Incidental Mutation 'R9525:Vmn1r159'
ID 719147
Institutional Source Beutler Lab
Gene Symbol Vmn1r159
Ensembl Gene ENSMUSG00000095931
Gene Name vomeronasal 1 receptor 159
Synonyms Gm16507
MMRRC Submission
Accession Numbers
Essential gene? Not available question?
Stock # R9525 (G1)
Quality Score 216.009
Status Not validated
Chromosome 7
Chromosomal Location 22542113-22543030 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22542417 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 205 (V205A)
Ref Sequence ENSEMBL: ENSMUSP00000129692 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167871]
AlphaFold K7N701
Predicted Effect probably damaging
Transcript: ENSMUST00000167871
AA Change: V205A

PolyPhen 2 Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000129692
Gene: ENSMUSG00000095931
AA Change: V205A

DomainStartEndE-ValueType
Pfam:TAS2R 8 297 1.8e-16 PFAM
Pfam:7tm_1 31 288 7e-8 PFAM
Pfam:V1R 41 296 6.3e-16 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm2 T A 4: 144,282,000 (GRCm39) D264V possibly damaging Het
Adgrv1 C T 13: 81,593,453 (GRCm39) G4178E possibly damaging Het
Alpk2 A G 18: 65,399,288 (GRCm39) Y2097H probably damaging Het
Anapc2 T C 2: 25,166,339 (GRCm39) S369P probably damaging Het
Atr C T 9: 95,792,610 (GRCm39) A1644V possibly damaging Het
Camsap1 G A 2: 25,843,962 (GRCm39) H230Y probably benign Het
Cbx7 A C 15: 79,814,797 (GRCm39) W35G probably damaging Het
Cc2d2b T C 19: 40,773,430 (GRCm39) Y498H probably damaging Het
Ccdc162 T A 10: 41,559,222 (GRCm39) R126W probably damaging Het
Cd274 T A 19: 29,359,879 (GRCm39) L228Q probably benign Het
Cfap57 A T 4: 118,433,778 (GRCm39) I1000N probably damaging Het
Cfhr4 G T 1: 139,702,250 (GRCm39) T78K probably damaging Het
Chadl C A 15: 81,578,220 (GRCm39) G470C probably damaging Het
Clasp2 T C 9: 113,740,677 (GRCm39) L1217P probably damaging Het
Crnkl1 A G 2: 145,770,198 (GRCm39) V215A probably benign Het
Dbx2 G T 15: 95,552,304 (GRCm39) H114N probably benign Het
Ddb2 T G 2: 91,065,180 (GRCm39) T82P probably benign Het
Emc8 T C 8: 121,394,656 (GRCm39) Y21C probably damaging Het
Epha1 A T 6: 42,344,758 (GRCm39) M66K probably damaging Het
Fan1 A C 7: 64,022,007 (GRCm39) probably null Het
Fgd2 T A 17: 29,583,955 (GRCm39) L123Q probably damaging Het
Flnb T A 14: 7,905,481 (GRCm38) V1077E probably damaging Het
Fnbp1l A T 3: 122,352,703 (GRCm39) M251K probably damaging Het
Gal3st2c T A 1: 93,935,928 (GRCm39) F93L probably damaging Het
Gdf2 T C 14: 33,667,564 (GRCm39) *429Q probably null Het
Gdpd5 A G 7: 99,104,156 (GRCm39) T455A possibly damaging Het
Gm8356 G T 14: 17,691,339 (GRCm39) Q109K Het
Gpr20 A T 15: 73,567,681 (GRCm39) V236E probably benign Het
Gpr39 T C 1: 125,800,323 (GRCm39) V358A probably damaging Het
Grin1 T C 2: 25,187,472 (GRCm39) N613D probably damaging Het
H2bc15 G T 13: 21,938,305 (GRCm39) A5S unknown Het
Hepacam2 A G 6: 3,476,046 (GRCm39) V293A probably benign Het
Igf1r G A 7: 67,864,682 (GRCm39) R1160Q probably damaging Het
Iqcd T C 5: 120,738,217 (GRCm39) Y12H probably benign Het
Itih1 T C 14: 30,658,711 (GRCm39) S393G probably benign Het
Klhl33 T C 14: 51,128,929 (GRCm39) M507V probably null Het
Mast4 G T 13: 102,872,944 (GRCm39) H2141Q probably benign Het
Mkrn2 T A 6: 115,587,486 (GRCm39) D54E probably damaging Het
Mrm3 A G 11: 76,141,104 (GRCm39) T371A possibly damaging Het
Msantd5f3 G A 4: 73,573,061 (GRCm39) S100N probably benign Het
Mylk2 T A 2: 152,759,552 (GRCm39) M414K probably damaging Het
Nlrp4b A G 7: 10,448,748 (GRCm39) E317G probably damaging Het
