Mutagenetix > Incidental Mutation

Incidental Mutation 'R7661:Vmn1r2'

591552

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r2

Ensembl Gene

ENSMUSG00000115072

Gene Name

vomeronasal 1 receptor 2

Synonyms

Gm11776

MMRRC Submission

045736-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.841) question?

Stock #

R7661 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

3172083-3173003 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 3172149 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Isoleucine at position 23 (F23I)

Ref Sequence

ENSEMBL: ENSMUSP00000100791 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000105160] [ENSMUST00000226198]

AlphaFold

A2AMT6

Predicted Effect

probably benign
Transcript: ENSMUST00000105160
AA Change: F23I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000100791
Gene: ENSMUSG00000115072
AA Change: F23I

Domain	Start	End	E-Value	Type
Pfam:TAS2R	7	302	2.7e-8	PFAM
Pfam:V1R	30	298	6.3e-33	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000226198
AA Change: F23I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

96% (50/52)

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110018I06Rik	A	T	12: 107,455,215 (GRCm39)	K100N	unknown	Het
Abi3bp	T	A	16: 56,453,263 (GRCm39)		probably null	Het
Akr1c20	T	C	13: 4,558,218 (GRCm39)	D210G	probably benign	Het
Arid5b	C	T	10: 67,934,417 (GRCm39)	G495E	probably benign	Het
Ascc1	A	C	10: 59,885,629 (GRCm39)	N227H	probably damaging	Het
Atp5f1a	G	T	18: 77,861,802 (GRCm39)	A18S	possibly damaging	Het
Bcl2l13	A	G	6: 120,842,558 (GRCm39)	T84A	possibly damaging	Het
Blmh	T	A	11: 76,877,341 (GRCm39)	V419D	probably damaging	Het
Cacna1d	G	A	14: 29,769,177 (GRCm39)	P1918S	probably benign	Het
Calr4	T	C	4: 109,110,951 (GRCm39)	V339A	probably benign	Het
Capza3	C	A	6: 139,987,498 (GRCm39)	D32E	probably benign	Het
Cilk1	G	C	9: 78,074,902 (GRCm39)	V586L	probably benign	Het
Cldn20	T	A	17: 3,583,133 (GRCm39)	M102K	possibly damaging	Het
Dennd1a	T	C	2: 37,734,841 (GRCm39)	Q479R	probably benign	Het
Dpp10	A	T	1: 123,312,681 (GRCm39)	I432N	probably damaging	Het
Dst	T	A	1: 34,295,434 (GRCm39)		probably null	Het
Efcab3	T	A	11: 104,617,503 (GRCm39)	D741E	probably benign	Het
Fam135a	C	T	1: 24,111,843 (GRCm39)		probably null	Het
Fam47e	C	T	5: 92,735,384 (GRCm39)	L206F	probably damaging	Het
Focad	G	A	4: 88,221,772 (GRCm39)	R714H	unknown	Het
Hace1	T	G	10: 45,481,649 (GRCm39)	V124G	probably damaging	Het
Ifit1bl2	T	A	19: 34,596,428 (GRCm39)	Y396F	probably damaging	Het
Il22ra2	A	G	10: 19,497,826 (GRCm39)	I13M	probably benign	Het
Kif21a	A	G	15: 90,865,122 (GRCm39)	F517L	possibly damaging	Het
Lrrc4	T	C	6: 28,829,762 (GRCm39)	T618A	probably benign	Het
Mdn1	A	G	4: 32,691,229 (GRCm39)	T952A	probably benign	Het
Mindy3	A	T	2: 12,402,328 (GRCm39)	I208K	probably damaging	Het
Mug1	C	A	6: 121,838,179 (GRCm39)	H470N	possibly damaging	Het
Mycbp2	A	G	14: 103,450,059 (GRCm39)	I1744T	probably damaging	Het
Nanog	A	T	6: 122,690,431 (GRCm39)	R279W	probably damaging	Het
Ncoa2	T	A	1: 13,244,761 (GRCm39)	T646S	probably damaging	Het
Ndufa5	A	G	6: 24,518,724 (GRCm39)	*117R	probably null	Het
Nudt18	A	T	14: 70,817,276 (GRCm39)	E293D	probably benign	Het
Or1e22	A	G	11: 73,377,426 (GRCm39)	S75P	probably damaging	Het
Or51aa2	A	T	7: 103,187,826 (GRCm39)	V205E	probably damaging	Het
Paip1	C	T	13: 119,587,306 (GRCm39)	T390I	possibly damaging	Het
Pigg	G	A	5: 108,486,485 (GRCm39)	V713I	probably benign	Het
Pih1d2	T	C	9: 50,529,558 (GRCm39)		probably null	Het
Ppp2r3d	A	G	9: 124,442,696 (GRCm38)	F17L		Het
Ptprk	T	C	10: 28,342,036 (GRCm39)	I481T	probably benign	Het
Pygo2	T	C	3: 89,338,038 (GRCm39)		probably null	Het
Raet1d	T	C	10: 22,248,156 (GRCm39)	S225P	possibly damaging	Het
Rnf24	T	C	2: 131,164,135 (GRCm39)		probably benign	Het
Ror1	A	G	4: 100,298,687 (GRCm39)	S687G	probably damaging	Het
Rsph9	A	G	17: 46,446,013 (GRCm39)	S186P	probably damaging	Het
Sash1	C	T	10: 8,605,155 (GRCm39)	M1078I	probably benign	Het
Scd4	C	A	19: 44,327,510 (GRCm39)	D195E	probably benign	Het
Spopfm3	C	T	3: 94,105,709 (GRCm39)	T9I	probably damaging	Het
Syn3	A	G	10: 85,904,940 (GRCm39)	C348R	probably damaging	Het
Uspl1	T	C	5: 149,151,827 (GRCm39)	F1009S	probably benign	Het
Vmn1r257	A	G	7: 22,391,229 (GRCm39)	S172P	probably benign	Het
Vmn2r-ps158	T	A	7: 42,672,582 (GRCm39)	N72K	probably benign	Het
Zfp747l1	A	T	7: 126,984,135 (GRCm39)	C322*	probably null	Het
Zfp839	C	T	12: 110,835,226 (GRCm39)	T827I	probably benign	Het

