Incidental Mutation 'R6920:Vmn2r71'
ID 539576
Institutional Source Beutler Lab
Gene Symbol Vmn2r71
Ensembl Gene ENSMUSG00000091205
Gene Name vomeronasal 2, receptor 71
Synonyms EG233445
MMRRC Submission 045040-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R6920 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 85264670-85273755 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 85273108 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 641 (I641F)
Ref Sequence ENSEMBL: ENSMUSP00000132337 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172338]
AlphaFold L7N2D8
Predicted Effect probably damaging
Transcript: ENSMUST00000172338
AA Change: I641F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000132337
Gene: ENSMUSG00000091205
AA Change: I641F

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 468 2.1e-31 PFAM
Pfam:NCD3G 511 563 8.7e-20 PFAM
Pfam:7tm_3 593 831 2e-55 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.1%
  • 20x: 97.2%
Validation Efficiency 100% (65/65)
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A T 3: 137,773,811 (GRCm39) Y1000F probably damaging Het
1700018B08Rik A G 8: 122,262,160 (GRCm39) probably null Het
Aadat T C 8: 60,982,467 (GRCm39) F245L probably damaging Het
Adcy10 T G 1: 165,403,227 (GRCm39) L1575W probably damaging Het
Anks4b A T 7: 119,782,231 (GRCm39) T421S probably damaging Het
Anpep A T 7: 79,475,097 (GRCm39) I155N probably damaging Het
Arnt T C 3: 95,397,932 (GRCm39) F572L probably damaging Het
Brip1 G A 11: 86,039,362 (GRCm39) Q391* probably null Het
Brpf3 C A 17: 29,042,970 (GRCm39) H1004N probably benign Het
Cand2 T A 6: 115,768,250 (GRCm39) V465D possibly damaging Het
Card10 G T 15: 78,686,609 (GRCm39) Y69* probably null Het
Catsperd A T 17: 56,962,175 (GRCm39) K450* probably null Het
Ccdc137 T C 11: 120,351,009 (GRCm39) L137P probably damaging Het
Cic T C 7: 24,990,107 (GRCm39) S1905P probably damaging Het
Csmd3 C T 15: 47,507,601 (GRCm39) G2971S probably damaging Het
Dmxl2 A G 9: 54,379,496 (GRCm39) Y183H probably damaging Het
Drosha T C 15: 12,834,396 (GRCm39) Y167H unknown Het
E330034G19Rik A G 14: 24,358,310 (GRCm39) K214R unknown Het
Fam180a T G 6: 35,290,765 (GRCm39) I73L possibly damaging Het
Fbxo28 G T 1: 182,168,986 (GRCm39) H51N probably benign Het
Gm12728 T G 4: 105,647,533 (GRCm39) probably null Het
Gm973 T C 1: 59,591,620 (GRCm39) C335R possibly damaging Het
Gpx8 A G 13: 113,179,770 (GRCm39) V177A probably damaging Het
Hdlbp A G 1: 93,340,083 (GRCm39) probably null Het
Htt T G 5: 35,034,444 (GRCm39) Y1972D probably null Het
Igkv6-14 T C 6: 70,412,116 (GRCm39) Y56C possibly damaging Het
Kcnma1 A G 14: 23,576,602 (GRCm39) probably null Het
Klc1 T C 12: 111,754,019 (GRCm39) S105P probably damaging Het
Klhl20 T C 1: 160,921,266 (GRCm39) D63G possibly damaging Het
Lamc3 A G 2: 31,798,701 (GRCm39) D469G probably damaging Het
Lrit1 G C 14: 36,782,052 (GRCm39) V242L probably damaging Het
Mboat4 G A 8: 34,591,865 (GRCm39) R434H probably benign Het
Mttp T C 3: 137,821,043 (GRCm39) K270E possibly damaging Het
Muc5ac G A 7: 141,347,035 (GRCm39) C337Y possibly damaging Het
Nars1 A G 18: 64,634,471 (GRCm39) V484A probably damaging Het
Noxa1 G T 2: 24,981,844 (GRCm39) probably null Het
Or14c45 A G 7: 86,176,522 (GRCm39) T186A probably benign Het