Or51b6b A T 7: 103,310,142 (GRCm39) I105N probably damaging Het
Or51i2 A G 7: 103,689,820 (GRCm39) I272M possibly damaging Het
Or8k20 A G 2: 86,106,484 (GRCm39) S116P probably benign Het
Pcdhb18 T A 18: 37,624,887 (GRCm39) V739E probably damaging Het
Pkhd1l1 A T 15: 44,448,322 (GRCm39) T3834S possibly damaging Het
Pkp3 A G 7: 140,668,310 (GRCm39) D546G probably damaging Het
Pot1a A T 6: 25,745,916 (GRCm39) M595K probably benign Het
Pus7l A G 15: 94,438,764 (GRCm39) I27T probably damaging Het
Rbp3 A G 14: 33,676,402 (GRCm39) I117V probably benign Het
Rnf19a A T 15: 36,247,375 (GRCm39) L454H probably damaging Het
Rps6kb1 C A 11: 86,410,746 (GRCm39) K167N possibly damaging Het
Saxo1 A T 4: 86,363,186 (GRCm39) Y432* probably null Het
Setdb2 A T 14: 59,646,841 (GRCm39) V558E probably benign Het
Spmap2l A G 5: 77,195,138 (GRCm39) N104S probably benign Het
Tbck T C 3: 132,456,966 (GRCm39) F627L probably damaging Het
Tbpl2 T G 2: 23,986,547 (GRCm39) M1L probably benign Het
Timp2 A C 11: 118,194,678 (GRCm39) D170E probably benign Het
Tomm40 A G 7: 19,436,812 (GRCm39) Y303H probably damaging Het
Trgv5 T C 13: 19,376,885 (GRCm39) C111R probably damaging Het
Trhr T C 15: 44,060,873 (GRCm39) I131T possibly damaging Het
Vmn2r25 G T 6: 123,800,164 (GRCm39) T726K probably damaging Het
Wwox T A 8: 115,433,105 (GRCm39) V257E probably benign Het
Xxylt1 A G 16: 30,869,593 (GRCm39) I169T probably benign Het
Zfp1007 A T 5: 109,824,846 (GRCm39) N201K Het
Zfp457 T C 13: 67,441,492 (GRCm39) Y361C probably damaging Het
Other mutations in Vmn1r159
AlleleSourceChrCoordTypePredicted EffectPPH Score
ANU23:Vmn1r159 UTSW 7 22,542,588 (GRCm39) missense probably damaging 0.99
R1183:Vmn1r159 UTSW 7 22,543,019 (GRCm39) missense probably null 0.80
R1522:Vmn1r159 UTSW 7 22,542,693 (GRCm39) missense probably damaging 0.98
R1700:Vmn1r159 UTSW 7 22,542,390 (GRCm39) missense probably damaging 1.00
R2570:Vmn1r159 UTSW 7 22,542,307 (GRCm39) missense probably benign 0.07
R3620:Vmn1r159 UTSW 7 22,542,258 (GRCm39) missense possibly damaging 0.89
R4939:Vmn1r159 UTSW 7 22,542,316 (GRCm39) missense probably damaging 1.00
R4985:Vmn1r159 UTSW 7 22,542,959 (GRCm39) missense probably damaging 1.00
R6161:Vmn1r159 UTSW 7 22,542,612 (GRCm39) missense possibly damaging 0.63
R6365:Vmn1r159 UTSW 7 22,542,826 (GRCm39) missense probably damaging 1.00
R7033:Vmn1r159 UTSW 7 22,542,289 (GRCm39) missense probably damaging 1.00
R7633:Vmn1r159 UTSW 7 22,542,448 (GRCm39) missense probably damaging 1.00
R7817:Vmn1r159 UTSW 7 22,542,487 (GRCm39) missense possibly damaging 0.47
R7846:Vmn1r159 UTSW 7 22,542,696 (GRCm39) missense probably benign 0.01
R8008:Vmn1r159 UTSW 7 22,542,665 (GRCm39) missense possibly damaging 0.56
R8019:Vmn1r159 UTSW 7 22,542,248 (GRCm39) missense probably benign 0.01
R8222:Vmn1r159 UTSW 7 22,542,608 (GRCm39) nonsense probably null
R8291:Vmn1r159 UTSW 7 22,542,255 (GRCm39) missense possibly damaging 0.94
R8817:Vmn1r159 UTSW 7 22,542,559 (GRCm39) missense probably benign 0.04
R9170:Vmn1r159 UTSW 7 22,542,765 (GRCm39) missense probably damaging 1.00
R9242:Vmn1r159 UTSW 7 22,542,912 (GRCm39) missense probably benign 0.00
R9467:Vmn1r159 UTSW 7 22,542,141 (GRCm39) missense possibly damaging 0.90
R9601:Vmn1r159 UTSW 7 22,542,616 (GRCm39) missense probably damaging 1.00
R9699:Vmn1r159 UTSW 7 22,542,675 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- ACCTCACTGACAAGCCTTATG -3'
(R):5'- TCAGAGCAAGTGTCCCAAATTTG -3'

Sequencing Primer
(F):5'- CACTGACAAGCCTTATGAAGAAATG -3'
(R):5'- GTTGGTTTTTCAGTGTCTTAAGTAAC -3'
Posted On 2022-07-18