Incidental Mutation 'R2098:V1rd19'
ID 230366
Institutional Source Beutler Lab
Gene Symbol V1rd19
Ensembl Gene ENSMUSG00000092456
Gene Name vomeronasal 1 receptor, D19
Synonyms
MMRRC Submission 040102-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R2098 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 23702536-23703453 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 23703160 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 209 (L209F)
Ref Sequence ENSEMBL: ENSMUSP00000133284 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000173571]
AlphaFold Q3KNP5
Predicted Effect probably damaging
Transcript: ENSMUST00000173571
AA Change: L209F

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000133284
Gene: ENSMUSG00000092456
AA Change: L209F

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 1e-9 PFAM
Pfam:V1R 42 295 5.9e-13 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a T C 11: 109,927,405 (GRCm39) E1316G probably damaging Het
Arhgap32 C A 9: 32,171,207 (GRCm39) T1329K probably damaging Het
Arhgef10l G C 4: 140,306,743 (GRCm39) L104V probably damaging Het
Bend3 T C 10: 43,386,500 (GRCm39) S298P probably damaging Het
Cacna1b C T 2: 24,540,558 (GRCm39) V1385M probably damaging Het
Camk2d G A 3: 126,574,091 (GRCm39) G166D probably damaging Het
Cd84 G A 1: 171,713,148 (GRCm39) C291Y probably benign Het
Cdhr2 A G 13: 54,863,457 (GRCm39) I113V probably benign Het
Cfap206 G A 4: 34,719,053 (GRCm39) Q318* probably null Het
Chd9 C T 8: 91,760,615 (GRCm39) P2120L probably benign Het
Cyth1 T A 11: 118,084,479 (GRCm39) I25F probably damaging Het
Dock2 A T 11: 34,216,279 (GRCm39) N1208K probably benign Het
Dock2 A G 11: 34,609,832 (GRCm39) S203P probably damaging Het
Ehbp1l1 G T 19: 5,758,686 (GRCm39) T1652K possibly damaging Het
Eps8l2 G A 7: 140,935,705 (GRCm39) probably null Het
Fam3d T C 14: 8,361,479 (GRCm38) I47V probably benign Het
Gm10250 A G 15: 5,150,296 (GRCm39) probably benign Het
Gm9772 T C 17: 22,225,618 (GRCm39) H94R probably benign Het
Hspg2 G A 4: 137,247,420 (GRCm39) G1184D probably damaging Het
Igfn1 T A 1: 135,906,043 (GRCm39) D255V probably damaging Het
Marf1 T C 16: 13,932,064 (GRCm39) H1651R probably benign Het
Mllt10 T C 2: 18,167,464 (GRCm39) V385A possibly damaging Het
Mmp1b G A 9: 7,386,984 (GRCm39) S76L probably benign Het
Mrps2 C A 2: 28,358,327 (GRCm39) T39K probably benign Het
Myo6 T C 9: 80,188,808 (GRCm39) Y715H probably damaging Het
Nsun7 A G 5: 66,441,055 (GRCm39) E392G probably damaging Het
Obscn C T 11: 58,960,817 (GRCm39) E3374K probably damaging Het
Or2a20 G A 6: 43,194,437 (GRCm39) V197I probably benign Het
Or4c11 A T 2: 88,695,215 (GRCm39) I89F probably benign Het
Or56a4 A G 7: 104,806,478 (GRCm39) V137A probably benign Het
Or5w13 A T 2: 87,524,073 (GRCm39) M51K probably benign Het
Pkd2 C T 5: 104,626,768 (GRCm39) P317S probably damaging Het
Prl5a1 T C 13: 28,329,488 (GRCm39) S56P probably damaging Het
Psmd1 A G 1: 86,009,823 (GRCm39) probably null Het
Ptchd3 T C 11: 121,733,305 (GRCm39) C732R probably damaging Het
