Incidental Mutation 'R9159:Vmn2r73'
ID 695577
Institutional Source Beutler Lab
Gene Symbol Vmn2r73
Ensembl Gene ENSMUSG00000070458
Gene Name vomeronasal 2, receptor 73
Synonyms EG620928
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.172) question?
Stock # R9159 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 85506755-85525146 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 85521931 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 136 (V136E)
Ref Sequence ENSEMBL: ENSMUSP00000076687 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077478]
AlphaFold D3Z7M3
Predicted Effect possibly damaging
Transcript: ENSMUST00000077478
AA Change: V136E

PolyPhen 2 Score 0.902 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000076687
Gene: ENSMUSG00000070458
AA Change: V136E

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 465 1.4e-30 PFAM
Pfam:NCD3G 508 560 5.9e-21 PFAM
Pfam:7tm_3 590 827 4.4e-51 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 97% (72/74)
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930012K11Rik A T 14: 70,394,238 (GRCm39) M179K probably benign Het
A030003K21Rik A G 1: 82,920,787 (GRCm39) V86A unknown Het
AC133488.1 A T 16: 18,440,075 (GRCm39) V363E probably benign Het
Adamts16 A G 13: 70,901,408 (GRCm39) S890P probably benign Het
Adgrf4 A G 17: 42,973,293 (GRCm39) V685A probably benign Het
Aff1 T A 5: 103,990,131 (GRCm39) M867K possibly damaging Het
Apba3 T A 10: 81,106,867 (GRCm39) S225T Het
Aplp1 T A 7: 30,141,775 (GRCm39) T228S probably benign Het
Arhgap18 A G 10: 26,730,886 (GRCm39) D188G probably benign Het
BC024063 T A 10: 81,944,906 (GRCm39) S175R possibly damaging Het
Bloc1s6 T G 2: 122,580,548 (GRCm39) S2R probably damaging Het
Cd209b A G 8: 3,974,245 (GRCm39) I119T possibly damaging Het
Cdk8 T C 5: 146,168,549 (GRCm39) V16A probably damaging Het
Cep295 A G 9: 15,252,904 (GRCm39) M308T probably benign Het
Cfap53 T A 18: 74,416,272 (GRCm39) Y2N probably damaging Het
Col28a1 T A 6: 8,014,993 (GRCm39) D804V probably damaging Het
Csta3 G A 16: 36,038,069 (GRCm39) V69I probably benign Het
Cyp2c40 A T 19: 39,762,317 (GRCm39) D443E probably damaging Het
Cyp2d9 A G 15: 82,338,572 (GRCm39) D202G possibly damaging Het
Dchs1 G A 7: 105,415,126 (GRCm39) A686V probably benign Het
Egf A T 3: 129,472,026 (GRCm39) N1199K probably benign Het
Eva1a A G 6: 82,068,855 (GRCm39) R61G possibly damaging Het
Exoc6 T A 19: 37,597,478 (GRCm39) D626E probably benign Het
Exosc10 T C 4: 148,663,916 (GRCm39) probably null Het
Firrm A G 1: 163,814,514 (GRCm39) I143T probably damaging Het
Gm12888 T C 4: 121,176,600 (GRCm39) Q67R probably null Het
Gm16485 A G 9: 8,972,319 (GRCm39) S62G unknown Het
Gng4 T C 13: 13,999,896 (GRCm39) I55T probably damaging Het
Gpihbp1 A G 15: 75,469,830 (GRCm39) S182G possibly damaging Het
Hax1 T C 3: 89,903,127 (GRCm39) R251G probably damaging Het
Igf2bp2 G A 16: 21,900,502 (GRCm39) T213I probably damaging Het
Il23a T A 10: 128,133,427 (GRCm39) K66* probably null Het
