Incidental Mutation 'R1693:Vmn1r113'
ID191927
Institutional Source Beutler Lab
Gene Symbol Vmn1r113
Ensembl Gene ENSMUSG00000091638
Gene Namevomeronasal 1 receptor 113
SynonymsGm5748
MMRRC Submission 039726-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.062) question?
Stock #R1693 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location20787285-20788208 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 20787607 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Tyrosine at position 108 (C108Y)
Ref Sequence ENSEMBL: ENSMUSP00000133307 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168794] [ENSMUST00000173723]
Predicted Effect probably damaging
Transcript: ENSMUST00000168794
AA Change: C108Y

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000126041
Gene: ENSMUSG00000091638
AA Change: C108Y

DomainStartEndE-ValueType
Pfam:TAS2R 8 288 4.2e-8 PFAM
Pfam:V1R 41 288 2.8e-8 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000173723
AA Change: C108Y

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000133307
Gene: ENSMUSG00000091638
AA Change: C108Y

DomainStartEndE-ValueType
Pfam:TAS2R 8 298 4e-16 PFAM
Pfam:7tm_1 31 290 9.3e-7 PFAM
Pfam:V1R 41 298 5e-17 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.2%
  • 20x: 92.2%
Validation Efficiency 96% (69/72)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aff4 A G 11: 53,396,553 D378G probably damaging Het
Anpep C T 7: 79,838,256 E518K probably benign Het
Aox1 T C 1: 58,085,542 Y981H probably damaging Het
Arfgap2 T A 2: 91,270,075 probably null Het
Ccnf TGGGGG TGGGGGGG 17: 24,226,540 probably null Het
Cd53 T C 3: 106,768,889 N54S possibly damaging Het
Cep152 C A 2: 125,566,254 A1390S probably benign Het
Chd7 T C 4: 8,864,307 probably null Het
Chrm5 A G 2: 112,479,280 L497P probably damaging Het
Colec12 G A 18: 9,866,765 V659M unknown Het
Creb3 C A 4: 43,566,755 H390Q probably damaging Het
D1Pas1 T C 1: 186,968,029 F52L probably benign Het
D5Ertd579e A G 5: 36,614,097 F985L probably damaging Het
Dock4 C T 12: 40,834,722 P1742S probably benign Het
Ehmt2 G T 17: 34,906,410 V534L possibly damaging Het
Epcam A G 17: 87,639,896 D26G probably benign Het
F2 C T 2: 91,629,179 V420M probably damaging Het
Fbxw16 A T 9: 109,436,259 D401E possibly damaging Het
Fiz1 T C 7: 5,008,728 T264A probably benign Het
Fsbp T C 4: 11,583,745 V148A probably benign Het
Furin A G 7: 80,392,482 L455P probably damaging Het
Ggt7 G A 2: 155,506,475 R10W probably damaging Het
Gucy2g T C 19: 55,222,926 E624G probably damaging Het
Igf2r A G 17: 12,704,316 F1202S probably damaging Het
Ikzf1 C T 11: 11,707,838 P32S probably damaging Het
Itgal G A 7: 127,305,281 V309M probably damaging Het
Kcnk5 C A 14: 20,141,896 R399L probably damaging Het
Kdm5b C T 1: 134,597,576 probably benign Het
Lrp2 C T 2: 69,510,418 V1038M probably damaging Het
Lrp4 T C 2: 91,492,353 Y1096H probably damaging Het
Lrrc7 C G 3: 158,084,533 S1465T possibly damaging Het
Maats1 A G 16: 38,341,723 Y19H probably benign Het
Map3k5 A G 10: 20,104,242 N832S probably damaging Het
Mkl2 C A 16: 13,398,470 L349I possibly damaging Het
Mkl2 T A 16: 13,398,471 L349Q probably damaging Het
