Incidental Mutation 'R7682:Vmn2r11'
ID 592815
Institutional Source Beutler Lab
Gene Symbol Vmn2r11
Ensembl Gene ENSMUSG00000091450
Gene Name vomeronasal 2, receptor 11
Synonyms EG384219
MMRRC Submission 045748-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R7682 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 109194739-109207318 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 109195481 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 615 (V615G)
Ref Sequence ENSEMBL: ENSMUSP00000133218 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164875]
AlphaFold E9Q4X4
Predicted Effect probably benign
Transcript: ENSMUST00000164875
AA Change: V615G

PolyPhen 2 Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000133218
Gene: ENSMUSG00000091450
AA Change: V615G

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 167 475 1.6e-29 PFAM
Pfam:NCD3G 520 574 9.1e-19 PFAM
Pfam:7tm_3 607 842 4.6e-55 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (62/62)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310034C09Rik T A 16: 88,556,373 (GRCm39) S196T probably benign Het
Abcc5 T C 16: 20,186,803 (GRCm39) D977G probably damaging Het
Acot2 T C 12: 84,034,698 (GRCm39) V8A probably benign Het
Adamts9 T A 6: 92,857,679 (GRCm39) I870F possibly damaging Het
Adgrl3 G A 5: 81,942,407 (GRCm39) V1414I probably damaging Het
Aggf1 T C 13: 95,504,934 (GRCm39) K275R probably benign Het
Alpk1 T C 3: 127,466,195 (GRCm39) I1104V possibly damaging Het
Angptl7 A T 4: 148,582,539 (GRCm39) I119N probably damaging Het
Ank3 A T 10: 69,824,065 (GRCm39) E129D possibly damaging Het
Brca2 T A 5: 150,466,618 (GRCm39) H2127Q probably benign Het
Brd4 A G 17: 32,420,134 (GRCm39) F1008S unknown Het
Car2 T C 3: 14,953,025 (GRCm39) S56P probably damaging Het
Casp3 A G 8: 47,085,420 (GRCm39) Y41C probably benign Het
Ces4a A T 8: 105,873,297 (GRCm39) T381S probably benign Het
Clstn1 A G 4: 149,710,558 (GRCm39) T77A possibly damaging Het
Cul7 G T 17: 46,966,521 (GRCm39) V615L probably benign Het
Dnpep A G 1: 75,293,384 (GRCm39) F24L probably damaging Het
Efcab3 T A 11: 104,855,174 (GRCm39) probably null Het
Emsy G A 7: 98,239,905 (GRCm39) R1263W probably damaging Het
Fam124b A T 1: 80,191,282 (GRCm39) C34S possibly damaging Het
Fan1 C A 7: 64,022,512 (GRCm39) G247V probably benign Het
Fbxl9 C A 8: 106,041,916 (GRCm39) R304L possibly damaging Het
Glipr1l3 T G 10: 111,977,777 (GRCm39) H218P probably benign Het
Gm14305 T A 2: 176,412,703 (GRCm39) S198R probably benign Het
Gm14326 T C 2: 177,590,274 (GRCm39) Y29C probably damaging Het
Gm45713 C T 7: 44,783,426 (GRCm39) V147I probably benign Het
Gpr149 C T 3: 62,438,160 (GRCm39) D666N probably damaging Het
Gpr183 A G 14: 122,192,152 (GRCm39) I123T possibly damaging Het
Il7r A T 15: 9,513,013 (GRCm39) H165Q probably damaging Het
Krt73 A G 15: 101,710,480 (GRCm39) F85L probably benign Het
Lrrc8d A G 5: 105,960,657 (GRCm39) T356A probably damaging Het
Marco A G 1: 120,421,771 (GRCm39) probably null Het
Mettl14 T A 3: 123,177,253 (GRCm39) E49D possibly damaging Het
Mrap T A 16: 90,546,110 (GRCm39) probably null Het
Mrps34 C T 17: 25,114,852 (GRCm39) A152V probably benign Het
Nfasc T A 1: 132,501,511 (GRCm39) Y1163F unknown Het
Nfic T C 10: 81,256,334 (GRCm39) D110G probably damaging Het
Nip7 T C 8: 107,783,751 (GRCm39) V28A possibly damaging Het
Odam T C 5: 88,040,287 (GRCm39) F251S possibly damaging Het
Olfm5 T A 7: 103,810,979 (GRCm39) Q53L probably null Het
P2ry13 T G 3: 59,117,545 (GRCm39) M78L probably benign Het
Pacs1 T C 19: 5,202,727 (GRCm39) E385G probably damaging Het
Pip5k1b C T 19: 24,337,343 (GRCm39) G315D probably damaging Het
Pla2g4a C A 1: 149,762,022 (GRCm39) R145L probably damaging Het
Pramel26 A G 4: 143,537,290 (GRCm39) L347S probably benign Het
Rars1 T C 11: 35,719,579 (GRCm39) Q81R probably benign Het
Rassf7 A G 7: 140,797,847 (GRCm39) N296D probably damaging Het
Rcsd1 C T 1: 165,485,262 (GRCm39) A94T probably benign Het
Rgs8 T C 1: 153,566,668 (GRCm39) F73S probably damaging Het
Rilpl2 A C 5: 124,616,043 (GRCm39) Y36D probably damaging Het
