Incidental Mutation 'R5216:Vmn1r67'
ID 403478
Institutional Source Beutler Lab
Gene Symbol Vmn1r67
Ensembl Gene ENSMUSG00000046716
Gene Name vomeronasal 1 receptor 67
Synonyms V1re10
MMRRC Submission 042789-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R5216 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 10443331-10449202 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 10447163 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 57 (D57G)
Ref Sequence ENSEMBL: ENSMUSP00000154237 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055964] [ENSMUST00000226237]
AlphaFold G5E8C1
Predicted Effect probably benign
Transcript: ENSMUST00000055964
AA Change: D118G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000060746
Gene: ENSMUSG00000046716
AA Change: D118G

DomainStartEndE-ValueType
Pfam:V1R 34 292 4.3e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226237
AA Change: D57G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700097O09Rik A T 12: 55,061,162 (GRCm38) V84D probably damaging Het
Abcb1b T C 5: 8,813,705 (GRCm38) V220A probably benign Het
Actg1 A T 11: 120,347,754 (GRCm38) M82K probably damaging Het
Ahi1 T C 10: 20,960,076 (GRCm38) S103P probably benign Het
Aldh1b1 G T 4: 45,803,652 (GRCm38) G397C probably damaging Het
Arhgef3 A G 14: 27,401,842 (GRCm38) T507A probably benign Het
Atg7 A G 6: 114,724,949 (GRCm38) D682G probably damaging Het
Atp13a3 A G 16: 30,340,284 (GRCm38) I783T probably damaging Het
Atp9a T C 2: 168,674,888 (GRCm38) I362V probably benign Het
BC067074 G A 13: 113,342,413 (GRCm38) C1497Y probably benign Het
Birc6 T A 17: 74,613,470 (GRCm38) I168K probably damaging Het
Brca2 T A 5: 150,542,980 (GRCm38) Y2070N probably damaging Het
Cabp7 A G 11: 4,738,873 (GRCm38) I199T probably damaging Het
Cacng5 A G 11: 107,877,489 (GRCm38) F231L possibly damaging Het
Cngb3 T A 4: 19,415,729 (GRCm38) V413D possibly damaging Het
Col24a1 G A 3: 145,315,310 (GRCm38) E481K possibly damaging Het
Ctr9 T A 7: 111,045,458 (GRCm38) I560N possibly damaging Het
Dip2b C T 15: 100,211,986 (GRCm38) R1451C probably damaging Het
Fat3 T C 9: 16,377,537 (GRCm38) D230G probably damaging Het
Gramd4 G A 15: 86,134,785 (GRCm38) probably null Het
Grb14 C T 2: 64,917,309 (GRCm38) V369I probably benign Het
Hoxd1 A T 2: 74,764,351 (GRCm38) N317Y probably damaging Het
Kcnc4 A G 3: 107,439,441 (GRCm38) S623P probably benign Het
Klhl20 A G 1: 161,093,679 (GRCm38) probably null Het
Lamc1 C A 1: 153,227,696 (GRCm38) V1375L probably damaging Het
Lpin2 C T 17: 71,242,760 (GRCm38) S640L probably damaging Het
Ltbp4 AATTCAGGCCAAGGCTGGGATTCAGGCCGAGGCCGGGATTCAGGCCTAGGCTGGGATTCAGGC AATTCAGGCCTAGGCTGGGATTCAGGC 7: 27,327,311 (GRCm38) probably benign Het
Mgll T A 6: 88,766,329 (GRCm38) C110* probably null Het
Mmp14 A G 14: 54,437,663 (GRCm38) N251D possibly damaging Het
Olfr393 A T 11: 73,847,436 (GRCm38) S230T probably damaging Het