Myh13 A C 11: 67,341,484 M495L possibly damaging Het
Myh9 A C 15: 77,812,897 Y106D probably damaging Het
Naa16 A T 14: 79,351,456 W452R probably damaging Het
Nsd1 T C 13: 55,247,261 S892P probably benign Het
Nup205 A G 6: 35,210,971 I939V probably benign Het
Oit3 A G 10: 59,425,417 F476S probably damaging Het
Olfr868 T C 9: 20,101,587 V276A probably benign Het
Panx3 A T 9: 37,668,907 M50K possibly damaging Het
Panx3 A C 9: 37,668,946 M37R possibly damaging Het
Ppp2r5e C G 12: 75,469,567 A239P probably damaging Het
Prkaca T A 8: 83,981,198 D37E probably benign Het
Prkcq T A 2: 11,254,199 I310N probably damaging Het
Prrc2c A G 1: 162,718,713 Y235H probably damaging Het
Ptprj A T 2: 90,449,797 C1052* probably null Het
Rad52 C A 6: 119,916,035 P180Q probably damaging Het
Sdhaf3 T A 6: 7,038,964 D95E probably benign Het
Slitrk6 A G 14: 110,750,928 I449T probably damaging Het
Spata7 T A 12: 98,664,257 M358K possibly damaging Het
Tada2a C T 11: 84,082,069 G178D probably damaging Het
Tap2 G C 17: 34,209,212 V287L probably benign Het
Tmem200a A G 10: 25,993,979 F131L possibly damaging Het
Tmem55a T A 4: 14,886,631 D68E probably benign Het
Traip A T 9: 107,970,030 K356M probably damaging Het
Tspan8 T A 10: 115,844,044 probably benign Het
U2surp A T 9: 95,511,860 M1K probably null Het
Vars A T 17: 34,998,196 D427E probably benign Het
Vmn2r63 T A 7: 42,928,319 Q265L probably benign Het
Vps33b T A 7: 80,287,893 V463E probably damaging Het
Vrtn T C 12: 84,648,655 S60P probably benign Het
Zfp53 T A 17: 21,509,622 V639D possibly damaging Het
Zfp964 T A 8: 69,664,150 S466T possibly damaging Het
Other mutations in Vmn1r113
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01908:Vmn1r113 APN 7 20788018 missense probably damaging 1.00
IGL02082:Vmn1r113 APN 7 20787747 missense probably benign
IGL02148:Vmn1r113 APN 7 20787822 missense probably benign 0.14
IGL03169:Vmn1r113 APN 7 20788087 missense probably benign 0.11
R0593:Vmn1r113 UTSW 7 20787463 missense probably damaging 0.99
R0669:Vmn1r113 UTSW 7 20787420 missense probably benign 0.00
R1212:Vmn1r113 UTSW 7 20787431 missense probably benign 0.19
R2228:Vmn1r113 UTSW 7 20787907 missense probably damaging 1.00
R3945:Vmn1r113 UTSW 7 20787712 missense probably benign 0.00
R4209:Vmn1r113 UTSW 7 20787610 missense probably benign 0.44
R5038:Vmn1r113 UTSW 7 20787494 missense possibly damaging 0.70
R6306:Vmn1r113 UTSW 7 20787867 missense probably damaging 1.00
R6623:Vmn1r113 UTSW 7 20788066 missense probably benign 0.01
R6675:Vmn1r113 UTSW 7 20787978 missense probably benign 0.02
R6677:Vmn1r113 UTSW 7 20787978 missense probably benign 0.02
R6678:Vmn1r113 UTSW 7 20787978 missense probably benign 0.02
R6968:Vmn1r113 UTSW 7 20787951 missense probably damaging 1.00
R7054:Vmn1r113 UTSW 7 20787502 missense probably benign 0.14
R7256:Vmn1r113 UTSW 7 20787445 missense probably damaging 1.00
R8926:Vmn1r113 UTSW 7 20787949 missense possibly damaging 0.82
Predicted Primers PCR Primer
(F):5'- GGAAAAGCCCTCTCCATGTCTGTTC -3'
(R):5'- ACACTGGTCCAGACCATGATGCTC -3'

Sequencing Primer
(F):5'- TTGACTGGTTCTAAACAGAGACCC -3'
(R):5'- CAGACCATGATGCTCATGAATGTG -3'
Posted On2014-05-14