Incidental Mutation 'R5834:Vmn1r238'
ID 449511
Institutional Source Beutler Lab
Gene Symbol Vmn1r238
Ensembl Gene ENSMUSG00000091539
Gene Name vomeronasal 1 receptor, 238
Synonyms
MMRRC Submission 044055-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # R5834 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 3122492-3123412 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 3123168 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 82 (E82G)
Ref Sequence ENSEMBL: ENSMUSP00000129804 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165255]
AlphaFold E9Q373
Predicted Effect probably benign
Transcript: ENSMUST00000165255
AA Change: E82G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000129804
Gene: ENSMUSG00000091539
AA Change: E82G

DomainStartEndE-ValueType
Pfam:TAS2R 7 302 5.3e-8 PFAM
Pfam:7tm_1 27 292 8.8e-7 PFAM
Pfam:V1R 34 298 1.9e-33 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.8%
  • 20x: 96.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931428F04Rik G A 8: 105,282,123 (GRCm38) Q421* probably null Het
Abca13 T C 11: 9,277,974 (GRCm38) probably null Het
Adamts20 A C 15: 94,353,584 (GRCm38) S441A probably damaging Het
Aen T A 7: 78,907,301 (GRCm38) M299K probably damaging Het
Akap3 T C 6: 126,865,833 (GRCm38) S472P probably benign Het
Ank3 T G 10: 69,822,257 (GRCm38) V158G probably damaging Het
Arfgap1 A G 2: 180,981,162 (GRCm38) D324G probably benign Het
Aste1 A T 9: 105,403,415 (GRCm38) R448S probably benign Het
Atp10a T A 7: 58,658,618 (GRCm38) L55Q probably benign Het
C1qtnf9 G A 14: 60,779,450 (GRCm38) G143D probably damaging Het
Camsap2 A G 1: 136,280,388 (GRCm38) V1122A probably benign Het
Cbl T C 9: 44,233,779 (GRCm38) H37R probably damaging Het
Cfap61 A C 2: 146,129,149 (GRCm38) D893A probably benign Het
Chd2 T A 7: 73,478,715 (GRCm38) I841F probably damaging Het
Chd9 A G 8: 90,997,164 (GRCm38) T622A probably damaging Het
Cntnap3 A G 13: 64,748,577 (GRCm38) Y1028H probably benign Het
Crybg2 A G 4: 134,074,123 (GRCm38) T865A probably benign Het
Cyp2c55 A G 19: 39,042,067 (GRCm38) I448V probably benign Het
Cyth1 T A 11: 118,192,463 (GRCm38) probably null Het
Dcaf13 C T 15: 39,143,642 (GRCm38) R324* probably null Het
Dhx37 C A 5: 125,425,730 (GRCm38) R42L probably damaging Het
Dock1 T A 7: 134,763,933 (GRCm38) V450E probably damaging Het
Ednrb A G 14: 103,820,877 (GRCm38) L330P probably damaging Het
Eml4 T A 17: 83,477,741 (GRCm38) H778Q probably damaging Het
Evx1 T A 6: 52,315,990 (GRCm38) I227N probably damaging Het
G3bp1 T A 11: 55,497,940 (GRCm38) V326E probably benign Het
Gata2 T C 6: 88,200,747 (GRCm38) V253A probably benign Het
Gbp2 A G 3: 142,633,377 (GRCm38) N397D probably damaging Het
Gm14401 C A 2: 177,086,903 (GRCm38) H261N probably benign Het
Hacd4 A T 4: 88,398,152 (GRCm38) H243Q probably benign Het
Hsd3b1 C A 3: 98,852,939 (GRCm38) K245N possibly damaging Het
Hyls1 G A 9: 35,561,184 (GRCm38) S312F probably benign Het
Ift27 A T 15: 78,165,243 (GRCm38) C86S probably damaging Het
Iqgap2 C T 13: 95,675,372 (GRCm38) R707H probably damaging Het
Irs3 T A 5: 137,644,559 (GRCm38) S206C probably damaging Het
Lefty2 C T 1: 180,893,151 (GRCm38) probably benign Het
Mark3 A G 12: 111,624,487 (GRCm38) I162V probably damaging Het
Mefv A C 16: 3,716,046 (GRCm38) D120E probably damaging Het
Mep1a G A 17: 43,478,164 (GRCm38) H574Y probably benign Het
Mre11a A G 9: 14,799,657 (GRCm38) I45V probably benign Het
Mtor A G 4: 148,536,536 (GRCm38) N1797S possibly damaging Het
Nav1 A C 1: 135,532,406 (GRCm38) M393R probably benign Het
Nod2 T C 8: 88,664,639 (GRCm38) S510P possibly damaging Het
Nos2 C T 11: 78,928,579 (GRCm38) T39I probably benign Het
Olfr474 T A 7: 107,954,906 (GRCm38) H88Q probably benign Het
Olfr93 A T 17: 37,151,799 (GRCm38) Y58N probably damaging Het
Pcdh7 A G 5: 57,721,628 (GRCm38) S842G possibly damaging Het
Pcdha11 T C 18: 37,012,623 (GRCm38) V589A probably damaging Het