Itga2 A T 13: 115,014,298 (GRCm39) L210* probably null Het
Ltbp2 G A 12: 84,837,864 (GRCm39) P1192L probably benign Het
Matr3 T A 18: 35,712,355 (GRCm39) M389K possibly damaging Het
Mettl15 T C 2: 108,923,444 (GRCm39) D326G probably damaging Het
Mta1 T A 12: 113,100,025 (GRCm39) V645E probably damaging Het
Muc5ac T C 7: 141,363,529 (GRCm39) I2280T unknown Het
Naa15 T A 3: 51,358,802 (GRCm39) N362K probably benign Het
Necab2 T C 8: 120,189,303 (GRCm39) Y158H probably damaging Het
Nphp3 T A 9: 103,897,980 (GRCm39) L523Q probably damaging Het
Nphs1 T G 7: 30,165,026 (GRCm39) F540V possibly damaging Het
Or2av9 A G 11: 58,381,350 (GRCm39) V77A probably damaging Het
Or2k2 A G 4: 58,785,320 (GRCm39) I134T probably benign Het
Or5p55 A T 7: 107,567,524 (GRCm39) R307* probably null Het
Ppa1 A T 10: 61,496,784 (GRCm39) I91F probably damaging Het
Prdm6 C A 18: 53,598,019 (GRCm39) A127D unknown Het
Prdm8 T C 5: 98,334,175 (GRCm39) F581L probably damaging Het
Rbbp6 T C 7: 122,589,428 (GRCm39) I372T probably damaging Het
Rnf144b A G 13: 47,396,348 (GRCm39) I228M probably damaging Het
Rsf1 CG CGACGGCGGGG 7: 97,229,115 (GRCm39) probably benign Het
Setd2 T C 9: 110,374,385 (GRCm39) probably null Het
Sez6l T C 5: 112,613,824 (GRCm39) H441R possibly damaging Het
Shbg G A 11: 69,506,430 (GRCm39) L327F probably benign Het
Sik3 C T 9: 46,123,539 (GRCm39) Q1113* probably null Het
Smad2 T A 18: 76,395,573 (GRCm39) I4N possibly damaging Het
Spata31h1 G A 10: 82,118,524 (GRCm39) R4829* probably null Het
Sult2b1 T A 7: 45,391,534 (GRCm39) E84V probably damaging Het
Tbc1d8 A G 1: 39,444,474 (GRCm39) Y162H Het
Tedc2 A G 17: 24,436,705 (GRCm39) L308P probably damaging Het
Tmc5 T C 7: 118,233,264 (GRCm39) V26A probably benign Het
Tmem120b T A 5: 123,242,566 (GRCm39) N181K possibly damaging Het
Tmem229b T G 12: 79,011,448 (GRCm39) N161T possibly damaging Het
Tmem43 A C 6: 91,459,291 (GRCm39) D254A probably benign Het
Trpv6 T C 6: 41,603,074 (GRCm39) D266G probably benign Het
Tspan9 A G 6: 127,943,717 (GRCm39) I102T possibly damaging Het
Ung A G 5: 114,270,166 (GRCm39) probably benign Het
Upp2 C T 2: 58,667,996 (GRCm39) H230Y probably damaging Het
Vmn1r184 G A 7: 25,966,545 (GRCm39) S97N possibly damaging Het
Wdr20rt T C 12: 65,272,918 (GRCm39) V127A probably damaging Het
Yme1l1 T A 2: 23,063,058 (GRCm39) F210I probably damaging Het
Yrdc T C 4: 124,747,811 (GRCm39) probably null Het
Zfhx4 G T 3: 5,464,312 (GRCm39) R1515L probably damaging Het
Zfhx4 C T 3: 5,466,217 (GRCm39) P2150L probably damaging Het
Zfp267 C A 3: 36,219,902 (GRCm39) H642N possibly damaging Het
Zfp988 C T 4: 147,416,450 (GRCm39) P295S possibly damaging Het
Other mutations in Vmn2r73
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Vmn2r73 APN 7 85,506,795 (GRCm39) missense
IGL01151:Vmn2r73 APN 7 85,507,086 (GRCm39) missense probably damaging 0.99
IGL01408:Vmn2r73 APN 7 85,521,455 (GRCm39) missense probably benign 0.45
IGL01505:Vmn2r73 APN 7 85,507,267 (GRCm39) nonsense probably null
