Incidental Mutation 'R6906:Vmn1r171'
ID 538777
Institutional Source Beutler Lab
Gene Symbol Vmn1r171
Ensembl Gene ENSMUSG00000062483
Gene Name vomeronasal 1 receptor 171
Synonyms V1rd7, V3R7
MMRRC Submission 044998-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R6906 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 23331413-23332993 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 23331804 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 10 (V10I)
Ref Sequence ENSEMBL: ENSMUSP00000077552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078458] [ENSMUST00000226128] [ENSMUST00000226321] [ENSMUST00000226733] [ENSMUST00000226771] [ENSMUST00000227386] [ENSMUST00000227774] [ENSMUST00000227866] [ENSMUST00000228228] [ENSMUST00000228484] [ENSMUST00000228559] [ENSMUST00000228674] [ENSMUST00000228681]
AlphaFold Q9EPS6
Predicted Effect probably benign
Transcript: ENSMUST00000078458
AA Change: V10I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000077552
Gene: ENSMUSG00000062483
AA Change: V10I

DomainStartEndE-ValueType
Pfam:TAS2R 20 307 1.7e-14 PFAM
Pfam:7tm_1 42 300 3.4e-7 PFAM
Pfam:V1R 53 307 1.1e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226128
Predicted Effect probably benign
Transcript: ENSMUST00000226321
Predicted Effect probably benign
Transcript: ENSMUST00000226733
Predicted Effect probably benign
Transcript: ENSMUST00000226771
Predicted Effect probably benign
Transcript: ENSMUST00000227386
Predicted Effect probably benign
Transcript: ENSMUST00000227774
Predicted Effect probably benign
Transcript: ENSMUST00000227866
Predicted Effect probably benign
Transcript: ENSMUST00000228228
Predicted Effect probably benign
Transcript: ENSMUST00000228484
Predicted Effect probably benign
Transcript: ENSMUST00000228559
Predicted Effect probably benign
Transcript: ENSMUST00000228674
Predicted Effect probably benign
Transcript: ENSMUST00000228681
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.2%
  • 20x: 97.3%
Validation Efficiency 98% (45/46)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf2 A G 5: 24,773,840 (GRCm39) F350L possibly damaging Het
Ahnak2 T A 12: 112,748,933 (GRCm39) T305S probably benign Het
Anp32a A G 9: 62,284,851 (GRCm39) probably benign Het
Aplf A G 6: 87,607,068 (GRCm39) S449P possibly damaging Het
Arl6ip4 A G 5: 124,254,614 (GRCm39) R36G possibly damaging Het
Ascc1 G A 10: 59,840,674 (GRCm39) D12N probably benign Het
Bin1 C A 18: 32,554,978 (GRCm39) H243Q probably benign Het
Ccdc168 C T 1: 44,095,173 (GRCm39) S1975N probably benign Het
Ccdc7a C A 8: 129,662,162 (GRCm39) V547L unknown Het
Cntnap5c T A 17: 58,702,302 (GRCm39) N1207K probably benign Het
Coro7 C A 16: 4,451,168 (GRCm39) R507L probably benign Het
Crtap T A 9: 114,210,700 (GRCm39) K291N probably benign Het
Csmd3 T C 15: 47,710,569 (GRCm39) T1569A probably benign Het
Dmrta1 A G 4: 89,580,203 (GRCm39) T388A probably benign Het
Ehd3 T C 17: 74,137,333 (GRCm39) F501L probably damaging Het
Fbn2 A C 18: 58,204,891 (GRCm39) L1184R possibly damaging Het
Fhip1b G A 7: 105,037,476 (GRCm39) T369I probably damaging Het
