Incidental Mutation 'R0655:Vmn2r72'
ID 62484
Institutional Source Beutler Lab
Gene Symbol Vmn2r72
Ensembl Gene ENSMUSG00000051877
Gene Name vomeronasal 2, receptor 72
Synonyms EG244114, Vmn2r72-ps
MMRRC Submission 038840-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.089) question?
Stock # R0655 (G1)
Quality Score 136
Status Not validated
Chromosome 7
Chromosomal Location 85386992-85404189 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 85387319 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 748 (C748*)
Ref Sequence ENSEMBL: ENSMUSP00000133014 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063425]
AlphaFold D3Z4N8
Predicted Effect probably null
Transcript: ENSMUST00000063425
AA Change: C748*
SMART Domains Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877
AA Change: C748*

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
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 99.0%
  • 10x: 97.7%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 G C 17: 36,268,737 (GRCm39) I757M probably benign Het
Abtb3 A G 10: 85,481,390 (GRCm39) T931A probably damaging Het
Atg16l1 T A 1: 87,694,551 (GRCm39) I76N probably damaging Het
Baz1b T A 5: 135,271,284 (GRCm39) I1289N probably benign Het
Bcl2l15 T A 3: 103,740,285 (GRCm39) probably null Het
Cbl G T 9: 44,070,049 (GRCm39) T566K probably damaging Het
Cd96 T C 16: 45,919,482 (GRCm39) K180E probably benign Het
Cpxm2 G A 7: 131,656,549 (GRCm39) T571I possibly damaging Het
Cyp2a12 A T 7: 26,736,046 (GRCm39) Y485F probably benign Het
Cyp4f17 T A 17: 32,743,871 (GRCm39) Y350N possibly damaging Het
Dstn T A 2: 143,780,342 (GRCm39) I14N probably damaging Het
Eea1 A G 10: 95,831,460 (GRCm39) S184G probably benign Het
Eif1a G T 18: 46,741,130 (GRCm39) G122C probably damaging Het
Esf1 T A 2: 139,990,799 (GRCm39) T562S probably benign Het
Fem1c G A 18: 46,638,227 (GRCm39) R592C probably benign Het
Fig4 T C 10: 41,161,673 (GRCm39) N30S probably damaging Het
Gria2 C A 3: 80,639,377 (GRCm39) E212* probably null Het
Gsdmc2 C T 15: 63,699,622 (GRCm39) A269T probably benign Het
Herc4 T C 10: 63,109,350 (GRCm39) V195A probably benign Het
Hivep1 T C 13: 42,321,061 (GRCm39) S2123P probably damaging Het
Hspa4 T C 11: 53,160,519 (GRCm39) E519G probably benign Het
Htr2b A G 1: 86,038,565 (GRCm39) S14P probably benign Het
Ifit1 T C 19: 34,625,047 (GRCm39) V61A probably damaging Het
Ifitm1 C A 7: 140,549,449 (GRCm39) F77L probably benign Het
Matn2 T C 15: 34,345,346 (GRCm39) S118P probably benign Het
Mtmr3 C A 11: 4,438,610 (GRCm39) D615Y probably damaging Het
Mtss1 C A 15: 58,953,351 (GRCm39) C9F probably damaging Het
Muc5b A T 7: 141,417,679 (GRCm39) I3542F probably benign Het
Nwd2 T C 5: 63,948,928 (GRCm39) S167P possibly damaging Het
Or1e34 T C 11: 73,778,631 (GRCm39) D189G possibly damaging Het
Or2ag1b A T 7: 106,288,632 (GRCm39) F102Y probably damaging Het
Or8b54 C T 9: 38,686,850 (GRCm39) Q100* probably null Het
Oscp1 T C 4: 125,952,526 (GRCm39) L18P probably damaging Het
Pax5 A G 4: 44,537,462 (GRCm39) S297P probably damaging Het
Phldb3 A T 7: 24,323,797 (GRCm39) D476V probably benign Het
Phlpp2 A T 8: 110,622,219 (GRCm39) I154L probably benign Het
Prx T A 7: 27,216,846 (GRCm39) V449E probably damaging Het
Psd3 A G 8: 68,416,341 (GRCm39) S519P probably benign Het
Rnf138 T G 18: 21,143,840 (GRCm39) V128G probably benign Het
Safb T A 17: 56,904,803 (GRCm39) S209T probably benign Het
Sbno1 C A 5: 124,514,212 (GRCm39) V1327L possibly damaging Het
Scarb1 A G 5: 125,377,504 (GRCm39) V176A probably damaging Het
Scd4 A G 19: 44,327,407 (GRCm39) H161R possibly damaging Het
Selenoo T A 15: 88,979,858 (GRCm39) H335Q probably damaging Het
Slfn8 A G 11: 82,894,647 (GRCm39) F664S probably benign Het
Spef2 T C 15: 9,626,217 (GRCm39) I1116M possibly damaging Het
Taf2 G A 15: 54,901,690 (GRCm39) R835W probably damaging Het
Tdrd9 A G 12: 112,006,899 (GRCm39) E921G probably damaging Het
Tectb G A 19: 55,178,302 (GRCm39) G234S possibly damaging Het
Tmc1 C T 19: 20,776,540 (GRCm39) M606I probably damaging Het
Tmed10 T A 12: 85,390,291 (GRCm39) I88F probably damaging Het
Tnfrsf11a G A 1: 105,735,880 (GRCm39) V31I unknown Het
Trp53inp2 G T 2: 155,228,088 (GRCm39) G98* probably null Het
Tssc4 A G 7: 142,623,782 (GRCm39) D30G probably damaging Het
Uaca T C 9: 60,779,311 (GRCm39) Y1233H probably benign Het
Unc13c G A 9: 73,838,235 (GRCm39) T872I probably damaging Het
Unc80 A G 1: 66,542,940 (GRCm39) H398R probably damaging Het
Vmn1r64 G A 7: 5,887,207 (GRCm39) T112I probably benign Het
Vmn1r85 A G 7: 12,818,650 (GRCm39) Y165H probably damaging Het
Wdr17 A G 8: 55,102,233 (GRCm39) W929R probably damaging Het
Yeats2 A T 16: 20,012,574 (GRCm39) K591* probably null Het
Zbtb9 T A 17: 27,193,074 (GRCm39) S160T probably damaging Het
Znfx1 T A 2: 166,898,827 (GRCm39) R32S probably damaging Het
Zng1 T C 19: 24,930,684 (GRCm39) M122V possibly damaging 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
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
R1172:Vmn2r72 UTSW 7 85,401,152 (GRCm39) missense probably damaging 1.00
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 PCR Primer
(F):5'- GCCCTGCACTTGATGCCAAGATAC -3'
(R):5'- TGGTCATCCCACTACGGTCATCTG -3'

Sequencing Primer
(F):5'- TTCCACAGCAACCATAGTCTTG -3'
(R):5'- AGCAGACCACTTTTGCCATTG -3'
Posted On 2013-07-30