IGL01731:Vmn2r73 APN 7 85,506,757 (GRCm39) makesense probably null
IGL01818:Vmn2r73 APN 7 85,519,109 (GRCm39) splice site probably benign
IGL02236:Vmn2r73 APN 7 85,521,902 (GRCm39) missense probably benign 0.00
IGL02265:Vmn2r73 APN 7 85,520,847 (GRCm39) missense probably benign 0.02
IGL02266:Vmn2r73 APN 7 85,525,007 (GRCm39) missense possibly damaging 0.52
IGL02276:Vmn2r73 APN 7 85,518,980 (GRCm39) critical splice donor site probably null
IGL02284:Vmn2r73 APN 7 85,507,123 (GRCm39) missense possibly damaging 0.92
IGL02380:Vmn2r73 APN 7 85,507,383 (GRCm39) missense probably benign 0.00
IGL02466:Vmn2r73 APN 7 85,522,084 (GRCm39) missense probably damaging 1.00
IGL03172:Vmn2r73 APN 7 85,507,495 (GRCm39) missense probably benign 0.01
IGL03179:Vmn2r73 APN 7 85,519,468 (GRCm39) missense probably benign 0.04
G1Funyon:Vmn2r73 UTSW 7 85,507,510 (GRCm39) missense probably benign 0.00
R0077:Vmn2r73 UTSW 7 85,525,075 (GRCm39) missense probably benign 0.00
R0311:Vmn2r73 UTSW 7 85,520,997 (GRCm39) missense probably benign
R0413:Vmn2r73 UTSW 7 85,521,087 (GRCm39) missense possibly damaging 0.68
R0494:Vmn2r73 UTSW 7 85,522,140 (GRCm39) missense probably benign
R1523:Vmn2r73 UTSW 7 85,519,486 (GRCm39) missense probably benign 0.02
R1618:Vmn2r73 UTSW 7 85,525,120 (GRCm39) nonsense probably null
R1667:Vmn2r73 UTSW 7 85,506,889 (GRCm39) missense probably benign 0.00
R1728:Vmn2r73 UTSW 7 85,507,086 (GRCm39) missense probably damaging 1.00
R1729:Vmn2r73 UTSW 7 85,507,086 (GRCm39) missense probably damaging 1.00
R1747:Vmn2r73 UTSW 7 85,507,375 (GRCm39) missense probably damaging 1.00
R1784:Vmn2r73 UTSW 7 85,507,086 (GRCm39) missense probably damaging 1.00
R2152:Vmn2r73 UTSW 7 85,506,936 (GRCm39) missense probably benign 0.03
R2395:Vmn2r73 UTSW 7 85,506,975 (GRCm39) missense probably damaging 1.00
R2415:Vmn2r73 UTSW 7 85,521,431 (GRCm39) missense probably damaging 1.00
R2926:Vmn2r73 UTSW 7 85,520,871 (GRCm39) missense probably benign 0.17
R3719:Vmn2r73 UTSW 7 85,519,582 (GRCm39) missense probably damaging 1.00
R3766:Vmn2r73 UTSW 7 85,521,198 (GRCm39) missense probably benign
R3838:Vmn2r73 UTSW 7 85,507,258 (GRCm39) missense probably benign 0.00
R3890:Vmn2r73 UTSW 7 85,507,144 (GRCm39) missense probably benign
R4030:Vmn2r73 UTSW 7 85,521,044 (GRCm39) missense possibly damaging 0.92
R4247:Vmn2r73 UTSW 7 85,521,883 (GRCm39) missense probably damaging 0.99
R4409:Vmn2r73 UTSW 7 85,520,768 (GRCm39) missense probably damaging 0.97
R4427:Vmn2r73 UTSW 7 85,506,981 (GRCm39) missense probably damaging 1.00
R4430:Vmn2r73 UTSW 7 85,519,449 (GRCm39) missense probably benign
R4552:Vmn2r73 UTSW 7 85,525,055 (GRCm39) missense probably benign 0.12
R4779:Vmn2r73 UTSW 7 85,520,923 (GRCm39) nonsense probably null
R4906:Vmn2r73 UTSW 7 85,506,829 (GRCm39) missense probably damaging 0.99
R4942:Vmn2r73 UTSW 7 85,519,582 (GRCm39) missense probably damaging 1.00
R5280:Vmn2r73 UTSW 7 85,507,155 (GRCm39) missense probably damaging 0.98
R5344:Vmn2r73 UTSW 7 85,525,046 (GRCm39) missense probably benign 0.00
