Incidental Mutation 'R2877:Vmn1r215'
ID260635
Institutional Source Beutler Lab
Gene Symbol Vmn1r215
Ensembl Gene ENSMUSG00000099917
Gene Namevomeronasal 1 receptor 215
SynonymsV1ri2
MMRRC Submission 040465-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.093) question?
Stock #R2877 (G1)
Quality Score225
Status Validated
Chromosome13
Chromosomal Location23068025-23078006 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 23076561 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Arginine at position 257 (H257R)
Ref Sequence ENSEMBL: ENSMUSP00000154763 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072972] [ENSMUST00000228092]
Predicted Effect probably benign
Transcript: ENSMUST00000072972
AA Change: H257R

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000072739
Gene: ENSMUSG00000099917
AA Change: H257R

DomainStartEndE-ValueType
Pfam:V1R 35 298 2.4e-37 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000228092
AA Change: H257R

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 96% (66/69)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930522L14Rik A C 5: 109,738,945 probably benign Het
Abca13 C T 11: 9,291,889 L1251F possibly damaging Het
Accsl A T 2: 93,859,410 M384K probably damaging Het
Adssl1 A C 12: 112,634,189 K197N probably damaging Het
Alg11 A G 8: 22,065,358 N170D possibly damaging Het
Ambn T C 5: 88,460,700 probably benign Het
Anapc7 T C 5: 122,428,156 Y43H probably benign Het
Anxa10 T A 8: 62,060,339 I255F probably damaging Het
Atg2b A T 12: 105,664,009 Y374* probably null Het
Axl T A 7: 25,766,524 M563L probably damaging Het
Carmil2 A G 8: 105,695,423 E1108G probably damaging Het
Casp1 T C 9: 5,303,110 M188T probably damaging Het
Chd3 A T 11: 69,361,172 C87* probably null Het
Col6a3 G A 1: 90,775,599 T2475I unknown Het
Creb3l4 A T 3: 90,242,308 S83R probably damaging Het
Cyp2a4 G A 7: 26,312,187 E278K possibly damaging Het
Dync1li2 A C 8: 104,429,415 Y265D probably damaging Het
Eif3f G A 7: 108,934,812 probably null Het
Eipr1 C T 12: 28,760,092 T22I possibly damaging Het
Fbxo48 A G 11: 16,953,382 K3E possibly damaging Het
Fbxw13 A G 9: 109,181,466 F368S probably damaging Het
Fbxw19 A T 9: 109,485,970 W175R probably damaging Het
Fibcd1 G A 2: 31,838,666 P60S probably benign Het
Foxa3 A T 7: 19,014,880 M107K probably benign Het
Foxj2 G A 6: 122,842,832 D560N probably damaging Het
Gfm2 A G 13: 97,153,249 R181G possibly damaging Het
Gpr25 C T 1: 136,260,815 G20D possibly damaging Het
Grin1 A G 2: 25,297,629 V594A probably damaging Het
Itpripl1 A G 2: 127,141,614 V196A probably benign Het
Kcns1 A G 2: 164,164,762 I427T probably damaging Het
Kiz T C 2: 146,889,556 V322A possibly damaging Het
Mslnl G A 17: 25,742,934 V128M probably damaging Het
Muc19 T A 15: 91,893,006 noncoding transcript Het
Naa16 A G 14: 79,343,298 M592T probably benign Het
Nat6 A T 9: 107,583,168 E87D possibly damaging Het
Ncapd3 T A 9: 27,044,487 probably null Het
Nebl C A 2: 17,434,929 D178Y probably damaging Het
Nedd1 T A 10: 92,714,126 N99I possibly damaging Het
Nuak1 T C 10: 84,375,345 D293G possibly damaging Het
Olfr1036 T C 2: 86,075,331 M197T possibly damaging Het
Olfr1487 A T 19: 13,619,632 I157F probably damaging Het
