Incidental Mutation 'R1172:Vmn2r72'
ID 99567
Institutional Source Beutler Lab
Gene Symbol Vmn2r72
Ensembl Gene ENSMUSG00000051877
Gene Name vomeronasal 2, receptor 72
Synonyms EG244114, Vmn2r72-ps
MMRRC Submission 039245-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.089) question?
Stock # R1172 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 85386992-85404189 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 85401152 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Valine at position 89 (E89V)
Ref Sequence ENSEMBL: ENSMUSP00000133014 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063425]
AlphaFold D3Z4N8
Predicted Effect probably damaging
Transcript: ENSMUST00000063425
AA Change: E89V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877
AA Change: E89V

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 82 469 2.3e-28 PFAM
Pfam:NCD3G 512 564 1.2e-18 PFAM
Pfam:7tm_3 594 832 4e-53 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.5%
Validation Efficiency 98% (62/63)
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Accsl A T 2: 93,696,589 (GRCm39) probably benign Het
Adam7 T G 14: 68,752,370 (GRCm39) K371N probably damaging Het
Adgrv1 A T 13: 81,705,182 (GRCm39) S1543T probably damaging Het
Agbl4 A T 4: 111,513,515 (GRCm39) probably benign Het
Arid1b T A 17: 5,389,575 (GRCm39) I1707N probably damaging Het
Atp10a T C 7: 58,453,514 (GRCm39) V864A probably benign Het
Bivm A G 1: 44,165,942 (GRCm39) T131A probably benign Het
Bst1 A G 5: 43,982,750 (GRCm39) probably null Het
C9orf72 C A 4: 35,218,630 (GRCm39) E76D probably damaging Het
Cblb T C 16: 52,006,603 (GRCm39) probably benign Het
Ccdc28b T C 4: 129,514,682 (GRCm39) probably benign Het
Cmas G T 6: 142,702,604 (GRCm39) G36C probably benign Het
Eml6 A G 11: 29,699,824 (GRCm39) S1771P possibly damaging Het
Epc1 A C 18: 6,490,525 (GRCm39) Y31D probably damaging Het
Fbn1 A T 2: 125,236,607 (GRCm39) C358S probably benign Het
Fbxl13 A T 5: 21,825,602 (GRCm39) probably benign Het
Fermt2 T C 14: 45,697,425 (GRCm39) D642G possibly damaging Het
Fmnl2 A T 2: 52,962,286 (GRCm39) N257I probably damaging Het
Fry G A 5: 150,404,959 (GRCm39) W793* probably null Het
Fsd2 T C 7: 81,209,518 (GRCm39) D108G probably benign Het
Glipr1l2 C A 10: 111,919,371 (GRCm39) L31I possibly damaging Het
Gm10608 CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA 9: 118,989,784 (GRCm39) probably null Het
Gm10801 C T 2: 98,494,252 (GRCm39) probably benign Het
Gm21718 T C 14: 51,553,348 (GRCm39) noncoding transcript Het
Gpld1 A G 13: 25,141,549 (GRCm39) probably null Het
Gtf3c2 A T 5: 31,325,419 (GRCm39) Y500N probably damaging Het
Hbs1l A G 10: 21,180,537 (GRCm39) D73G probably damaging Het
Idh1 G T 1: 65,200,319 (GRCm39) N348K probably benign Het
Kank4 T C 4: 98,653,806 (GRCm39) Y874C probably damaging Het
