Incidental Mutation 'R7633:Vmn1r159'
ID 589755
Institutional Source Beutler Lab
Gene Symbol Vmn1r159
Ensembl Gene ENSMUSG00000095931
Gene Name vomeronasal 1 receptor 159
Synonyms Gm16507
MMRRC Submission 045721-MU
Accession Numbers
Essential gene? Not available question?
Stock # R7633 (G1)
Quality Score 208.009
Status Not validated
Chromosome 7
Chromosomal Location 22842688-22843605 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 22843023 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 195 (T195S)
Ref Sequence ENSEMBL: ENSMUSP00000129692 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167871]
AlphaFold K7N701
Predicted Effect probably damaging
Transcript: ENSMUST00000167871
AA Change: T195S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000129692
Gene: ENSMUSG00000095931
AA Change: T195S

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: 99.0%
Validation Efficiency 100% (52/52)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930504O13Rik C A 11: 58,447,478 M29I probably benign Het
A530084C06Rik G T 13: 31,558,995 R92S unknown Het
Acaca A G 11: 84,372,639 I2029V probably benign Het
Anks1b A C 10: 90,948,584 D1138A probably damaging Het
Atr T A 9: 95,947,118 V2508E probably damaging Het
C4b C T 17: 34,729,399 probably null Het
C530008M17Rik A G 5: 76,857,520 E576G unknown Het
Cd46 A T 1: 195,083,619 M146K probably null Het
Chp1 A G 2: 119,560,745 I28V probably benign Het
Chrnb1 T A 11: 69,792,873 R216W probably damaging Het
Clmn G A 12: 104,782,112 T392M probably benign Het
Dcxr A C 11: 120,726,453 L88R probably benign Het
Dedd C T 1: 171,338,910 P138L probably benign Het
Degs1 A G 1: 182,279,698 S35P probably damaging Het
Ehmt1 T C 2: 24,815,780 D851G possibly damaging Het
Fam117b A G 1: 59,981,534 D521G probably damaging Het
Fam26d G A 10: 34,043,908 T121M possibly damaging Het
Gm14085 A T 2: 122,486,680 R7S probably null Het
Gm21731 G A 13: 120,240,840 W57* probably null Het
Gm6882 A G 7: 21,427,652 V97A probably damaging Het
Hgs A T 11: 120,474,302 Q172L probably damaging Het
Hormad2 T C 11: 4,346,662 Q274R probably benign Het
Igkv8-19 C T 6: 70,341,399 probably benign Het
Ikbkb T C 8: 22,671,741 N377S probably benign Het
Intu G A 3: 40,654,253 G232S probably damaging Het
Mov10 A G 3: 104,797,065 S806P possibly damaging Het
Mrgprb1 A G 7: 48,447,583 F194L probably benign Het
Notch3 A T 17: 32,158,622 I160K probably benign Het
Nup155 C G 15: 8,109,453 S3W probably damaging Het
Olfr1287 A G 2: 111,449,622 I161V probably benign Het
Olfr284 A G 15: 98,340,086 I301T probably damaging Het
Plxdc1 A T 11: 97,956,151 F147L possibly damaging Het
Ppfia1 T C 7: 144,552,436 D33G possibly damaging Het
Prdm11 G A 2: 92,980,654 A200V probably damaging Het
Qrich2 A T 11: 116,456,629 I1123K unknown Het
Rgs1 A G 1: 144,248,477 probably null Het
Skint7 T A 4: 111,984,140 V259E probably benign Het
