Incidental Mutation 'R7266:Vmn2r72'
ID 564928
Institutional Source Beutler Lab
Gene Symbol Vmn2r72
Ensembl Gene ENSMUSG00000051877
Gene Name vomeronasal 2, receptor 72
Synonyms Vmn2r72-ps, EG244114
MMRRC Submission 045389-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.113) question?
Stock # R7266 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 85737784-85754981 bp(-) (GRCm38)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 85738274 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Stop codon at position 694 (S694*)
Ref Sequence ENSEMBL: ENSMUSP00000133014 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063425]
AlphaFold D3Z4N8
Predicted Effect probably null
Transcript: ENSMUST00000063425
AA Change: S694*
SMART Domains Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877
AA Change: S694*

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: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam18 T A 8: 24,667,623 (GRCm38) I104F probably benign Het
Adgrg7 C T 16: 56,770,311 (GRCm38) V166I probably benign Het
Agfg1 G T 1: 82,882,245 (GRCm38) V278L probably benign Het
Alpk3 A G 7: 81,092,580 (GRCm38) E715G possibly damaging Het
Ap2m1 A G 16: 20,543,345 (GRCm38) Y401C probably damaging Het
Arhgef28 C T 13: 97,965,452 (GRCm38) S838N probably benign Het
Ash2l A T 8: 25,827,205 (GRCm38) Y373* probably null Het
Best2 C T 8: 85,007,764 (GRCm38) V442I probably benign Het
Col4a2 T C 8: 11,425,542 (GRCm38) probably null Het
Fat2 T A 11: 55,285,030 (GRCm38) D1619V probably damaging Het
Fer1l6 A T 15: 58,627,597 (GRCm38) N1272I probably benign Het
Gcc1 T A 6: 28,417,996 (GRCm38) *779C probably null Het
Gm12216 G A 11: 53,859,251 (GRCm38) probably benign Het
Gm17657 C A 17: 29,519,373 (GRCm38) V140L probably benign Het
Gm7102 A G 19: 61,175,535 (GRCm38) V154A possibly damaging Het
Grm2 C T 9: 106,647,171 (GRCm38) V311I Het
Immt T A 6: 71,874,705 (GRCm38) D683E probably benign Het
Itga8 T G 2: 12,232,901 (GRCm38) D336A probably damaging Het
Jhy T C 9: 40,961,157 (GRCm38) T19A probably benign Het
Kcnq2 T C 2: 181,135,092 (GRCm38) M1V probably null Het
Kctd17 A T 15: 78,433,014 (GRCm38) I117F probably damaging Het
Lrp6 T C 6: 134,507,401 (GRCm38) T420A probably damaging Het
Manba T C 3: 135,517,912 (GRCm38) S187P probably damaging Het
Mef2b A T 8: 70,164,288 (GRCm38) D13V probably damaging Het
Mical2 T C 7: 112,303,756 (GRCm38) F145L probably damaging Het
Mphosph8 T A 14: 56,685,040 (GRCm38) D551E possibly damaging Het
Myo10 C G 15: 25,782,981 (GRCm38) R1170G probably damaging Het
Myo16 A C 8: 10,272,687 (GRCm38) Q39P unknown Het
Myo1f A G 17: 33,601,694 (GRCm38) E837G probably benign Het
Nell2 T A 15: 95,435,393 (GRCm38) I128F possibly damaging Het
Olfr1357 A G 10: 78,612,614 (GRCm38) V9A probably benign Het