Lamc2 A T 1: 153,042,033 (GRCm39) S34T probably damaging Het
Laptm4a T C 12: 8,986,716 (GRCm39) V258A probably damaging Het
Lrrc19 A T 4: 94,526,626 (GRCm39) Y310* probably null Het
Map3k5 G A 10: 19,932,394 (GRCm39) probably benign Het
Map7 G A 10: 20,121,045 (GRCm39) E92K probably damaging Het
Mettl24 G A 10: 40,613,704 (GRCm39) A148T probably benign Het
Mosmo A G 7: 120,329,745 (GRCm39) Y122C probably benign Het
Ncr1 T A 7: 4,341,120 (GRCm39) I37N probably benign Het
Nkx3-1 T C 14: 69,429,434 (GRCm39) S151P probably damaging Het
Npm2 T A 14: 70,889,661 (GRCm39) K54* probably null Het
Npr1 T A 3: 90,368,689 (GRCm39) D457V probably benign Het
Nudt21 T C 8: 94,757,757 (GRCm39) probably benign Het
Pcnt A T 10: 76,228,878 (GRCm39) probably null Het
Pik3r4 G T 9: 105,540,373 (GRCm39) G754C probably damaging Het
Rftn2 A G 1: 55,250,376 (GRCm39) V123A probably damaging Het
Rpa1 A T 11: 75,203,219 (GRCm39) V392D probably damaging Het
Rxfp2 T C 5: 149,975,021 (GRCm39) V210A probably benign Het
Slc45a4 C T 15: 73,477,278 (GRCm39) probably benign Het
Syndig1l T A 12: 84,725,942 (GRCm39) probably null Het
Tctn1 G A 5: 122,389,752 (GRCm39) R257* probably null Het
Tenm4 A T 7: 96,497,251 (GRCm39) E1179V probably damaging Het
Txlnb A G 10: 17,718,504 (GRCm39) N445S probably benign Het
Tyrp1 C T 4: 80,763,105 (GRCm39) Q331* probably null Het
Ubap2l A T 3: 89,930,807 (GRCm39) S413T probably benign Het
Vdr A T 15: 97,767,214 (GRCm39) Y185N probably benign Het
Vmn2r66 G T 7: 84,654,799 (GRCm39) D503E probably benign Het
Vmn2r87 T C 10: 130,313,453 (GRCm39) T438A probably benign Het
Xrcc6 A G 15: 81,915,364 (GRCm39) D94G probably damaging Het
Ywhaq T C 12: 21,445,024 (GRCm39) N207S probably benign Het
Zfp185 A T X: 72,042,929 (GRCm39) E138D possibly damaging Het
Zfp981 G A 4: 146,622,221 (GRCm39) S382N probably benign Het
Other mutations in Vmn2r72
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00931:Vmn2r72 APN 7 85,398,854 (GRCm39) missense probably benign 0.01
IGL01019:Vmn2r72 APN 7 85,387,542 (GRCm39) missense probably benign 0.26
IGL01445:Vmn2r72 APN 7 85,398,854 (GRCm39) missense probably benign 0.06
IGL02076:Vmn2r72 APN 7 85,387,575 (GRCm39) missense probably damaging 1.00
IGL02082:Vmn2r72 APN 7 85,387,374 (GRCm39) missense probably benign 0.00
IGL02086:Vmn2r72 APN 7 85,387,374 (GRCm39) missense probably benign 0.00
IGL02089:Vmn2r72 APN 7 85,387,374 (GRCm39) missense probably benign 0.00
IGL02125:Vmn2r72 APN 7 85,399,919 (GRCm39) missense probably benign 0.00
IGL02146:Vmn2r72 APN 7 85,387,170 (GRCm39) missense probably damaging 1.00
IGL02272:Vmn2r72 APN 7 85,399,901 (GRCm39) missense probably benign
IGL02514:Vmn2r72 APN 7 85,387,907 (GRCm39) missense possibly damaging 0.90
IGL02662:Vmn2r72 APN 7 85,387,391 (GRCm39) missense probably benign 0.26