Slc25a3 A T 10: 91,118,042 probably null Het
Slco1a6 A T 6: 142,145,755 I73N probably damaging Het
Sltm C G 9: 70,586,673 P802R possibly damaging Het
Smc4 CTA CTATA 3: 69,018,067 probably benign Het
Spock2 G A 10: 60,126,180 D206N probably damaging Het
Stard3nl T G 13: 19,367,838 R185S probably damaging Het
Supt16 A G 14: 52,197,099 Y18H probably benign Het
Synpo G A 18: 60,603,428 T482I probably damaging Het
Tmc6 G T 11: 117,769,220 T694K probably benign Het
Trim59 T A 3: 69,037,926 H27L probably damaging Het
Trpv2 G A 11: 62,591,006 probably null Het
Tyw5 A T 1: 57,393,485 D117E probably benign Het
Usp17la T C 7: 104,861,147 Y320H probably damaging Het
Usp31 T C 7: 121,658,962 D694G probably damaging Het
Vmn2r57 C T 7: 41,425,089 V517M possibly damaging Het
Yipf1 A G 4: 107,318,996 N29S probably benign Het
Zfp954 A T 7: 7,115,824 F240L possibly damaging Het
Other mutations in Vmn1r159
AlleleSourceChrCoordTypePredicted EffectPPH Score
ANU23:Vmn1r159 UTSW 7 22,843,163 (GRCm38) missense probably damaging 0.99
R1183:Vmn1r159 UTSW 7 22,843,594 (GRCm38) missense probably null 0.80
R1522:Vmn1r159 UTSW 7 22,843,268 (GRCm38) missense probably damaging 0.98
R1700:Vmn1r159 UTSW 7 22,842,965 (GRCm38) missense probably damaging 1.00
R2570:Vmn1r159 UTSW 7 22,842,882 (GRCm38) missense probably benign 0.07
R3620:Vmn1r159 UTSW 7 22,842,833 (GRCm38) missense possibly damaging 0.89
R4939:Vmn1r159 UTSW 7 22,842,891 (GRCm38) missense probably damaging 1.00
R4985:Vmn1r159 UTSW 7 22,843,534 (GRCm38) missense probably damaging 1.00
R6161:Vmn1r159 UTSW 7 22,843,187 (GRCm38) missense possibly damaging 0.63
R6365:Vmn1r159 UTSW 7 22,843,401 (GRCm38) missense probably damaging 1.00
R7033:Vmn1r159 UTSW 7 22,842,864 (GRCm38) missense probably damaging 1.00
R7817:Vmn1r159 UTSW 7 22,843,062 (GRCm38) missense possibly damaging 0.47
R7846:Vmn1r159 UTSW 7 22,843,271 (GRCm38) missense probably benign 0.01
R8008:Vmn1r159 UTSW 7 22,843,240 (GRCm38) missense possibly damaging 0.56
R8019:Vmn1r159 UTSW 7 22,842,823 (GRCm38) missense probably benign 0.01
R8222:Vmn1r159 UTSW 7 22,843,183 (GRCm38) nonsense probably null
R8291:Vmn1r159 UTSW 7 22,842,830 (GRCm38) missense possibly damaging 0.94
R8817:Vmn1r159 UTSW 7 22,843,134 (GRCm38) missense probably benign 0.04
R9170:Vmn1r159 UTSW 7 22,843,340 (GRCm38) missense probably damaging 1.00
R9242:Vmn1r159 UTSW 7 22,843,487 (GRCm38) missense probably benign 0.00
R9467:Vmn1r159 UTSW 7 22,842,716 (GRCm38) missense possibly damaging 0.90
R9525:Vmn1r159 UTSW 7 22,842,992 (GRCm38) missense probably damaging 0.96
R9601:Vmn1r159 UTSW 7 22,843,191 (GRCm38) missense probably damaging 1.00
R9699:Vmn1r159 UTSW 7 22,843,250 (GRCm38) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- ACCTCACTGACAAGCCTTATGAAG -3'
(R):5'- CAGAGCAAGTGTCCCAAATTTG -3'

Sequencing Primer
(F):5'- CACTGACAAGCCTTATGAAGAAATG -3'
(R):5'- AATTTGGTGAGTTATTCTTGTTACGG -3'
Posted On 2019-10-24