Palb2 A G 7: 122,114,429 V877A probably damaging Het
Rassf6 C T 5: 90,606,805 V205I probably damaging Het
Rbak A G 5: 143,174,105 Y398H probably damaging Het
Rcbtb1 A G 14: 59,210,592 probably benign Het
Robo4 CGG CG 9: 37,411,490 probably null Het
Smpdl3a C A 10: 57,809,085 T317K probably damaging Het
Speer4e C T 5: 14,937,116 V92M probably damaging Het
Syne2 A G 12: 76,000,831 I4009V probably benign Het
Tarbp1 G A 8: 126,427,832 L1474F probably damaging Het
Tchh A G 3: 93,444,228 E325G unknown Het
Trpc4 T C 3: 54,291,340 S562P probably damaging Het
Ttn T C 2: 76,737,065 D27828G probably damaging Het
Ulk4 T C 9: 121,260,039 D258G probably benign Het
Vmn2r56 A C 7: 12,711,027 M433R probably benign Het
Vmn2r76 C A 7: 86,225,993 C592F probably benign Het
Zcchc8 C T 5: 123,700,703 V591I probably benign Het
Znhit6 G C 3: 145,576,654 G96A probably benign Het
Other mutations in Vmn1r215
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00923:Vmn1r215 APN 13 23076249 missense probably damaging 0.98
IGL02515:Vmn1r215 APN 13 23075820 missense probably benign 0.21
IGL03061:Vmn1r215 APN 13 23075918 missense probably damaging 0.97
PIT4651001:Vmn1r215 UTSW 13 23076360 missense probably damaging 0.97
R0196:Vmn1r215 UTSW 13 23076084 missense probably damaging 1.00
R0816:Vmn1r215 UTSW 13 23075954 missense probably benign 0.00
R0817:Vmn1r215 UTSW 13 23075954 missense probably benign 0.00
R0820:Vmn1r215 UTSW 13 23075954 missense probably benign 0.00
R1104:Vmn1r215 UTSW 13 23076588 missense possibly damaging 0.50
R1733:Vmn1r215 UTSW 13 23076678 missense probably benign 0.43
R1912:Vmn1r215 UTSW 13 23076503 missense possibly damaging 0.94
R2010:Vmn1r215 UTSW 13 23076208 missense probably damaging 1.00
R2510:Vmn1r215 UTSW 13 23076173 missense probably benign 0.00
R2511:Vmn1r215 UTSW 13 23076173 missense probably benign 0.00
R3429:Vmn1r215 UTSW 13 23076208 missense probably damaging 1.00
R3854:Vmn1r215 UTSW 13 23075888 missense probably benign
R4124:Vmn1r215 UTSW 13 23075993 missense probably benign 0.42
R4235:Vmn1r215 UTSW 13 23075931 missense probably benign 0.31
R4979:Vmn1r215 UTSW 13 23075894 missense probably benign 0.04
R4991:Vmn1r215 UTSW 13 23076527 missense probably damaging 1.00
R5011:Vmn1r215 UTSW 13 23076551 missense probably damaging 1.00
R5026:Vmn1r215 UTSW 13 23076279 missense probably benign 0.30
R5070:Vmn1r215 UTSW 13 23076496 missense probably benign 0.03
R5589:Vmn1r215 UTSW 13 23076019 missense probably damaging 1.00
R5589:Vmn1r215 UTSW 13 23076020 missense probably damaging 1.00
R5651:Vmn1r215 UTSW 13 23075811 missense possibly damaging 0.93
R5928:Vmn1r215 UTSW 13 23076317 missense possibly damaging 0.50
R6176:Vmn1r215 UTSW 13 23076358 missense probably damaging 1.00
R6228:Vmn1r215 UTSW 13 23076463 missense probably benign 0.19
R7270:Vmn1r215 UTSW 13 23075919 missense possibly damaging 0.77
R7313:Vmn1r215 UTSW 13 23076314 missense probably benign 0.01
R7820:Vmn1r215 UTSW 13 23076545 missense probably damaging 1.00
R8515:Vmn1r215 UTSW 13 23075867 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GGTCCATGGCTCTCAATCTG -3'
(R):5'- CATTAGGTCCCCACATCTACAATTC -3'

Sequencing Primer
(F):5'- GGTCCATGGCTCTCAATCTGTATAAG -3'
(R):5'- CCCACATCTACAATTCATTATGGG -3'
Posted On2015-01-23