Incidental Mutation 'R6160:Vmn1r119'
ID489805
Institutional Source Beutler Lab
Gene Symbol Vmn1r119
Ensembl Gene ENSMUSG00000094010
Gene Namevomeronasal 1 receptor 119
SynonymsLOC384696, Gm1447
MMRRC Submission 044307-MU
Accession Numbers
Is this an essential gene? Not available question?
Stock #R6160 (G1)
Quality Score225.009
Status Not validated
Chromosome7
Chromosomal Location21011532-21012455 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 21011815 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Proline at position 214 (H214P)
Ref Sequence ENSEMBL: ENSMUSP00000127126 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164683]
Predicted Effect possibly damaging
Transcript: ENSMUST00000164683
AA Change: H214P

PolyPhen 2 Score 0.470 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000127126
Gene: ENSMUSG00000094010
AA Change: H214P

DomainStartEndE-ValueType
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
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.8%
Validation Efficiency 94% (62/66)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810474O19Rik G A 6: 149,331,507 probably null Het
4930433I11Rik T A 7: 40,993,526 S297R possibly damaging Het
5530400C23Rik A G 6: 133,294,326 E111G possibly damaging Het
8030423J24Rik T A 13: 70,883,910 S34T unknown Het
Ace3 T A 11: 105,994,732 W20R possibly damaging Het
Adgrf1 A G 17: 43,310,687 E605G probably damaging Het
Arhgap44 G A 11: 65,162,549 probably benign Het
Atm A C 9: 53,490,959 H1404Q probably benign Het
AW209491 A G 13: 14,636,721 E53G probably damaging Het
Cdt1 C T 8: 122,571,368 T366I probably benign Het
Cerk A T 15: 86,142,773 C179S probably benign Het
Cldn10 T C 14: 118,861,843 V123A possibly damaging Het
Clip1 T C 5: 123,613,541 K726E possibly damaging Het
Dcaf12 A T 4: 41,294,043 Y365N probably damaging Het
Dennd6b A G 15: 89,188,821 L171P probably damaging Het
Dip2c G A 13: 9,533,254 V91I probably benign Het
Dlec1 A G 9: 119,143,319 I1431V probably benign Het
Egln1 T C 8: 124,948,492 D188G probably damaging Het
Enpp5 T A 17: 44,081,368 N229K possibly damaging Het
Fmo1 T G 1: 162,836,298 I221L probably benign Het
Fsip2 G A 2: 82,987,945 W4674* probably null Het
Gm12185 G A 11: 48,908,428 Q413* probably null Het
Gm5096 G A 18: 87,757,121 C256Y probably damaging Het
Gm7298 A T 6: 121,764,927 H436L probably benign Het
Gucy2c G A 6: 136,740,686 Q430* probably null Het
Hgd A G 16: 37,613,298 H134R probably damaging Het
Hoxd8 A G 2: 74,705,999 E151G probably damaging Het
Il15ra A G 2: 11,720,016 D99G probably damaging Het
Ints4 T A 7: 97,509,583 probably null Het
Itgb1 T A 8: 128,720,283 F426L possibly damaging Het
Itpr1 A C 6: 108,518,755 I2534L probably benign Het
Kcnq4 T A 4: 120,716,559 H235L probably damaging Het
Kcnt1 T A 2: 25,892,383 I178N probably damaging Het
Kidins220 A G 12: 24,997,311 D252G probably damaging Het
Krt23 A G 11: 99,485,718 I204T probably damaging Het
Lipo4 A G 19: 33,503,293 L225P probably damaging Het
Lrp3 T C 7: 35,204,123 D245G possibly damaging Het
Mmp16 A G 4: 18,051,857 D282G probably damaging Het
Myo1c A T 11: 75,650,742 H18L probably benign Het
Myo1f C A 17: 33,604,344 P981Q probably benign Het
Nle1 A T 11: 82,908,157 F33I probably benign Het
Nlrp4e T G 7: 23,321,306 M406R probably damaging Het
Obscn A T 11: 59,051,785 V4857E probably damaging Het
Palb2 A T 7: 122,128,420 probably null Het
Phospho1 A T 11: 95,830,624 E22V probably damaging Het
Pom121l2 C T 13: 21,983,668 S703L possibly damaging Het
Prex2 T C 1: 10,993,851 L20P probably damaging Het
Psmb7 T C 2: 38,643,381 T45A probably damaging Het
R3hdm2 T C 10: 127,484,507 I532T probably damaging Het
Rcn1 T C 2: 105,392,017 D208G probably damaging Het
Recql5 A G 11: 115,932,787 probably null Het
Rfc4 A T 16: 23,114,683 I242N probably damaging Het
Rims1 T C 1: 22,432,984 Y650C probably damaging Het
Shc2 C T 10: 79,627,019 probably null Het
Slc14a2 A T 18: 78,158,975 probably null Het
Slc6a6 A T 6: 91,740,014 probably null Het
Synj2 C A 17: 6,008,061 H275N possibly damaging Het
T A T 17: 8,441,786 T410S probably benign Het
Tarsl2 A G 7: 65,682,779 I543V probably benign Het
Tbc1d8 T A 1: 39,372,403 K1117N probably damaging Het
Tm7sf3 A T 6: 146,606,289 L425* probably null Het
Trav14-3 A G 14: 53,763,521 Y63C probably damaging Het
Tyro3 A C 2: 119,803,270 D133A probably damaging Het
Vmn2r120 G A 17: 57,509,418 P646S probably benign Het
Zbtb7c A T 18: 76,145,833 Y454F probably benign Het
Zmym2 T C 14: 56,950,309 L1144P probably damaging Het
Other mutations in Vmn1r119
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01363:Vmn1r119 APN 7 21012131 missense probably benign 0.41
IGL02218:Vmn1r119 APN 7 21011636 missense probably benign 0.11
R0639:Vmn1r119 UTSW 7 21011668 missense possibly damaging 0.70
R1844:Vmn1r119 UTSW 7 21012196 missense probably damaging 1.00
R2250:Vmn1r119 UTSW 7 21012259 missense probably damaging 1.00
R2927:Vmn1r119 UTSW 7 21012131 missense probably benign 0.41
R4279:Vmn1r119 UTSW 7 21011861 missense probably benign 0.00
R5022:Vmn1r119 UTSW 7 21012320 missense probably benign 0.08
R6523:Vmn1r119 UTSW 7 21011852 missense possibly damaging 0.75
R7013:Vmn1r119 UTSW 7 21011789 missense probably damaging 1.00
R7218:Vmn1r119 UTSW 7 21011647 missense probably benign 0.00
R7320:Vmn1r119 UTSW 7 21012346 missense probably damaging 0.99
X0060:Vmn1r119 UTSW 7 21012283 missense possibly damaging 0.79
Predicted Primers PCR Primer
(F):5'- CTCACTGACAAGCCTTACGAAG -3'
(R):5'- GCAAGTGTCACAAACATGGC -3'

Sequencing Primer
(F):5'- CTGACAAGCCTTACGAAGAAATG -3'
(R):5'- GTGTCACAAACATGGCAAGTTATTC -3'
Posted On2017-10-10