Incidental Mutation 'IGL01431:Vmn1r79'
ID 84105
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r79
Ensembl Gene ENSMUSG00000096735
Gene Name vomeronasal 1 receptor 79
Synonyms Gm9807
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # IGL01431
Quality Score
Status
Chromosome 7
Chromosomal Location 11910120-11911040 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 11910327 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 70 (S70P)
Ref Sequence ENSEMBL: ENSMUSP00000154092 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062811] [ENSMUST00000210112] [ENSMUST00000226953] [ENSMUST00000227530]
AlphaFold Q8R285
Predicted Effect possibly damaging
Transcript: ENSMUST00000062811
AA Change: S70P

PolyPhen 2 Score 0.876 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000056232
Gene: ENSMUSG00000096735
AA Change: S70P

DomainStartEndE-ValueType
Pfam:TAS2R 7 302 4.9e-9 PFAM
Pfam:7tm_1 27 292 2.8e-7 PFAM
Pfam:V1R 34 298 1.7e-35 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210112
Predicted Effect possibly damaging
Transcript: ENSMUST00000226953
AA Change: S70P

PolyPhen 2 Score 0.876 (Sensitivity: 0.83; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227530
AA Change: S70P

PolyPhen 2 Score 0.876 (Sensitivity: 0.83; Specificity: 0.93)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts7 A G 9: 90,089,838 (GRCm39) I897T possibly damaging Het
Aqp2 G A 15: 99,477,301 (GRCm39) V90M possibly damaging Het
Atf6 T C 1: 170,680,571 (GRCm39) probably benign Het
Cdh3 T C 8: 107,274,301 (GRCm39) Y607H probably damaging Het
Cer1 T A 4: 82,801,068 (GRCm39) E198D probably benign Het
Dscam A G 16: 96,453,278 (GRCm39) probably null Het
Ecel1 C T 1: 87,079,226 (GRCm39) R484H probably damaging Het
Entpd7 C A 19: 43,718,278 (GRCm39) H575Q probably benign Het
F11r T C 1: 171,290,477 (GRCm39) V279A probably damaging Het
Gm17093 T A 14: 44,759,122 (GRCm39) probably benign Het
Got1 T A 19: 43,491,488 (GRCm39) K321* probably null Het
Gpn1 T C 5: 31,664,882 (GRCm39) V302A probably benign Het
Hivep1 G T 13: 42,311,493 (GRCm39) K1244N probably damaging Het
Idh3b T C 2: 130,123,817 (GRCm39) T116A possibly damaging Het
Itgb4 C A 11: 115,897,283 (GRCm39) probably benign Het
Mybl1 G T 1: 9,742,872 (GRCm39) L579I probably damaging Het
Myh14 T A 7: 44,263,782 (GRCm39) T1694S probably null Het
Mylk3 T C 8: 86,063,030 (GRCm39) D537G probably damaging Het
Myo1d A C 11: 80,565,665 (GRCm39) F387V probably damaging Het
Nek9 T C 12: 85,361,361 (GRCm39) Y448C probably benign Het
Or8k40 A T 2: 86,584,508 (GRCm39) H191Q probably benign Het
Paxbp1 T C 16: 90,832,804 (GRCm39) probably benign Het
Potefam1 A T 2: 111,055,740 (GRCm39) probably benign Het
Retreg2 T A 1: 75,121,749 (GRCm39) probably null Het
Ripply3 G A 16: 94,129,402 (GRCm39) C16Y possibly damaging Het
Robo3 G A 9: 37,330,407 (GRCm39) probably benign Het
Rrm1 C A 7: 102,106,759 (GRCm39) probably benign Het
Rsad2 T A 12: 26,498,666 (GRCm39) R269S probably benign Het
Sbp A T 17: 24,164,322 (GRCm39) probably benign Het
Schip1 A T 3: 68,525,110 (GRCm39) Q162L probably damaging Het
Senp1 T C 15: 97,980,144 (GRCm39) Y67C probably damaging Het
Slc25a25 C T 2: 32,309,103 (GRCm39) R233K probably damaging Het
Smoc1 C A 12: 81,199,525 (GRCm39) S220* probably null Het
Stab1 C A 14: 30,870,952 (GRCm39) R1299I probably benign Het
Stk17b A G 1: 53,805,074 (GRCm39) probably benign Het
Tmc7 T G 7: 118,151,985 (GRCm39) D312A probably damaging Het
Zfc3h1 C A 10: 115,259,128 (GRCm39) T1591K possibly damaging Het
Other mutations in Vmn1r79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00592:Vmn1r79 APN 7 11,910,934 (GRCm39) missense probably benign 0.05
IGL01953:Vmn1r79 APN 7 11,910,382 (GRCm39) missense probably damaging 1.00
PIT4418001:Vmn1r79 UTSW 7 11,910,766 (GRCm39) missense probably damaging 1.00
R0831:Vmn1r79 UTSW 7 11,910,990 (GRCm39) missense probably damaging 0.98
R1791:Vmn1r79 UTSW 7 11,910,358 (GRCm39) missense probably damaging 1.00
R1869:Vmn1r79 UTSW 7 11,910,574 (GRCm39) missense probably benign 0.00
R3713:Vmn1r79 UTSW 7 11,910,139 (GRCm39) missense possibly damaging 0.66
R4210:Vmn1r79 UTSW 7 11,910,415 (GRCm39) missense possibly damaging 0.46
R4243:Vmn1r79 UTSW 7 11,910,971 (GRCm39) nonsense probably null
R4244:Vmn1r79 UTSW 7 11,910,971 (GRCm39) nonsense probably null
R4839:Vmn1r79 UTSW 7 11,910,361 (GRCm39) missense probably benign 0.30
R5677:Vmn1r79 UTSW 7 11,910,928 (GRCm39) missense possibly damaging 0.77
R6048:Vmn1r79 UTSW 7 11,910,448 (GRCm39) missense probably damaging 0.99
R7388:Vmn1r79 UTSW 7 11,910,668 (GRCm39) nonsense probably null
R7751:Vmn1r79 UTSW 7 11,910,762 (GRCm39) nonsense probably null
R8207:Vmn1r79 UTSW 7 11,910,415 (GRCm39) missense possibly damaging 0.46
R9462:Vmn1r79 UTSW 7 11,910,261 (GRCm39) missense probably damaging 1.00
R9664:Vmn1r79 UTSW 7 11,910,582 (GRCm39) missense probably benign 0.00
R9749:Vmn1r79 UTSW 7 11,910,450 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-11