Pcdh15 A T 10: 74,379,390 (GRCm38) R659* probably null Het
Pcdhga1 A G 18: 37,839,975 (GRCm38) Q881R possibly damaging Het
Plekhm2 T G 4: 141,642,459 (GRCm38) E75A possibly damaging Het
Prc1 A G 7: 80,307,657 (GRCm38) K357E possibly damaging Het
Pxk T A 14: 8,146,220 (GRCm38) C377S probably benign Het
Ralgapa2 T C 2: 146,334,568 (GRCm38) E1696G probably damaging Het
Rbbp6 T A 7: 123,001,367 (GRCm38) S1532R unknown Het
Scn5a G T 9: 119,562,560 (GRCm38) A22E probably benign Het
Sctr G A 1: 120,022,225 (GRCm38) R48Q probably benign Het
Siae T C 9: 37,623,013 (GRCm38) V115A probably damaging Het
Slc16a6 A G 11: 109,453,281 (GRCm38) C563R probably benign Het
Sntg1 A C 1: 8,682,019 (GRCm38) V58G possibly damaging Het
Snx11 C T 11: 96,773,159 (GRCm38) V36M probably damaging Het
Stk3 C A 15: 34,959,036 (GRCm38) S330I probably benign Het
Synpo A G 18: 60,629,559 (GRCm38) F92S probably benign Het
Tle1 A G 4: 72,139,687 (GRCm38) probably null Het
Tmem117 A G 15: 94,931,803 (GRCm38) D173G possibly damaging Het
Tmprss5 T C 9: 49,114,541 (GRCm38) W338R probably benign Het
Tnfrsf19 T C 14: 60,974,698 (GRCm38) T168A possibly damaging Het
Trhde C T 10: 114,800,871 (GRCm38) G144S possibly damaging Het
Trim56 G T 5: 137,114,243 (GRCm38) Q140K probably damaging Het
Ttn C T 2: 76,732,574 (GRCm38) V28679M probably damaging Het
Ubxn8 G A 8: 33,623,203 (GRCm38) R208C probably damaging Het
Wdr38 T A 2: 39,000,264 (GRCm38) W137R probably damaging Het
Zdhhc6 G T 19: 55,304,500 (GRCm38) N271K probably damaging Het
Zfyve9 A G 4: 108,718,547 (GRCm38) S446P possibly damaging Het
Zmynd8 T C 2: 165,807,572 (GRCm38) Q867R possibly damaging Het
Zswim3 T C 2: 164,820,482 (GRCm38) I294T probably benign Het
Other mutations in Vmn2r72
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00931:Vmn2r72 APN 7 85,749,646 (GRCm38) missense probably benign 0.01
IGL01019:Vmn2r72 APN 7 85,738,334 (GRCm38) missense probably benign 0.26
IGL01445:Vmn2r72 APN 7 85,749,646 (GRCm38) missense probably benign 0.06
IGL02076:Vmn2r72 APN 7 85,738,367 (GRCm38) missense probably damaging 1.00
IGL02082:Vmn2r72 APN 7 85,738,166 (GRCm38) missense probably benign 0.00
IGL02086:Vmn2r72 APN 7 85,738,166 (GRCm38) missense probably benign 0.00
IGL02089:Vmn2r72 APN 7 85,738,166 (GRCm38) missense probably benign 0.00
IGL02125:Vmn2r72 APN 7 85,750,711 (GRCm38) missense probably benign 0.00
IGL02146:Vmn2r72 APN 7 85,737,962 (GRCm38) missense probably damaging 1.00
IGL02272:Vmn2r72 APN 7 85,750,693 (GRCm38) missense probably benign
IGL02514:Vmn2r72 APN 7 85,738,699 (GRCm38) missense possibly damaging 0.90
IGL02662:Vmn2r72 APN 7 85,738,183 (GRCm38) missense probably benign 0.26
IGL02697:Vmn2r72 APN 7 85,738,671 (GRCm38) missense probably benign 0.36
IGL02733:Vmn2r72 APN 7 85,751,813 (GRCm38) missense probably benign 0.05