Or7g18 T A 9: 18,786,821 (GRCm39) L63H probably damaging Het
Osbpl7 G A 11: 96,941,584 (GRCm39) G36S probably damaging Het
P4htm C T 9: 108,460,812 (GRCm39) G220D probably benign Het
Pcdhga7 A G 18: 37,848,199 (GRCm39) I69V probably benign Het
Pla2g4e C T 2: 120,015,795 (GRCm39) E250K possibly damaging Het
Plcd4 A G 1: 74,604,994 (GRCm39) probably benign Het
Ppfia3 C A 7: 45,008,231 (GRCm39) G213V possibly damaging Het
Ppp1r1a A G 15: 103,441,513 (GRCm39) S67P probably damaging Het
Prss43 T C 9: 110,657,680 (GRCm39) F193S probably benign Het
Rfx1 A G 8: 84,822,117 (GRCm39) Y872C probably damaging Het
Rhot1 T A 11: 80,132,921 (GRCm39) N218K probably benign Het
Sall1 A G 8: 89,757,021 (GRCm39) F1028L probably damaging Het
Siglec1 G A 2: 130,919,997 (GRCm39) Q845* probably null Het
Slc38a9 C T 13: 112,838,060 (GRCm39) T275I possibly damaging Het
Slc39a4 A T 15: 76,497,470 (GRCm39) S481T probably damaging Het
Ssr1 A T 13: 38,169,998 (GRCm39) N191K probably damaging Het
Tenm4 A T 7: 96,544,757 (GRCm39) S2258C probably damaging Het
Tm7sf3 T G 6: 146,507,645 (GRCm39) R472S possibly damaging Het
Tmprss11a G A 5: 86,576,494 (GRCm39) T119M probably benign Het
Traip C T 9: 107,838,240 (GRCm39) R142* probably null Het
Utrn T C 10: 12,626,214 (GRCm39) N100D probably damaging Het
Vmn1r74 T C 7: 11,581,575 (GRCm39) S292P probably benign Het
Vmn2r9 T A 5: 108,996,912 (GRCm39) Y119F possibly damaging Het
Vmn2r98 A G 17: 19,285,510 (GRCm39) N110S probably damaging Het
Vwce A G 19: 10,642,057 (GRCm39) T928A probably benign Het
Zfp608 T A 18: 55,121,337 (GRCm39) K83N probably damaging Het
Zfp808 A G 13: 62,320,982 (GRCm39) H737R probably benign Het
Zswim4 T C 8: 84,940,714 (GRCm39) N795S probably benign Het
Other mutations in Vmn2r71
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00922:Vmn2r71 APN 7 85,267,901 (GRCm39) missense probably benign
IGL00960:Vmn2r71 APN 7 85,273,582 (GRCm39) missense probably damaging 1.00
IGL01372:Vmn2r71 APN 7 85,270,022 (GRCm39) splice site probably benign
IGL01690:Vmn2r71 APN 7 85,264,782 (GRCm39) missense probably damaging 1.00
IGL01909:Vmn2r71 APN 7 85,270,001 (GRCm39) missense probably benign 0.00
IGL01950:Vmn2r71 APN 7 85,264,827 (GRCm39) missense probably damaging 0.98
IGL02570:Vmn2r71 APN 7 85,264,748 (GRCm39) missense possibly damaging 0.95
IGL02650:Vmn2r71 APN 7 85,273,535 (GRCm39) missense probably damaging 1.00
IGL02901:Vmn2r71 APN 7 85,268,470 (GRCm39) missense probably benign 0.00
IGL03128:Vmn2r71 APN 7 85,268,795 (GRCm39) missense probably damaging 1.00
IGL03328:Vmn2r71 APN 7 85,273,499 (GRCm39) missense probably damaging 1.00
R0533:Vmn2r71 UTSW 7 85,268,426 (GRCm39) frame shift probably null
R0707:Vmn2r71 UTSW 7 85,268,640 (GRCm39) missense probably benign
R0841:Vmn2r71 UTSW 7 85,267,749 (GRCm39) missense possibly damaging 0.62
R0865:Vmn2r71 UTSW 7 85,268,516 (GRCm39) missense probably benign 0.01
R0883:Vmn2r71 UTSW 7 85,272,842 (GRCm39) missense probably benign 0.19
R0939:Vmn2r71 UTSW 7 85,272,889 (GRCm39) missense possibly damaging 0.70
R1597:Vmn2r71 UTSW 7 85,273,352 (GRCm39) missense possibly damaging 0.46
R1646:Vmn2r71 UTSW 7 85,270,476 (GRCm39) missense probably damaging 0.99
R1719:Vmn2r71 UTSW 7 85,270,435 (GRCm39) missense probably damaging 1.00