R5478:Vmn2r73 UTSW 7 85,518,996 (GRCm39) missense probably damaging 1.00
R5527:Vmn2r73 UTSW 7 85,507,575 (GRCm39) missense possibly damaging 0.65
R5691:Vmn2r73 UTSW 7 85,507,299 (GRCm39) missense probably damaging 1.00
R5826:Vmn2r73 UTSW 7 85,524,956 (GRCm39) missense possibly damaging 0.77
R6018:Vmn2r73 UTSW 7 85,521,875 (GRCm39) missense possibly damaging 0.48
R6082:Vmn2r73 UTSW 7 85,507,429 (GRCm39) missense probably benign 0.00
R6111:Vmn2r73 UTSW 7 85,520,997 (GRCm39) missense probably benign
R6233:Vmn2r73 UTSW 7 85,519,099 (GRCm39) missense probably benign 0.00
R6278:Vmn2r73 UTSW 7 85,522,140 (GRCm39) missense probably benign
R6283:Vmn2r73 UTSW 7 85,521,049 (GRCm39) missense probably benign 0.00
R6307:Vmn2r73 UTSW 7 85,506,828 (GRCm39) missense probably damaging 1.00
R6413:Vmn2r73 UTSW 7 85,519,544 (GRCm39) nonsense probably null
R6782:Vmn2r73 UTSW 7 85,519,563 (GRCm39) missense probably benign 0.00
R6884:Vmn2r73 UTSW 7 85,507,213 (GRCm39) missense probably benign 0.05
R6921:Vmn2r73 UTSW 7 85,507,446 (GRCm39) missense probably benign 0.27
R7169:Vmn2r73 UTSW 7 85,507,663 (GRCm39) nonsense probably null
R7206:Vmn2r73 UTSW 7 85,522,075 (GRCm39) missense probably benign 0.03
R7311:Vmn2r73 UTSW 7 85,521,192 (GRCm39) missense possibly damaging 0.80
R7650:Vmn2r73 UTSW 7 85,521,147 (GRCm39) missense probably benign
R7811:Vmn2r73 UTSW 7 85,524,956 (GRCm39) missense possibly damaging 0.77
R8263:Vmn2r73 UTSW 7 85,507,619 (GRCm39) missense probably benign
R8301:Vmn2r73 UTSW 7 85,507,510 (GRCm39) missense probably benign 0.00
R8341:Vmn2r73 UTSW 7 85,507,128 (GRCm39) missense probably benign 0.01
R8500:Vmn2r73 UTSW 7 85,519,638 (GRCm39) missense probably benign 0.01
R8673:Vmn2r73 UTSW 7 85,521,902 (GRCm39) missense probably benign 0.01
R8719:Vmn2r73 UTSW 7 85,521,095 (GRCm39) missense probably damaging 0.96
R8783:Vmn2r73 UTSW 7 85,507,668 (GRCm39) missense probably damaging 0.96
R8828:Vmn2r73 UTSW 7 85,521,179 (GRCm39) missense probably damaging 0.98
R8860:Vmn2r73 UTSW 7 85,522,149 (GRCm39) splice site probably benign
R9002:Vmn2r73 UTSW 7 85,507,284 (GRCm39) missense probably benign 0.32
R9008:Vmn2r73 UTSW 7 85,521,904 (GRCm39) missense probably damaging 0.96
R9180:Vmn2r73 UTSW 7 85,507,123 (GRCm39) missense probably benign 0.07
R9198:Vmn2r73 UTSW 7 85,518,987 (GRCm39) missense probably benign 0.01
R9329:Vmn2r73 UTSW 7 85,519,073 (GRCm39) missense probably benign
R9448:Vmn2r73 UTSW 7 85,522,027 (GRCm39) missense probably benign 0.00
R9463:Vmn2r73 UTSW 7 85,506,795 (GRCm39) missense
R9589:Vmn2r73 UTSW 7 85,519,659 (GRCm39) missense probably benign 0.03
X0023:Vmn2r73 UTSW 7 85,507,664 (GRCm39) missense probably benign 0.31
Z1176:Vmn2r73 UTSW 7 85,521,176 (GRCm39) missense probably damaging 0.99
Z1177:Vmn2r73 UTSW 7 85,521,480 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AATACTGCGGATCCCTATTCC -3'
(R):5'- GTTTTCAGCGTGACACCCAAG -3'

Sequencing Primer
(F):5'- GCGGATCCCTATTCCCATTTATG -3'
(R):5'- CAAGACCAACCATTTGATTTTCTCTG -3'
Posted On 2022-01-20