Plaa A C 4: 94,583,469 (GRCm38) V10G probably damaging Het
Pprc1 T A 19: 46,065,220 (GRCm38) probably benign Het
Ptprt T C 2: 161,560,269 (GRCm38) Y994C probably damaging Het
Ripply2 T A 9: 87,015,890 (GRCm38) W37R probably damaging Het
Rpgrip1 A G 14: 52,158,382 (GRCm38) D1227G probably damaging Het
Scoc C T 8: 83,437,631 (GRCm38) D10N possibly damaging Het
Sdk2 A T 11: 113,854,273 (GRCm38) I732N probably damaging Het
Six2 T C 17: 85,687,664 (GRCm38) K97E probably damaging Het
Slit2 A C 5: 48,259,647 (GRCm38) N1014H probably damaging Het
Smc1b A C 15: 85,089,665 (GRCm38) L930R probably damaging Het
Spag16 T A 1: 69,923,714 (GRCm38) M340K probably benign Het
Spata31 C T 13: 64,922,666 (GRCm38) S876L probably benign Het
Spen A G 4: 141,471,843 (GRCm38) Y3135H possibly damaging Het
Spta1 A T 1: 174,184,797 (GRCm38) probably null Het
Stk3 G A 15: 34,959,018 (GRCm38) T336I probably damaging Het
Tas2r118 T A 6: 23,969,877 (GRCm38) T62S probably benign Het
Tmprss11d A G 5: 86,306,310 (GRCm38) M212T probably damaging Het
Trpc7 A G 13: 56,776,158 (GRCm38) L738P probably damaging Het
Ttll8 A G 15: 88,917,246 (GRCm38) V413A possibly damaging Het
Usb1 G A 8: 95,333,533 (GRCm38) probably benign Het
Vmn2r114 T C 17: 23,310,625 (GRCm38) T168A possibly damaging Het
Vmn2r60 C A 7: 42,116,508 (GRCm38) P13H probably benign Het
Wdr26 A G 1: 181,203,147 (GRCm38) L194P probably damaging Het
Zfhx2 G A 14: 55,073,330 (GRCm38) Q636* probably null Het
Zfyve26 A G 12: 79,266,537 (GRCm38) Y25H probably benign Het
Other mutations in Vmn1r238
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00427:Vmn1r238 APN 18 3,123,243 (GRCm38) missense probably benign 0.01
IGL01385:Vmn1r238 APN 18 3,122,770 (GRCm38) missense possibly damaging 0.83
IGL02716:Vmn1r238 APN 18 3,123,124 (GRCm38) missense probably damaging 1.00
R1219:Vmn1r238 UTSW 18 3,123,135 (GRCm38) missense possibly damaging 0.81
R1568:Vmn1r238 UTSW 18 3,123,358 (GRCm38) missense probably benign 0.00
R1864:Vmn1r238 UTSW 18 3,123,040 (GRCm38) nonsense probably null
R3024:Vmn1r238 UTSW 18 3,123,305 (GRCm38) missense probably benign 0.13
R4291:Vmn1r238 UTSW 18 3,123,214 (GRCm38) nonsense probably null
R4304:Vmn1r238 UTSW 18 3,123,040 (GRCm38) nonsense probably null
R4586:Vmn1r238 UTSW 18 3,123,294 (GRCm38) missense probably damaging 1.00
R4664:Vmn1r238 UTSW 18 3,123,300 (GRCm38) missense probably damaging 0.99
R5123:Vmn1r238 UTSW 18 3,123,243 (GRCm38) missense probably benign
R5430:Vmn1r238 UTSW 18 3,122,521 (GRCm38) missense possibly damaging 0.63
R7186:Vmn1r238 UTSW 18 3,122,661 (GRCm38) missense probably damaging 0.99
R7206:Vmn1r238 UTSW 18 3,122,623 (GRCm38) missense possibly damaging 0.94
R7308:Vmn1r238 UTSW 18 3,122,875 (GRCm38) missense probably benign 0.09
R7346:Vmn1r238 UTSW 18 3,123,151 (GRCm38) missense probably damaging 1.00
R7467:Vmn1r238 UTSW 18 3,123,393 (GRCm38) missense probably benign 0.10
R7571:Vmn1r238 UTSW 18 3,122,721 (GRCm38) missense probably damaging 1.00
R7808:Vmn1r238 UTSW 18 3,123,033 (GRCm38) missense probably benign 0.03
R8085:Vmn1r238 UTSW 18 3,123,151 (GRCm38) missense probably damaging 1.00
R8086:Vmn1r238 UTSW 18 3,123,250 (GRCm38) missense probably damaging 1.00
R8325:Vmn1r238 UTSW 18 3,122,529 (GRCm38) missense probably benign 0.00
R8423:Vmn1r238 UTSW 18 3,123,365 (GRCm38) nonsense probably null
R8747:Vmn1r238 UTSW 18 3,123,232 (GRCm38) missense possibly damaging 0.87
R8930:Vmn1r238 UTSW 18 3,123,127 (GRCm38) missense probably benign 0.03
R8932:Vmn1r238 UTSW 18 3,123,127 (GRCm38) missense probably benign 0.03
R9279:Vmn1r238 UTSW 18 3,122,994 (GRCm38) missense probably damaging 0.99
R9382:Vmn1r238 UTSW 18 3,122,676 (GRCm38) missense probably damaging 0.99
R9644:Vmn1r238 UTSW 18 3,122,635 (GRCm38) missense probably benign 0.10
R9725:Vmn1r238 UTSW 18 3,122,577 (GRCm38) missense probably benign 0.00
Z1177:Vmn1r238 UTSW 18 3,122,505 (GRCm38) missense probably benign 0.00
Predicted Primers
Posted On 2016-12-20