R1860:Vmn2r71 UTSW 7 85,264,782 (GRCm39) missense probably damaging 1.00
R2013:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2014:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2015:Vmn2r71 UTSW 7 85,269,845 (GRCm39) missense probably benign 0.38
R2050:Vmn2r71 UTSW 7 85,273,681 (GRCm39) missense probably damaging 1.00
R2084:Vmn2r71 UTSW 7 85,267,945 (GRCm39) missense probably benign 0.03
R2221:Vmn2r71 UTSW 7 85,273,301 (GRCm39) missense probably benign 0.40
R2223:Vmn2r71 UTSW 7 85,273,301 (GRCm39) missense probably benign 0.40
R2245:Vmn2r71 UTSW 7 85,273,388 (GRCm39) missense probably damaging 1.00
R3115:Vmn2r71 UTSW 7 85,272,866 (GRCm39) missense probably damaging 0.97
R3122:Vmn2r71 UTSW 7 85,264,828 (GRCm39) nonsense probably null
R3609:Vmn2r71 UTSW 7 85,268,870 (GRCm39) missense probably damaging 1.00
R4093:Vmn2r71 UTSW 7 85,270,442 (GRCm39) missense probably benign 0.00
R4305:Vmn2r71 UTSW 7 85,273,360 (GRCm39) missense probably damaging 1.00
R4306:Vmn2r71 UTSW 7 85,273,360 (GRCm39) missense probably damaging 1.00
R4334:Vmn2r71 UTSW 7 85,269,042 (GRCm39) missense probably benign 0.01
R4569:Vmn2r71 UTSW 7 85,273,402 (GRCm39) missense possibly damaging 0.66
R4622:Vmn2r71 UTSW 7 85,269,817 (GRCm39) missense probably benign 0.00
R4915:Vmn2r71 UTSW 7 85,270,476 (GRCm39) missense probably damaging 0.99
R4956:Vmn2r71 UTSW 7 85,268,436 (GRCm39) missense probably benign 0.19
R5005:Vmn2r71 UTSW 7 85,273,352 (GRCm39) missense probably damaging 1.00
R5045:Vmn2r71 UTSW 7 85,273,597 (GRCm39) missense probably benign 0.00
R5153:Vmn2r71 UTSW 7 85,268,430 (GRCm39) missense possibly damaging 0.94
R5236:Vmn2r71 UTSW 7 85,272,877 (GRCm39) missense probably damaging 1.00
R5373:Vmn2r71 UTSW 7 85,267,750 (GRCm39) missense possibly damaging 0.79
R5405:Vmn2r71 UTSW 7 85,268,622 (GRCm39) missense probably benign
R5831:Vmn2r71 UTSW 7 85,272,922 (GRCm39) missense probably benign 0.16
R6061:Vmn2r71 UTSW 7 85,268,482 (GRCm39) missense probably benign
R6518:Vmn2r71 UTSW 7 85,270,436 (GRCm39) missense probably damaging 1.00
R6751:Vmn2r71 UTSW 7 85,269,095 (GRCm39) critical splice donor site probably null
R7358:Vmn2r71 UTSW 7 85,273,468 (GRCm39) missense possibly damaging 0.81
R7453:Vmn2r71 UTSW 7 85,273,297 (GRCm39) missense probably benign 0.21
R7560:Vmn2r71 UTSW 7 85,273,115 (GRCm39) missense probably benign 0.06
R7871:Vmn2r71 UTSW 7 85,272,869 (GRCm39) missense possibly damaging 0.81
R8267:Vmn2r71 UTSW 7 85,264,704 (GRCm39) missense probably benign 0.02
R8377:Vmn2r71 UTSW 7 85,264,707 (GRCm39) missense probably benign
R9278:Vmn2r71 UTSW 7 85,269,788 (GRCm39) missense probably benign 0.19
R9319:Vmn2r71 UTSW 7 85,273,694 (GRCm39) missense probably damaging 1.00
R9329:Vmn2r71 UTSW 7 85,267,950 (GRCm39) missense probably benign 0.00
R9368:Vmn2r71 UTSW 7 85,273,442 (GRCm39) missense probably damaging 1.00
R9636:Vmn2r71 UTSW 7 85,268,388 (GRCm39) missense possibly damaging 0.80
R9756:Vmn2r71 UTSW 7 85,268,573 (GRCm39) nonsense probably null
X0025:Vmn2r71 UTSW 7 85,267,873 (GRCm39) missense probably benign
Z1186:Vmn2r71 UTSW 7 85,273,094 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AATGAAGACCATACTCTCTGTCTC -3'
(R):5'- TTTGGGTGCTCCTGACTCAG -3'

Sequencing Primer
(F):5'- CTCTGTCTCCAAAAAGTTGTGG -3'
(R):5'- TGACTCAGGCATCCACCTC -3'
Posted On 2018-11-06