Rad51c A T 11: 87,293,589 (GRCm39) V71E probably benign Het
Scn11a A T 9: 119,621,560 (GRCm39) I619K possibly damaging Het
Sgpp1 T G 12: 75,763,284 (GRCm39) D299A probably damaging Het
Slc16a4 C A 3: 107,208,163 (GRCm39) Y224* probably null Het
Slc22a30 G A 19: 8,378,175 (GRCm39) S167L probably damaging Het
Slc6a5 T C 7: 49,595,315 (GRCm39) I559T probably damaging Het
Spire1 A G 18: 67,636,536 (GRCm39) F364L probably damaging Het
Srek1 G A 13: 103,881,363 (GRCm39) T421I unknown Het
St8sia4 T C 1: 95,581,253 (GRCm39) H163R probably damaging Het
Supt6 A G 11: 78,104,087 (GRCm39) probably null Het
Tas2r103 T C 6: 133,013,560 (GRCm39) T169A probably benign Het
Thrap3 A G 4: 126,073,823 (GRCm39) S308P probably damaging Het
Zfp267 T A 3: 36,220,289 (GRCm39) S771T probably benign Het
Other mutations in V1rd19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02631:V1rd19 APN 7 23,702,825 (GRCm39) missense probably damaging 1.00
IGL02898:V1rd19 APN 7 23,702,854 (GRCm39) missense probably damaging 1.00
IGL03231:V1rd19 APN 7 23,703,328 (GRCm39) missense probably benign 0.00
R0021:V1rd19 UTSW 7 23,703,029 (GRCm39) missense probably damaging 0.98
R0184:V1rd19 UTSW 7 23,702,632 (GRCm39) missense probably benign 0.06
R0391:V1rd19 UTSW 7 23,703,010 (GRCm39) missense probably damaging 0.98
R1520:V1rd19 UTSW 7 23,702,623 (GRCm39) missense probably damaging 0.99
R1635:V1rd19 UTSW 7 23,702,812 (GRCm39) missense probably benign 0.30
R1861:V1rd19 UTSW 7 23,703,149 (GRCm39) missense probably damaging 1.00
R1889:V1rd19 UTSW 7 23,702,632 (GRCm39) missense probably benign 0.06
R2008:V1rd19 UTSW 7 23,702,726 (GRCm39) nonsense probably null
R2059:V1rd19 UTSW 7 23,703,259 (GRCm39) missense probably benign 0.01
R3001:V1rd19 UTSW 7 23,703,310 (GRCm39) missense probably benign 0.00
R3002:V1rd19 UTSW 7 23,703,310 (GRCm39) missense probably benign 0.00
R4271:V1rd19 UTSW 7 23,702,839 (GRCm39) missense probably benign 0.36
R5130:V1rd19 UTSW 7 23,702,537 (GRCm39) start codon destroyed probably null 1.00
R5169:V1rd19 UTSW 7 23,703,209 (GRCm39) missense possibly damaging 0.75
R5297:V1rd19 UTSW 7 23,702,714 (GRCm39) missense probably damaging 0.99
R5924:V1rd19 UTSW 7 23,703,374 (GRCm39) missense probably benign
R6181:V1rd19 UTSW 7 23,702,640 (GRCm39) missense possibly damaging 0.46
R6540:V1rd19 UTSW 7 23,703,056 (GRCm39) nonsense probably null
R7331:V1rd19 UTSW 7 23,703,308 (GRCm39) missense probably damaging 0.97
R7332:V1rd19 UTSW 7 23,702,743 (GRCm39) missense probably benign 0.09
R8338:V1rd19 UTSW 7 23,702,674 (GRCm39) nonsense probably null
R8398:V1rd19 UTSW 7 23,703,374 (GRCm39) nonsense probably null
R8881:V1rd19 UTSW 7 23,703,081 (GRCm39) missense possibly damaging 0.95
R9536:V1rd19 UTSW 7 23,703,253 (GRCm39) missense probably damaging 1.00
X0065:V1rd19 UTSW 7 23,702,761 (GRCm39) missense probably benign 0.08
Predicted Primers PCR Primer
(F):5'- CAGAGCAAGTGTCACAAACATG -3'
(R):5'- ATGCCTCAGGGAATGATGAG -3'

Sequencing Primer
(F):5'- GTGTCACAAACATGGCAAGTTATTC -3'
(R):5'- TGTGACTACCAGCATCAG -3'
Posted On 2014-09-18