IGL02697:Vmn2r72 APN 7 85,387,879 (GRCm39) missense probably benign 0.36
IGL02733:Vmn2r72 APN 7 85,401,021 (GRCm39) missense probably benign 0.05
IGL03070:Vmn2r72 APN 7 85,401,249 (GRCm39) splice site probably benign
IGL03150:Vmn2r72 APN 7 85,400,384 (GRCm39) missense probably damaging 1.00
IGL03159:Vmn2r72 APN 7 85,404,162 (GRCm39) missense probably benign 0.05
IGL03333:Vmn2r72 APN 7 85,400,075 (GRCm39) missense probably benign 0.10
R0081:Vmn2r72 UTSW 7 85,401,044 (GRCm39) missense probably benign 0.01
R0090:Vmn2r72 UTSW 7 85,404,084 (GRCm39) missense probably benign
R0655:Vmn2r72 UTSW 7 85,387,319 (GRCm39) nonsense probably null
R0778:Vmn2r72 UTSW 7 85,398,947 (GRCm39) missense probably benign 0.00
R1169:Vmn2r72 UTSW 7 85,400,517 (GRCm39) missense probably benign 0.01
R1173:Vmn2r72 UTSW 7 85,401,152 (GRCm39) missense probably damaging 1.00
R1175:Vmn2r72 UTSW 7 85,401,152 (GRCm39) missense probably damaging 1.00
R1248:Vmn2r72 UTSW 7 85,398,396 (GRCm39) missense probably benign 0.02
R1302:Vmn2r72 UTSW 7 85,387,465 (GRCm39) missense probably damaging 1.00
R1506:Vmn2r72 UTSW 7 85,398,419 (GRCm39) missense probably benign
R1632:Vmn2r72 UTSW 7 85,401,000 (GRCm39) missense probably benign 0.13
R1775:Vmn2r72 UTSW 7 85,387,378 (GRCm39) missense probably benign 0.01
R1962:Vmn2r72 UTSW 7 85,398,369 (GRCm39) missense probably benign 0.00
R2201:Vmn2r72 UTSW 7 85,387,444 (GRCm39) missense probably benign 0.12
R2290:Vmn2r72 UTSW 7 85,387,549 (GRCm39) missense probably damaging 1.00
R2327:Vmn2r72 UTSW 7 85,387,464 (GRCm39) missense probably damaging 1.00
R2424:Vmn2r72 UTSW 7 85,400,161 (GRCm39) missense probably damaging 1.00
R2655:Vmn2r72 UTSW 7 85,400,477 (GRCm39) missense possibly damaging 0.95
R2860:Vmn2r72 UTSW 7 85,400,044 (GRCm39) missense probably damaging 0.99
R2861:Vmn2r72 UTSW 7 85,400,044 (GRCm39) missense probably damaging 0.99
R2862:Vmn2r72 UTSW 7 85,400,044 (GRCm39) missense probably damaging 0.99
R3009:Vmn2r72 UTSW 7 85,398,850 (GRCm39) missense probably benign 0.00
R3797:Vmn2r72 UTSW 7 85,387,285 (GRCm39) missense probably benign 0.44
R3798:Vmn2r72 UTSW 7 85,387,285 (GRCm39) missense probably benign 0.44
R3902:Vmn2r72 UTSW 7 85,398,943 (GRCm39) missense possibly damaging 0.52
R3959:Vmn2r72 UTSW 7 85,400,339 (GRCm39) missense probably benign 0.36
R3974:Vmn2r72 UTSW 7 85,399,017 (GRCm39) missense probably damaging 1.00
R4399:Vmn2r72 UTSW 7 85,387,708 (GRCm39) missense probably damaging 1.00
R4421:Vmn2r72 UTSW 7 85,387,708 (GRCm39) missense probably damaging 1.00
R4426:Vmn2r72 UTSW 7 85,387,036 (GRCm39) nonsense probably null
R4522:Vmn2r72 UTSW 7 85,401,134 (GRCm39) missense probably benign 0.44
R4523:Vmn2r72 UTSW 7 85,401,134 (GRCm39) missense probably benign 0.44
R4533:Vmn2r72 UTSW 7 85,401,134 (GRCm39) missense probably benign 0.44