IGL03070:Vmn2r72 APN 7 85,752,041 (GRCm38) splice site probably benign
IGL03150:Vmn2r72 APN 7 85,751,176 (GRCm38) missense probably damaging 1.00
IGL03159:Vmn2r72 APN 7 85,754,954 (GRCm38) missense probably benign 0.05
IGL03333:Vmn2r72 APN 7 85,750,867 (GRCm38) missense probably benign 0.10
R0081:Vmn2r72 UTSW 7 85,751,836 (GRCm38) missense probably benign 0.01
R0090:Vmn2r72 UTSW 7 85,754,876 (GRCm38) missense probably benign
R0655:Vmn2r72 UTSW 7 85,738,111 (GRCm38) nonsense probably null
R0778:Vmn2r72 UTSW 7 85,749,739 (GRCm38) missense probably benign 0.00
R1169:Vmn2r72 UTSW 7 85,751,309 (GRCm38) missense probably benign 0.01
R1172:Vmn2r72 UTSW 7 85,751,944 (GRCm38) missense probably damaging 1.00
R1173:Vmn2r72 UTSW 7 85,751,944 (GRCm38) missense probably damaging 1.00
R1175:Vmn2r72 UTSW 7 85,751,944 (GRCm38) missense probably damaging 1.00
R1248:Vmn2r72 UTSW 7 85,749,188 (GRCm38) missense probably benign 0.02
R1302:Vmn2r72 UTSW 7 85,738,257 (GRCm38) missense probably damaging 1.00
R1506:Vmn2r72 UTSW 7 85,749,211 (GRCm38) missense probably benign
R1632:Vmn2r72 UTSW 7 85,751,792 (GRCm38) missense probably benign 0.13
R1775:Vmn2r72 UTSW 7 85,738,170 (GRCm38) missense probably benign 0.01
R1962:Vmn2r72 UTSW 7 85,749,161 (GRCm38) missense probably benign 0.00
R2201:Vmn2r72 UTSW 7 85,738,236 (GRCm38) missense probably benign 0.12
R2290:Vmn2r72 UTSW 7 85,738,341 (GRCm38) missense probably damaging 1.00
R2327:Vmn2r72 UTSW 7 85,738,256 (GRCm38) missense probably damaging 1.00
R2424:Vmn2r72 UTSW 7 85,750,953 (GRCm38) missense probably damaging 1.00
R2655:Vmn2r72 UTSW 7 85,751,269 (GRCm38) missense possibly damaging 0.95
R2860:Vmn2r72 UTSW 7 85,750,836 (GRCm38) missense probably damaging 0.99
R2861:Vmn2r72 UTSW 7 85,750,836 (GRCm38) missense probably damaging 0.99
R2862:Vmn2r72 UTSW 7 85,750,836 (GRCm38) missense probably damaging 0.99
R3009:Vmn2r72 UTSW 7 85,749,642 (GRCm38) missense probably benign 0.00
R3797:Vmn2r72 UTSW 7 85,738,077 (GRCm38) missense probably benign 0.44
R3798:Vmn2r72 UTSW 7 85,738,077 (GRCm38) missense probably benign 0.44
R3902:Vmn2r72 UTSW 7 85,749,735 (GRCm38) missense possibly damaging 0.52
R3959:Vmn2r72 UTSW 7 85,751,131 (GRCm38) missense probably benign 0.36
R3974:Vmn2r72 UTSW 7 85,749,809 (GRCm38) missense probably damaging 1.00
R4399:Vmn2r72 UTSW 7 85,738,500 (GRCm38) missense probably damaging 1.00
R4421:Vmn2r72 UTSW 7 85,738,500 (GRCm38) missense probably damaging 1.00
R4426:Vmn2r72 UTSW 7 85,737,828 (GRCm38) nonsense probably null
R4522:Vmn2r72 UTSW 7 85,751,926 (GRCm38) missense probably benign 0.44
R4523:Vmn2r72 UTSW 7 85,751,926 (GRCm38) missense probably benign 0.44
R4533:Vmn2r72 UTSW 7 85,751,926 (GRCm38) missense probably benign 0.44
R4691:Vmn2r72 UTSW 7 85,737,911 (GRCm38) nonsense probably null
R4781:Vmn2r72 UTSW 7 85,737,861 (GRCm38) missense probably benign 0.14