Other mutations in Vmn1r2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00328:Vmn1r2	APN	4	3,172,807 (GRCm39)	missense	probably damaging	0.98
PIT4151001:Vmn1r2	UTSW	4	3,172,623 (GRCm39)	missense	probably benign	0.00
PIT4354001:Vmn1r2	UTSW	4	3,172,162 (GRCm39)	missense	probably benign	0.23
R1836:Vmn1r2	UTSW	4	3,172,836 (GRCm39)	missense	probably damaging	1.00
R1855:Vmn1r2	UTSW	4	3,172,588 (GRCm39)	missense	probably damaging	1.00
R2319:Vmn1r2	UTSW	4	3,172,083 (GRCm39)	start codon destroyed	probably null	0.02
R3414:Vmn1r2	UTSW	4	3,172,696 (GRCm39)	missense	probably damaging	1.00
R3824:Vmn1r2	UTSW	4	3,172,413 (GRCm39)	missense	probably damaging	1.00
R5654:Vmn1r2	UTSW	4	3,172,261 (GRCm39)	missense	probably benign	0.17
R7084:Vmn1r2	UTSW	4	3,172,134 (GRCm39)	missense	probably benign	0.44
R9134:Vmn1r2	UTSW	4	3,172,884 (GRCm39)	missense	probably damaging	1.00
R9324:Vmn1r2	UTSW	4	3,172,678 (GRCm39)	missense	probably damaging	0.99
R9614:Vmn1r2	UTSW	4	3,172,587 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCCAGCATAGACAAGGGTAC -3'
(R):5'- CAACTCAGTAGGCACAGAGC -3'

Sequencing Primer
(F):5'- CACCTTTTTGCAGTGAGAGAAC -3'
(R):5'- CCCCTTGTTATTCGGGAAATATACAC -3'

Posted On

2019-11-12