het
Septin1	T	A	7: 126,814,122 (GRCm39)	E338V	probably damaging	Het
Sgms1	A	G	19: 32,107,091 (GRCm39)	F255L	probably benign	Het
Slc4a2	A	G	5: 24,637,862 (GRCm39)	T353A	possibly damaging	Het
Smg6	T	C	11: 74,820,449 (GRCm39)	V240A	probably benign	Het
Sntg2	T	G	12: 30,279,633 (GRCm39)	D340A	possibly damaging	Het
Sun1	C	T	5: 139,221,475 (GRCm39)	P553S	probably benign	Het
Tas2r140	T	C	6: 40,468,254 (GRCm39)	V28A	probably damaging	Het
Tfcp2l1	T	C	1: 118,592,686 (GRCm39)	F323S	probably damaging	Het
Thoc2l	T	C	5: 104,666,284 (GRCm39)	Y269H	possibly damaging	Het
Tpcn2	G	A	7: 144,832,586 (GRCm39)	T90I	possibly damaging	Het
Ttn	A	T	2: 76,720,321 (GRCm39)	Y6968*	probably null	Het

Other mutations in Vmn2r44

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01650:Vmn2r44	APN	7	8,383,103 (GRCm39)	critical splice donor site	probably null
IGL01723:Vmn2r44	APN	7	8,380,915 (GRCm39)	missense	probably damaging	0.97
IGL01767:Vmn2r44	APN	7	8,383,237 (GRCm39)	missense	probably benign	0.00
IGL02161:Vmn2r44	APN	7	8,380,814 (GRCm39)	missense	possibly damaging	0.94
IGL02299:Vmn2r44	APN	7	8,380,815 (GRCm39)	missense	probably benign
IGL02418:Vmn2r44	APN	7	8,380,864 (GRCm39)	missense	probably damaging	1.00
IGL02829:Vmn2r44	APN	7	8,380,879 (GRCm39)	missense	possibly damaging	0.94
IGL02851:Vmn2r44	APN	7	8,386,050 (GRCm39)	missense	probably damaging	1.00
IGL03080:Vmn2r44	APN	7	8,386,244 (GRCm39)	utr 5 prime	probably benign
R1471:Vmn2r44	UTSW	7	8,380,882 (GRCm39)	missense	probably damaging	0.99
R1789:Vmn2r44	UTSW	7	8,383,122 (GRCm39)	missense	possibly damaging	0.64
R1932:Vmn2r44	UTSW	7	8,370,981 (GRCm39)	missense	probably benign	0.04
R2354:Vmn2r44	UTSW	7	8,373,639 (GRCm39)	missense	probably damaging	0.99
R4009:Vmn2r44	UTSW	7	8,380,987 (GRCm39)	missense	possibly damaging	0.82
R4130:Vmn2r44	UTSW	7	8,370,918 (GRCm39)	missense	probably damaging	1.00
R4790:Vmn2r44	UTSW	7	8,370,949 (GRCm39)	missense	probably damaging	1.00
R4854:Vmn2r44	UTSW	7	8,383,300 (GRCm39)	missense	possibly damaging	0.94
R4887:Vmn2r44	UTSW	7	8,380,985 (GRCm39)	missense	probably benign	0.19
R4888:Vmn2r44	UTSW	7	8,380,985 (GRCm39)	missense	probably benign	0.19
R5484:Vmn2r44	UTSW	7	8,383,123 (GRCm39)	missense	possibly damaging	0.69
R6110:Vmn2r44	UTSW	7	8,381,005 (GRCm39)	missense	probably damaging	1.00
R6357:Vmn2r44	UTSW	7	8,373,657 (GRCm39)	missense	probably benign	0.01
R6526:Vmn2r44	UTSW	7	8,381,098 (GRCm39)	missense	probably benign	0.01
R7083:Vmn2r44	UTSW	7	8,381,369 (GRCm39)	missense	probably benign	0.44
R7087:Vmn2r44	UTSW	7	8,381,366 (GRCm39)	missense	probably benign	0.02
R7115:Vmn2r44	UTSW	7	8,370,527 (GRCm39)	nonsense	probably null
R7125:Vmn2r44	UTSW	7	8,370,941 (GRCm39)	missense	probably damaging	1.00
R7258:Vmn2r44	UTSW	7	8,380,848 (GRCm39)	missense	probably damaging	1.00
R7359:Vmn2r44	UTSW	7	8,370,538 (GRCm39)	missense	probably benign	0.30
R7766:Vmn2r44	UTSW	7	8,371,219 (GRCm39)	missense	probably damaging	1.00
R7777:Vmn2r44	UTSW	7	8,381,314 (GRCm39)	missense	possibly damaging	0.81
R8184:Vmn2r44	UTSW	7	8,371,227 (GRCm39)	nonsense	probably null
R8674:Vmn2r44	UTSW	7	8,380,822 (GRCm39)	missense	probably damaging	1.00
R8752:Vmn2r44	UTSW	7	8,370,805 (GRCm39)	missense	probably damaging	1.00
R8897:Vmn2r44	UTSW	7	8,381,242 (GRCm39)	missense	probably damaging	1.00
R8915:Vmn2r44	UTSW	7	8,370,650 (GRCm39)	missense	probably damaging	1.00
R8928:Vmn2r44	UTSW	7	8,381,101 (GRCm39)	missense	probably damaging	1.00
R9163:Vmn2r44	UTSW	7	8,371,091 (GRCm39)	missense	probably benign	0.00
Z1177:Vmn2r44	UTSW	7	8,370,976 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- CTTGGTGTTCAGACTTAGCAACAG -3'
(R):5'- TGCAATAAACCTCACCTTTGC -3'

Sequencing Primer
(F):5'- TGTTCAGACTTAGCAACAGGACAG -3'
(R):5'- TGCAAGGAGAAATTTGATGTACTG -3'

Posted On

2019-10-17