R4863:Vmn2r72 UTSW 7 85,750,598 (GRCm38) missense possibly damaging 0.91
R4952:Vmn2r72 UTSW 7 85,751,109 (GRCm38) missense probably benign
R4991:Vmn2r72 UTSW 7 85,751,130 (GRCm38) missense probably damaging 0.99
R4995:Vmn2r72 UTSW 7 85,738,485 (GRCm38) missense probably damaging 1.00
R5095:Vmn2r72 UTSW 7 85,737,853 (GRCm38) missense probably damaging 0.98
R5174:Vmn2r72 UTSW 7 85,737,840 (GRCm38) missense probably benign 0.00
R5276:Vmn2r72 UTSW 7 85,738,254 (GRCm38) missense possibly damaging 0.90
R5395:Vmn2r72 UTSW 7 85,750,897 (GRCm38) missense possibly damaging 0.71
R5560:Vmn2r72 UTSW 7 85,751,942 (GRCm38) missense probably damaging 0.96
R5933:Vmn2r72 UTSW 7 85,737,850 (GRCm38) missense probably benign 0.05
R6033:Vmn2r72 UTSW 7 85,737,929 (GRCm38) missense probably damaging 1.00
R6033:Vmn2r72 UTSW 7 85,737,929 (GRCm38) missense probably damaging 1.00
R6354:Vmn2r72 UTSW 7 85,750,539 (GRCm38) critical splice donor site probably null
R6362:Vmn2r72 UTSW 7 85,751,174 (GRCm38) missense probably damaging 1.00
R6594:Vmn2r72 UTSW 7 85,749,684 (GRCm38) missense probably benign 0.32
R6794:Vmn2r72 UTSW 7 85,737,996 (GRCm38) missense probably damaging 1.00
R7113:Vmn2r72 UTSW 7 85,749,803 (GRCm38) splice site probably null
R7189:Vmn2r72 UTSW 7 85,754,917 (GRCm38) missense probably benign 0.36
R7323:Vmn2r72 UTSW 7 85,750,563 (GRCm38) missense probably benign
R7426:Vmn2r72 UTSW 7 85,751,140 (GRCm38) missense probably benign
R7606:Vmn2r72 UTSW 7 85,751,154 (GRCm38) missense possibly damaging 0.91
R7651:Vmn2r72 UTSW 7 85,751,938 (GRCm38) missense probably damaging 1.00
R7688:Vmn2r72 UTSW 7 85,754,890 (GRCm38) missense probably benign 0.32
R7753:Vmn2r72 UTSW 7 85,750,626 (GRCm38) missense probably damaging 1.00
R7843:Vmn2r72 UTSW 7 85,749,630 (GRCm38) missense probably benign 0.01
R8157:Vmn2r72 UTSW 7 85,751,233 (GRCm38) missense probably benign 0.09
R8254:Vmn2r72 UTSW 7 85,751,019 (GRCm38) missense probably damaging 1.00
R8389:Vmn2r72 UTSW 7 85,751,960 (GRCm38) missense probably damaging 0.99
R8444:Vmn2r72 UTSW 7 85,738,175 (GRCm38) missense probably benign
R8989:Vmn2r72 UTSW 7 85,754,926 (GRCm38) missense probably benign 0.10
R9015:Vmn2r72 UTSW 7 85,749,180 (GRCm38) missense probably benign 0.01
R9080:Vmn2r72 UTSW 7 85,738,256 (GRCm38) missense probably damaging 1.00
R9269:Vmn2r72 UTSW 7 85,751,203 (GRCm38) missense probably benign 0.03
R9317:Vmn2r72 UTSW 7 85,754,814 (GRCm38) missense probably benign 0.04
R9509:Vmn2r72 UTSW 7 85,754,867 (GRCm38) missense probably benign
Z1176:Vmn2r72 UTSW 7 85,749,191 (GRCm38) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GCCCATGTATCCAAGGACACAG -3'
(R):5'- TGCGTCTTCCTGAAACACAG -3'

Sequencing Primer
(F):5'- GTAGAAGGCAATCACTGAACCTTTG -3'
(R):5'- AAACTCTCAGCTATGTACTACTCATC -3'
Posted On 2019-06-26