Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01363:Vmn1r119'

75809

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn1r119

Ensembl Gene

ENSMUSG00000094010

Gene Name

vomeronasal 1 receptor 119

Synonyms

Gm1447, LOC384696

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01363

Quality Score

Status

Chromosome

Chromosomal Location

20745457-20746380 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 20746056 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 109 (V109I)

Ref Sequence

ENSEMBL: ENSMUSP00000127126 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164683]

AlphaFold

E9Q4H3

Predicted Effect

probably benign
Transcript: ENSMUST00000164683
AA Change: V109I

PolyPhen 2 Score 0.411 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000127126
Gene: ENSMUSG00000094010
AA Change: V109I

Domain	Start	End	E-Value	Type
Pfam:TAS2R	8	298	7.4e-17	PFAM
Pfam:7tm_1	31	290	2.1e-7	PFAM
Pfam:V1R	41	298	2e-18	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3100002H09Rik	A	G	4: 124,504,483 (GRCm39)	F23S	probably damaging	Het
Abcg3	A	G	5: 105,096,228 (GRCm39)	V528A	possibly damaging	Het
Adgrv1	A	G	13: 81,705,184 (GRCm39)	V1542A	probably damaging	Het
Alkbh3	A	G	2: 93,833,396 (GRCm39)		probably null	Het
Ang4	G	T	14: 52,001,636 (GRCm39)	T104K	probably benign	Het
Arhgef3	T	A	14: 27,123,876 (GRCm39)	C532*	probably null	Het
Bnip3	G	A	7: 138,499,777 (GRCm39)	T70I	probably benign	Het
Cast	T	C	13: 74,852,311 (GRCm39)	E644G	possibly damaging	Het
Cenpc1	A	T	5: 86,194,390 (GRCm39)	C125*	probably null	Het
Crb2	C	A	2: 37,683,845 (GRCm39)	R1116S	probably benign	Het
Cyp2c67	T	G	19: 39,628,411 (GRCm39)	I178L	probably damaging	Het
Cyp2c68	T	A	19: 39,691,871 (GRCm39)	M351L	probably benign	Het
Dusp1	G	A	17: 26,725,264 (GRCm39)	P365L	probably damaging	Het
Gatb	T	C	3: 85,559,652 (GRCm39)	L492P	probably damaging	Het
Igkv8-19	T	C	6: 70,318,083 (GRCm39)	S48G	probably damaging	Het
Isyna1	G	A	8: 71,047,372 (GRCm39)	V32I	probably damaging	Het
Itgb6	T	A	2: 60,441,726 (GRCm39)	N695Y	possibly damaging	Het
Klra8	T	C	6: 130,092,561 (GRCm39)	T247A	probably benign	Het
Mak	G	A	13: 41,206,853 (GRCm39)		probably benign	Het
Minar2	G	A	18: 59,205,380 (GRCm39)	G98D	probably damaging	Het
Mndal	T	A	1: 173,685,022 (GRCm39)	T516S	possibly damaging	Het
Mphosph9	G	T	5: 124,400,084 (GRCm39)	T939K	probably damaging	Het
Nfrkb	A	G	9: 31,325,667 (GRCm39)	T1037A	possibly damaging	Het
Or2m13	C	T	16: 19,226,333 (GRCm39)	M145I	probably benign	Het
Or8c9	A	G	9: 38,240,999 (GRCm39)	T39A	probably benign	Het
Pard3b	A	G	1: 62,676,799 (GRCm39)	Y1011C	probably damaging	Het
Parm1	G	A	5: 91,760,877 (GRCm39)	V250M	probably damaging	Het
Pgap2	T	G	7: 101,875,489 (GRCm39)	M1R	probably null	Het
Phlpp2	T	C	8: 110,663,729 (GRCm39)	F923L	probably benign	Het
Polr1a	T	A	6: 71,925,470 (GRCm39)	M739K	probably benign	Het
Pramel1	A	G	4: 143,123,955 (GRCm39)	Y210C	probably benign	Het
Pramel27	A	T	4: 143,579,846 (GRCm39)	Y477F	probably benign	Het
Raver2	A	G	4: 100,977,780 (GRCm39)		probably benign	Het
Rb1cc1	C	T	1: 6,320,333 (GRCm39)	L1251F	probably benign	Het
Ros1	T	A	10: 52,042,238 (GRCm39)	Y238F	probably damaging	Het
Shroom3	T	C	5: 93,088,852 (GRCm39)	L534P	probably benign	Het
Tjp1	A	T	7: 64,952,713 (GRCm39)	F1540L	possibly damaging	Het
Tmem200b	C	A	4: 131,649,704 (GRCm39)	P208Q	probably benign	Het
Tmem236	T	C	2: 14,179,441 (GRCm39)	L14P	probably damaging	Het
Tubgcp6	A	T	15: 88,991,728 (GRCm39)	I623N	probably damaging	Het
Vmn2r98	A	G	17: 19,286,020 (GRCm39)	N173D	probably benign	Het

Other mutations in Vmn1r119

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02218:Vmn1r119	APN	7	20,745,561 (GRCm39)	missense	probably benign	0.11
R0639:Vmn1r119	UTSW	7	20,745,593 (GRCm39)	missense	possibly damaging	0.70
R1844:Vmn1r119	UTSW	7	20,746,121 (GRCm39)	missense	probably damaging	1.00
R2250:Vmn1r119	UTSW	7	20,746,184 (GRCm39)	missense	probably damaging	1.00
R2927:Vmn1r119	UTSW	7	20,746,056 (GRCm39)	missense	probably benign	0.41
R4279:Vmn1r119	UTSW	7	20,745,786 (GRCm39)	missense	probably benign	0.00
R5022:Vmn1r119	UTSW	7	20,746,245 (GRCm39)	missense	probably benign	0.08
R6160:Vmn1r119	UTSW	7	20,745,740 (GRCm39)	missense	possibly damaging	0.47
R6523:Vmn1r119	UTSW	7	20,745,777 (GRCm39)	missense	possibly damaging	0.75
R7013:Vmn1r119	UTSW	7	20,745,714 (GRCm39)	missense	probably damaging	1.00
R7218:Vmn1r119	UTSW	7	20,745,572 (GRCm39)	missense	probably benign	0.00
R7320:Vmn1r119	UTSW	7	20,746,271 (GRCm39)	missense	probably damaging	0.99
R8233:Vmn1r119	UTSW	7	20,745,932 (GRCm39)	missense	probably damaging	0.99
R8550:Vmn1r119	UTSW	7	20,745,980 (GRCm39)	missense	probably benign	0.00
R9151:Vmn1r119	UTSW	7	20,745,593 (GRCm39)	missense	possibly damaging	0.70
R9300:Vmn1r119	UTSW	7	20,745,638 (GRCm39)	missense	probably damaging	1.00
R9343:Vmn1r119	UTSW	7	20,746,358 (GRCm39)	missense	probably benign	0.03
R9345:Vmn1r119	UTSW	7	20,746,034 (GRCm39)	missense	probably damaging	0.99
R9661:Vmn1r119	UTSW	7	20,746,224 (GRCm39)	missense	possibly damaging	0.87
X0060:Vmn1r119	UTSW	7	20,746,208 (GRCm39)	missense	possibly damaging	0.79
Z1177:Vmn1r119	UTSW	7	20,745,705 (GRCm39)	missense	probably benign	0.02

Posted On

2013-10-07