Olfr552 A G 7: 102,604,821 (GRCm38) T156A probably benign Het
Olfr857 T A 9: 19,713,289 (GRCm38) V154E probably benign Het
Pfkl T G 10: 78,009,670 (GRCm38) D5A probably damaging Het
Pik3c3 A G 18: 30,272,976 (GRCm38) Y9C probably damaging Het
Pkhd1l1 T A 15: 44,495,647 (GRCm38) Y417* probably null Het
Rptor G A 11: 119,843,713 (GRCm38) G514D probably damaging Het
Sulf1 T A 1: 12,796,874 (GRCm38) M94K probably benign Het
Synrg A G 11: 83,982,196 (GRCm38) T157A probably damaging Het
Syt1 T C 10: 108,642,257 (GRCm38) N102S probably benign Het
Tnip2 C T 5: 34,503,805 (GRCm38) R101H probably damaging Het
Trmt2a A G 16: 18,252,184 (GRCm38) D421G probably benign Het
Wnt2b A G 3: 104,961,345 (GRCm38) L43P possibly damaging Het
Zfp113 C T 5: 138,150,715 (GRCm38) D56N probably damaging Het
Zfp184 C T 13: 21,950,236 (GRCm38) L69F probably damaging Het
Zyx T C 6: 42,356,532 (GRCm38) V464A probably damaging Het
Other mutations in Vmn1r67
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01690:Vmn1r67 APN 7 10,446,840 (GRCm38) missense possibly damaging 0.96
IGL02812:Vmn1r67 APN 7 10,447,018 (GRCm38) missense probably benign 0.01
IGL03121:Vmn1r67 APN 7 10,447,467 (GRCm38) missense probably benign 0.00
IGL03208:Vmn1r67 APN 7 10,447,098 (GRCm38) missense possibly damaging 0.94
PIT4142001:Vmn1r67 UTSW 7 10,446,950 (GRCm38) missense probably benign 0.13
R0048:Vmn1r67 UTSW 7 10,446,866 (GRCm38) missense probably damaging 1.00
R0549:Vmn1r67 UTSW 7 10,447,714 (GRCm38) missense probably damaging 1.00
R1595:Vmn1r67 UTSW 7 10,447,670 (GRCm38) missense probably benign 0.18
R1608:Vmn1r67 UTSW 7 10,446,980 (GRCm38) missense possibly damaging 0.82
R2284:Vmn1r67 UTSW 7 10,447,673 (GRCm38) missense probably damaging 0.97
R3614:Vmn1r67 UTSW 7 10,447,429 (GRCm38) missense probably damaging 0.98
R4399:Vmn1r67 UTSW 7 10,447,549 (GRCm38) missense possibly damaging 0.89
R4542:Vmn1r67 UTSW 7 10,447,430 (GRCm38) missense probably damaging 0.99
R5655:Vmn1r67 UTSW 7 10,447,388 (GRCm38) missense probably benign 0.43
R5837:Vmn1r67 UTSW 7 10,447,022 (GRCm38) missense probably benign 0.26
R6526:Vmn1r67 UTSW 7 10,447,671 (GRCm38) missense probably benign 0.05
R6735:Vmn1r67 UTSW 7 10,447,211 (GRCm38) missense probably damaging 1.00
R6846:Vmn1r67 UTSW 7 10,446,913 (GRCm38) missense probably benign 0.04
R7086:Vmn1r67 UTSW 7 10,447,117 (GRCm38) missense possibly damaging 0.93
R7227:Vmn1r67 UTSW 7 10,447,548 (GRCm38) nonsense probably null
R7594:Vmn1r67 UTSW 7 10,447,415 (GRCm38) missense possibly damaging 0.95
R7608:Vmn1r67 UTSW 7 10,447,363 (GRCm38) missense possibly damaging 0.89
R7797:Vmn1r67 UTSW 7 10,446,976 (GRCm38) missense probably benign 0.30
R8681:Vmn1r67 UTSW 7 10,447,201 (GRCm38) missense probably benign 0.30
Predicted Primers PCR Primer
(F):5'- TCTCATGCACCTAATGGCATCC -3'
(R):5'- AGTGAGGCATTGATGTCATCACC -3'

Sequencing Primer
(F):5'- GATAGTTCTCTTTACAGGAATGCCTC -3'
(R):5'- GATGTCATCACCCCCTCTAATTGAAC -3'
Posted On 2016-07-22