Hsf1 T C 15: 76,361,919 (GRCm39) probably null Het
Hycc1 A T 5: 24,204,956 (GRCm39) W12R probably damaging Het
Kansl1l T C 1: 66,762,437 (GRCm39) H810R possibly damaging Het
Lrp5 A T 19: 3,672,638 (GRCm39) I557N probably damaging Het
Lypd1 T C 1: 125,838,196 (GRCm39) E41G probably damaging Het
Mgam A G 6: 40,724,853 (GRCm39) Y443C probably damaging Het
Muc2 A G 7: 141,284,976 (GRCm39) D871G probably damaging Het
Nup85 T A 11: 115,471,769 (GRCm39) Y198N probably damaging Het
Obscn T A 11: 58,923,744 (GRCm39) M6578L possibly damaging Het
Or8h7 T C 2: 86,721,091 (GRCm39) T143A probably benign Het
Osbpl5 G C 7: 143,248,065 (GRCm39) Q667E probably damaging Het
Ovgp1 T A 3: 105,894,189 (GRCm39) probably benign Het
Prl8a2 T A 13: 27,532,900 (GRCm39) N37K probably benign Het
Ptprf A T 4: 118,126,474 (GRCm39) I93N possibly damaging Het
Rnf112 T C 11: 61,341,215 (GRCm39) S457G probably null Het
Sema3e A G 5: 14,290,601 (GRCm39) D562G probably damaging Het
Sesn3 A G 9: 14,236,937 (GRCm39) M472V probably damaging Het
Sfpq GCCGCCGCAGCAGCCTCCGCCGCAGCAGCC GCCGCCGCAGCAGCC 4: 126,915,419 (GRCm39) probably benign Het
Shc3 T C 13: 51,620,595 (GRCm39) T144A probably damaging Het
Sis A G 3: 72,826,818 (GRCm39) L1287P probably damaging Het
Srrm2 C T 17: 24,039,337 (GRCm39) P2090S probably damaging Het
Syne2 T G 12: 76,042,760 (GRCm39) D3910E possibly damaging Het
Tcaim C T 9: 122,663,839 (GRCm39) T443I probably benign Het
Tex19.1 T C 11: 121,037,948 (GRCm39) V102A probably benign Het
Tpd52l1 T G 10: 31,208,950 (GRCm39) T168P possibly damaging Het
Trdn G A 10: 33,109,944 (GRCm39) C294Y probably benign Het
Trmt1l T C 1: 151,327,926 (GRCm39) Y479H probably benign Het
Zbtb41 T A 1: 139,351,128 (GRCm39) D80E possibly damaging Het
Zcchc4 A G 5: 52,980,976 (GRCm39) K473E possibly damaging Het
Other mutations in Vmn1r171
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01088:Vmn1r171 APN 7 23,332,252 (GRCm39) missense probably damaging 1.00
IGL02963:Vmn1r171 APN 7 23,332,113 (GRCm39) missense possibly damaging 0.62
FR4304:Vmn1r171 UTSW 7 23,332,105 (GRCm39) missense probably benign 0.26
R0412:Vmn1r171 UTSW 7 23,332,080 (GRCm39) missense possibly damaging 0.81
R0602:Vmn1r171 UTSW 7 23,332,602 (GRCm39) missense probably benign 0.01
R0710:Vmn1r171 UTSW 7 23,332,426 (GRCm39) missense probably damaging 1.00
R1758:Vmn1r171 UTSW 7 23,331,781 (GRCm39) missense probably benign 0.25
R2007:Vmn1r171 UTSW 7 23,332,012 (GRCm39) missense probably damaging 1.00
R4153:Vmn1r171 UTSW 7 23,332,077 (GRCm39) missense probably damaging 1.00
R4799:Vmn1r171 UTSW 7 23,332,369 (GRCm39) missense probably benign 0.31
R5038:Vmn1r171 UTSW 7 23,332,188 (GRCm39) missense probably benign 0.00
R6087:Vmn1r171 UTSW 7 23,332,429 (GRCm39) missense probably damaging 1.00
R7745:Vmn1r171 UTSW 7 23,332,035 (GRCm39) missense probably benign 0.00
R8954:Vmn1r171 UTSW 7 23,332,525 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACACACAGATCTATCATGAGGAAAG -3'
(R):5'- ATCAAGGTATTGCCCACAGC -3'

Sequencing Primer
(F):5'- GATCTATCATGAGGAAAGAAAGAGC -3'
(R):5'- ATTGCCCACAGCTAAGTTGG -3'
Posted On 2018-11-06