Incidental Mutation 'R9343:Vmn1r119'
ID 715979
Institutional Source Beutler Lab
Gene Symbol Vmn1r119
Ensembl Gene ENSMUSG00000094010
Gene Name vomeronasal 1 receptor 119
Synonyms Gm1447, LOC384696
MMRRC Submission
Accession Numbers
Essential gene? Not available question?
Stock # R9343 (G1)
Quality Score 81.0075
Status Not validated
Chromosome 7
Chromosomal Location 20745457-20746380 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 20746358 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 8 (V8A)
Ref Sequence ENSEMBL: ENSMUSP00000127126 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164683]
AlphaFold E9Q4H3
Predicted Effect probably benign
Transcript: ENSMUST00000164683
AA Change: V8A

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000127126
Gene: ENSMUSG00000094010
AA Change: V8A

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: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 100% (45/45)
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb2 A G 2: 103,547,505 (GRCm39) I960V probably benign Het
Alpk3 A G 7: 80,742,079 (GRCm39) D632G probably benign Het
Aplp2 A T 9: 31,122,935 (GRCm39) L30Q unknown Het
Axl A T 7: 25,473,544 (GRCm39) Y361N probably damaging Het
Brinp2 A T 1: 158,077,090 (GRCm39) probably benign Het
Bsn T C 9: 107,992,701 (GRCm39) D1017G probably damaging Het
Cc2d2a A T 5: 43,875,999 (GRCm39) D1046V probably damaging Het
Cdc42bpg G A 19: 6,364,553 (GRCm39) G594S probably damaging Het
Clcn6 A G 4: 148,098,458 (GRCm39) S519P probably benign Het
Cnot2 T G 10: 116,346,326 (GRCm39) H92P Het
Col2a1 T C 15: 97,877,775 (GRCm39) D1049G probably damaging Het
Creld1 C T 6: 113,466,728 (GRCm39) A237V probably benign Het
Csf2rb2 A T 15: 78,171,287 (GRCm39) probably benign Het
Csmd3 G A 15: 48,015,001 (GRCm39) T643I probably damaging Het
Fam186b G A 15: 99,177,616 (GRCm39) A570V probably damaging Het
Fcmr A T 1: 130,802,072 (GRCm39) T109S Het
Grap C A 11: 61,562,551 (GRCm39) P174Q possibly damaging Het
Itgb5 T A 16: 33,730,826 (GRCm39) probably benign Het
Kidins220 A G 12: 25,058,078 (GRCm39) N561S probably damaging Het
Mri1 A T 8: 84,983,796 (GRCm39) S32T probably benign Het
Mrtfb T C 16: 13,218,791 (GRCm39) V479A probably benign Het
Muc4 A T 16: 32,569,971 (GRCm39) T344S possibly damaging Het
Npc1 A G 18: 12,334,769 (GRCm39) I661T possibly damaging Het
Npy1r A G 8: 67,156,751 (GRCm39) N57S probably damaging Het
Pds5b A G 5: 150,704,186 (GRCm39) D863G probably damaging Het
Phf14 T A 6: 11,961,563 (GRCm39) V400D probably damaging Het
Polr2l A G 7: 141,053,246 (GRCm39) I56T probably benign Het
Ppat A G 5: 77,063,884 (GRCm39) I422T probably benign Het
Prkcg T A 7: 3,359,124 (GRCm39) S110R possibly damaging Het
Rab7b A T 1: 131,639,540 (GRCm39) probably benign Het
Rnf152 A T 1: 105,212,251 (GRCm39) L102Q Het
Samd12 A G 15: 53,583,088 (GRCm39) V82A probably damaging Het
Serpina1e T A 12: 103,917,299 (GRCm39) R123S probably benign Het
Slit1 T A 19: 41,615,737 (GRCm39) N794I probably damaging Het
Surf6 T C 2: 26,783,006 (GRCm39) K154R probably damaging Het
Tln2 C T 9: 67,230,353 (GRCm39) A71T probably benign Het
Trim3 A G 7: 105,260,673 (GRCm39) Y649H probably benign Het
Ttll7 T A 3: 146,667,497 (GRCm39) W808R probably damaging Het
Tvp23a T C 16: 10,245,287 (GRCm39) D104G probably damaging Het
Upp2 A G 2: 58,645,339 (GRCm39) probably benign Het
Vipr1 G A 9: 121,471,993 (GRCm39) probably null Het
Vmn1r209 T A 13: 22,990,546 (GRCm39) H48L probably damaging Het
Wdr11 T C 7: 129,232,523 (GRCm39) probably null Het
Zcchc17 T C 4: 130,210,546 (GRCm39) D207G probably damaging Het
Zfp78 T C 7: 6,381,942 (GRCm39) S331P probably damaging Het
Other mutations in Vmn1r119
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01363:Vmn1r119 APN 7 20,746,056 (GRCm39) missense probably benign 0.41
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
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
Predicted Primers PCR Primer
(F):5'- GGGAGCAAAAGCCATCATGTTG -3'
(R):5'- TTCCCTGCAATTTACCTGTAATGTG -3'

Sequencing Primer
(F):5'- GAGCAAAAGCCATCATGTTGTTTGG -3'
(R):5'- TGTGTAACTAGAATACGGTCTCAC -3'
Posted On 2022-06-15