Incidental Mutation 'R0048:Vmn1r67'
ID 64245
Institutional Source Beutler Lab
Gene Symbol Vmn1r67
Ensembl Gene ENSMUSG00000046716
Gene Name vomeronasal 1 receptor 67
Synonyms V1re10
MMRRC Submission 038342-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # R0048 (G1)
Quality Score 131
Status Validated
Chromosome 7
Chromosomal Location 10180716-10181714 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 10180793 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Glutamic Acid at position 19 (G19E)
Ref Sequence ENSEMBL: ENSMUSP00000060746 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055964] [ENSMUST00000226237]
AlphaFold G5E8C1
Predicted Effect probably damaging
Transcript: ENSMUST00000055964
AA Change: G19E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000060746
Gene: ENSMUSG00000046716
AA Change: G19E

DomainStartEndE-ValueType
Pfam:V1R 34 292 4.3e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226237
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.9%
  • 20x: 96.3%
Validation Efficiency 100% (37/37)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb3 A G 1: 25,140,563 (GRCm39) I299T probably benign Het
Ankrd12 A G 17: 66,291,798 (GRCm39) S1212P probably damaging Het
Ankrd50 A G 3: 38,537,198 (GRCm39) S52P probably benign Het
Brca1 A G 11: 101,415,803 (GRCm39) V777A possibly damaging Het
Cblif G A 19: 11,727,120 (GRCm39) V110M possibly damaging Het
Dppa2 A G 16: 48,137,761 (GRCm39) M248V probably benign Het
Fat2 G T 11: 55,200,865 (GRCm39) H736Q probably benign Het
Fgfr2 A T 7: 129,782,218 (GRCm39) probably benign Het
Hmcn2 T C 2: 31,318,249 (GRCm39) S3865P possibly damaging Het
Iqgap3 A T 3: 88,023,256 (GRCm39) T516S probably benign Het
Itpr2 T C 6: 146,133,789 (GRCm39) probably null Het
Lrrfip1 C T 1: 91,021,369 (GRCm39) probably benign Het
Mfsd12 G A 10: 81,198,648 (GRCm39) V380I possibly damaging Het
Mroh9 G A 1: 162,890,056 (GRCm39) T227M probably damaging Het
Mtor C T 4: 148,623,338 (GRCm39) Q2063* probably null Het
Nanos3 C T 8: 84,902,763 (GRCm39) R133Q probably damaging Het
Or13c3 C A 4: 52,856,196 (GRCm39) A106S probably damaging Het
Ptgfr A G 3: 151,540,728 (GRCm39) V260A possibly damaging Het
Raph1 T C 1: 60,539,764 (GRCm39) K423E probably benign Het
Rbm27 A G 18: 42,431,529 (GRCm39) D112G probably benign Het
Ryr2 T C 13: 11,610,670 (GRCm39) E4052G probably damaging Het
Sart3 G T 5: 113,893,458 (GRCm39) D346E possibly damaging Het
Siglec1 T C 2: 130,915,317 (GRCm39) T1425A possibly damaging Het
Snx25 A T 8: 46,558,146 (GRCm39) probably benign Het
Son T A 16: 91,455,865 (GRCm39) H1537Q possibly damaging Het
Tgfb1 T A 7: 25,393,779 (GRCm39) probably benign Het
Umodl1 A T 17: 31,187,451 (GRCm39) N172Y probably damaging Het
Urah C T 7: 140,416,665 (GRCm39) T46I probably damaging Het
Usp8 C T 2: 126,579,809 (GRCm39) P353L probably damaging Het
Vamp2 A G 11: 68,980,585 (GRCm39) D51G possibly damaging Het
Wdr76 C T 2: 121,365,900 (GRCm39) probably benign Het
Wwox C A 8: 115,166,570 (GRCm39) P20Q probably damaging Het
Other mutations in Vmn1r67
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01690:Vmn1r67 APN 7 10,180,767 (GRCm39) missense possibly damaging 0.96
IGL02812:Vmn1r67 APN 7 10,180,945 (GRCm39) missense probably benign 0.01
IGL03121:Vmn1r67 APN 7 10,181,394 (GRCm39) missense probably benign 0.00
IGL03208:Vmn1r67 APN 7 10,181,025 (GRCm39) missense possibly damaging 0.94
PIT4142001:Vmn1r67 UTSW 7 10,180,877 (GRCm39) missense probably benign 0.13
R0549:Vmn1r67 UTSW 7 10,181,641 (GRCm39) missense probably damaging 1.00
R1595:Vmn1r67 UTSW 7 10,181,597 (GRCm39) missense probably benign 0.18
R1608:Vmn1r67 UTSW 7 10,180,907 (GRCm39) missense possibly damaging 0.82
R2284:Vmn1r67 UTSW 7 10,181,600 (GRCm39) missense probably damaging 0.97
R3614:Vmn1r67 UTSW 7 10,181,356 (GRCm39) missense probably damaging 0.98
R4399:Vmn1r67 UTSW 7 10,181,476 (GRCm39) missense possibly damaging 0.89
R4542:Vmn1r67 UTSW 7 10,181,357 (GRCm39) missense probably damaging 0.99
R5216:Vmn1r67 UTSW 7 10,181,090 (GRCm39) missense probably benign 0.00
R5655:Vmn1r67 UTSW 7 10,181,315 (GRCm39) missense probably benign 0.43
R5837:Vmn1r67 UTSW 7 10,180,949 (GRCm39) missense probably benign 0.26
R6526:Vmn1r67 UTSW 7 10,181,598 (GRCm39) missense probably benign 0.05
R6735:Vmn1r67 UTSW 7 10,181,138 (GRCm39) missense probably damaging 1.00
R6846:Vmn1r67 UTSW 7 10,180,840 (GRCm39) missense probably benign 0.04
R7086:Vmn1r67 UTSW 7 10,181,044 (GRCm39) missense possibly damaging 0.93
R7227:Vmn1r67 UTSW 7 10,181,475 (GRCm39) nonsense probably null
R7594:Vmn1r67 UTSW 7 10,181,342 (GRCm39) missense possibly damaging 0.95
R7608:Vmn1r67 UTSW 7 10,181,290 (GRCm39) missense possibly damaging 0.89
R7797:Vmn1r67 UTSW 7 10,180,903 (GRCm39) missense probably benign 0.30
R8681:Vmn1r67 UTSW 7 10,181,128 (GRCm39) missense probably benign 0.30
Predicted Primers PCR Primer
(F):5'- ACCCCTCTGATTTAGCCTCAGTAGC -3'
(R):5'- GCACCCAATGTACTTTGCAGCATTC -3'

Sequencing Primer
(F):5'- GATTTAGCCTCAGTAGCTCTTCAG -3'
(R):5'- CCTTAAAGCAGGATTTCCTGTGAC -3'
Posted On 2013-08-06