R4691:Vmn2r72 UTSW 7 85,387,119 (GRCm39) nonsense probably null
R4781:Vmn2r72 UTSW 7 85,387,069 (GRCm39) missense probably benign 0.14
R4863:Vmn2r72 UTSW 7 85,399,806 (GRCm39) missense possibly damaging 0.91
R4952:Vmn2r72 UTSW 7 85,400,317 (GRCm39) missense probably benign
R4991:Vmn2r72 UTSW 7 85,400,338 (GRCm39) missense probably damaging 0.99
R4995:Vmn2r72 UTSW 7 85,387,693 (GRCm39) missense probably damaging 1.00
R5095:Vmn2r72 UTSW 7 85,387,061 (GRCm39) missense probably damaging 0.98
R5174:Vmn2r72 UTSW 7 85,387,048 (GRCm39) missense probably benign 0.00
R5276:Vmn2r72 UTSW 7 85,387,462 (GRCm39) missense possibly damaging 0.90
R5395:Vmn2r72 UTSW 7 85,400,105 (GRCm39) missense possibly damaging 0.71
R5560:Vmn2r72 UTSW 7 85,401,150 (GRCm39) missense probably damaging 0.96
R5933:Vmn2r72 UTSW 7 85,387,058 (GRCm39) missense probably benign 0.05
R6033:Vmn2r72 UTSW 7 85,387,137 (GRCm39) missense probably damaging 1.00
R6033:Vmn2r72 UTSW 7 85,387,137 (GRCm39) missense probably damaging 1.00
R6354:Vmn2r72 UTSW 7 85,399,747 (GRCm39) critical splice donor site probably null
R6362:Vmn2r72 UTSW 7 85,400,382 (GRCm39) missense probably damaging 1.00
R6594:Vmn2r72 UTSW 7 85,398,892 (GRCm39) missense probably benign 0.32
R6794:Vmn2r72 UTSW 7 85,387,204 (GRCm39) missense probably damaging 1.00
R7113:Vmn2r72 UTSW 7 85,399,011 (GRCm39) splice site probably null
R7189:Vmn2r72 UTSW 7 85,404,125 (GRCm39) missense probably benign 0.36
R7266:Vmn2r72 UTSW 7 85,387,482 (GRCm39) nonsense probably null
R7323:Vmn2r72 UTSW 7 85,399,771 (GRCm39) missense probably benign
R7426:Vmn2r72 UTSW 7 85,400,348 (GRCm39) missense probably benign
R7606:Vmn2r72 UTSW 7 85,400,362 (GRCm39) missense possibly damaging 0.91
R7651:Vmn2r72 UTSW 7 85,401,146 (GRCm39) missense probably damaging 1.00
R7688:Vmn2r72 UTSW 7 85,404,098 (GRCm39) missense probably benign 0.32
R7753:Vmn2r72 UTSW 7 85,399,834 (GRCm39) missense probably damaging 1.00
R7843:Vmn2r72 UTSW 7 85,398,838 (GRCm39) missense probably benign 0.01
R8157:Vmn2r72 UTSW 7 85,400,441 (GRCm39) missense probably benign 0.09
R8254:Vmn2r72 UTSW 7 85,400,227 (GRCm39) missense probably damaging 1.00
R8389:Vmn2r72 UTSW 7 85,401,168 (GRCm39) missense probably damaging 0.99
R8444:Vmn2r72 UTSW 7 85,387,383 (GRCm39) missense probably benign
R8989:Vmn2r72 UTSW 7 85,404,134 (GRCm39) missense probably benign 0.10
R9015:Vmn2r72 UTSW 7 85,398,388 (GRCm39) missense probably benign 0.01
R9080:Vmn2r72 UTSW 7 85,387,464 (GRCm39) missense probably damaging 1.00
R9269:Vmn2r72 UTSW 7 85,400,411 (GRCm39) missense probably benign 0.03
R9317:Vmn2r72 UTSW 7 85,404,022 (GRCm39) missense probably benign 0.04
R9509:Vmn2r72 UTSW 7 85,404,075 (GRCm39) missense probably benign
Z1176:Vmn2r72 UTSW 7 85,398,399 (GRCm39) missense probably damaging 0.99
Predicted Primers
Posted On 2014-01-15