Incidental Mutation 'R8233:Vmn1r119'
ID 637224
Institutional Source Beutler Lab
Gene Symbol Vmn1r119
Ensembl Gene ENSMUSG00000094010
Gene Name vomeronasal 1 receptor 119
Synonyms Gm1447, LOC384696
MMRRC Submission 067665-MU
Accession Numbers
Essential gene? Not available question?
Stock # R8233 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 20745457-20746380 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 20745932 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 150 (V150A)
Ref Sequence ENSEMBL: ENSMUSP00000127126 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164683]
AlphaFold E9Q4H3
Predicted Effect probably damaging
Transcript: ENSMUST00000164683
AA Change: V150A

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000127126
Gene: ENSMUSG00000094010
AA Change: V150A

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: 99.9%
  • 10x: 99.5%
  • 20x: 98.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503L19Rik A T 18: 70,602,687 (GRCm39) V42E probably benign Het
Abca12 T C 1: 71,390,916 (GRCm39) E153G probably benign Het
Adamts20 A C 15: 94,189,533 (GRCm39) I1440S probably benign Het
Aspm T A 1: 139,385,042 (GRCm39) S229T probably benign Het
Atp2b2 A T 6: 113,742,680 (GRCm39) probably null Het
Cd101 G T 3: 100,900,989 (GRCm39) H1032N unknown Het
Col6a2 A G 10: 76,444,540 (GRCm39) probably null Het
Crot A T 5: 9,026,027 (GRCm39) I320K possibly damaging Het
D5Ertd579e A T 5: 36,772,588 (GRCm39) D602E probably damaging Het
Degs1 A G 1: 182,107,160 (GRCm39) V69A probably benign Het
Dgkz A G 2: 91,769,994 (GRCm39) S557P probably damaging Het
Fat1 T A 8: 45,405,055 (GRCm39) L602Q Het
Gli2 A T 1: 118,772,167 (GRCm39) Y513N probably damaging Het
H2-Q10 A G 17: 35,781,983 (GRCm39) T202A probably benign Het
Hnrnpa3 A G 2: 75,492,860 (GRCm39) N195D probably benign Het
Ifna1 C T 4: 88,768,628 (GRCm39) T102I possibly damaging Het
Igfbp3 T A 11: 7,160,152 (GRCm39) H167L probably benign Het
Igfn1 T C 1: 135,895,782 (GRCm39) T1595A probably benign Het
Krt14 A G 11: 100,094,178 (GRCm39) V472A probably damaging Het
Lrrc74b T A 16: 17,376,089 (GRCm39) H187L probably benign Het
Magoh T G 4: 107,738,132 (GRCm39) V44G possibly damaging Het
Mbnl1 A T 3: 60,532,551 (GRCm39) I274L probably benign Het
Or13a27 T G 7: 139,925,411 (GRCm39) M164L probably benign Het
Or4c108 C T 2: 88,804,082 (GRCm39) R51H probably benign Het
Pdcd1 A G 1: 93,967,142 (GRCm39) V252A probably damaging Het
Peg10 C CTCA 6: 4,756,453 (GRCm39) probably benign Het
Plcxd3 A G 15: 4,546,317 (GRCm39) D107G possibly damaging Het
Polr2m T A 9: 71,390,866 (GRCm39) D112V probably benign Het
Ptprn A T 1: 75,229,796 (GRCm39) M701K probably damaging Het
Rxrb A G 17: 34,255,879 (GRCm39) D421G possibly damaging Het
Slfn4 A G 11: 83,078,355 (GRCm39) E381G probably damaging Het
Son AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG 16: 91,457,222 (GRCm39) probably benign Het
Srgap1 A G 10: 121,661,341 (GRCm39) I530T probably damaging Het
Stmn4 A G 14: 66,595,341 (GRCm39) H122R probably damaging Het
Sycp2 T C 2: 177,998,427 (GRCm39) E1031G probably damaging Het
Tle1 T C 4: 72,043,181 (GRCm39) T553A probably benign Het
Tnik T A 3: 28,609,086 (GRCm39) W217R unknown Het
Tyrp1 T C 4: 80,769,190 (GRCm39) V161A unknown Het
Usp29 T A 7: 6,965,406 (GRCm39) F416L probably benign Het
Usp45 T C 4: 21,781,736 (GRCm39) V34A probably benign 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
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
R9343:Vmn1r119 UTSW 7 20,746,358 (GRCm39) missense probably benign 0.03
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'- AGTGAGGATGTGCTGCATTC -3'
(R):5'- AATCCTTCAGTCACCTGGTGG -3'

Sequencing Primer
(F):5'- CGCTGGCGATGTCTATGAAG -3'
(R):5'- TTCAGTCACCTGGTGGCAAGAAG -3'
Posted On 2020-07-13