Rpl10l A G 12: 66,331,004 (GRCm39) V43A probably benign Het
Sesn2 T C 4: 132,224,200 (GRCm39) I403V probably damaging Het
Slc10a4 C T 5: 73,164,453 (GRCm39) S15L unknown Het
Slc7a5 T C 8: 122,633,879 (GRCm39) Y156C probably damaging Het
Spata18 A G 5: 73,826,008 (GRCm39) H105R Het
Specc1l A G 10: 75,081,636 (GRCm39) D344G probably damaging Het
Syne1 A G 10: 5,112,461 (GRCm39) V415A probably benign Het
Thbs4 T G 13: 92,912,070 (GRCm39) D220A probably benign Het
Tmco5 T C 2: 116,716,752 (GRCm39) S152P probably benign Het
Tmem35b A T 4: 127,022,734 (GRCm39) D125V probably damaging Het
Trim17 A G 11: 58,857,634 (GRCm39) E155G possibly damaging Het
Vmn2r88 A T 14: 51,655,906 (GRCm39) Q705L Het
Vmn2r93 A G 17: 18,525,583 (GRCm39) R414G probably benign Het
Xirp2 T C 2: 67,339,193 (GRCm39) L478P probably damaging Het
Other mutations in Vmn2r11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00925:Vmn2r11 APN 5 109,194,885 (GRCm39) missense probably benign 0.00
IGL01677:Vmn2r11 APN 5 109,201,823 (GRCm39) missense possibly damaging 0.50
IGL02048:Vmn2r11 APN 5 109,202,658 (GRCm39) missense probably benign 0.00
IGL02559:Vmn2r11 APN 5 109,200,046 (GRCm39) missense probably damaging 0.98
IGL02879:Vmn2r11 APN 5 109,201,704 (GRCm39) missense possibly damaging 0.95
IGL03084:Vmn2r11 APN 5 109,207,209 (GRCm39) missense probably benign 0.00
IGL03163:Vmn2r11 APN 5 109,201,692 (GRCm39) missense probably benign 0.41
IGL03289:Vmn2r11 APN 5 109,196,788 (GRCm39) splice site probably benign
IGL03294:Vmn2r11 APN 5 109,201,935 (GRCm39) missense probably benign 0.22
R0233:Vmn2r11 UTSW 5 109,201,968 (GRCm39) missense probably benign 0.16
R0233:Vmn2r11 UTSW 5 109,201,968 (GRCm39) missense probably benign 0.16
R0421:Vmn2r11 UTSW 5 109,207,294 (GRCm39) missense probably benign 0.00
R0549:Vmn2r11 UTSW 5 109,199,963 (GRCm39) missense possibly damaging 0.80
R0628:Vmn2r11 UTSW 5 109,195,597 (GRCm39) missense possibly damaging 0.88
R1523:Vmn2r11 UTSW 5 109,201,707 (GRCm39) missense probably benign 0.25
R1660:Vmn2r11 UTSW 5 109,201,724 (GRCm39) missense possibly damaging 0.79
R1827:Vmn2r11 UTSW 5 109,199,938 (GRCm39) missense probably benign 0.01
R1913:Vmn2r11 UTSW 5 109,202,654 (GRCm39) missense probably benign
R2260:Vmn2r11 UTSW 5 109,201,657 (GRCm39) nonsense probably null
R2400:Vmn2r11 UTSW 5 109,199,928 (GRCm39) missense probably benign 0.03
R3933:Vmn2r11 UTSW 5 109,201,260 (GRCm39) missense probably damaging 0.97
R4091:Vmn2r11 UTSW 5 109,202,616 (GRCm39) critical splice donor site probably null
R4624:Vmn2r11 UTSW 5 109,200,101 (GRCm39) missense probably damaging 0.99
R4762:Vmn2r11 UTSW 5 109,195,436 (GRCm39) missense probably damaging 1.00
R5256:Vmn2r11 UTSW 5 109,202,658 (GRCm39) missense probably benign 0.26
R5370:Vmn2r11 UTSW 5 109,195,421 (GRCm39) missense probably damaging 1.00
R5419:Vmn2r11 UTSW 5 109,207,224 (GRCm39) missense possibly damaging 0.55
R5516:Vmn2r11 UTSW 5 109,195,032 (GRCm39) missense probably damaging 0.98
R5643:Vmn2r11 UTSW 5 109,194,869 (GRCm39) missense probably damaging 1.00
R5671:Vmn2r11 UTSW 5 109,202,772 (GRCm39) missense probably benign 0.03
R5679:Vmn2r11 UTSW 5 109,202,708 (GRCm39) missense probably benign 0.00
R5739:Vmn2r11 UTSW 5 109,207,114 (GRCm39) critical splice donor site probably null
R5746:Vmn2r11 UTSW 5 109,201,560 (GRCm39) missense probably benign 0.41
R5995:Vmn2r11 UTSW 5 109,194,921 (GRCm39) missense probably damaging 1.00
R6147:Vmn2r11 UTSW 5 109,202,700 (GRCm39) missense probably benign 0.04
R6220:Vmn2r11 UTSW 5 109,201,434 (GRCm39) missense probably benign 0.09
R6374:Vmn2r11 UTSW 5 109,201,679 (GRCm39) missense possibly damaging 0.65
R6491:Vmn2r11 UTSW 5 109,196,800 (GRCm39) missense possibly damaging 0.95
R6804:Vmn2r11 UTSW 5 109,201,350 (GRCm39) missense probably damaging 1.00
R6814:Vmn2r11 UTSW 5 109,194,976 (GRCm39) missense possibly damaging 0.81
R6872:Vmn2r11 UTSW 5 109,194,976 (GRCm39) missense possibly damaging 0.81
R7014:Vmn2r11 UTSW 5 109,201,289 (GRCm39) missense probably damaging 1.00
R7041:Vmn2r11 UTSW 5 109,202,816 (GRCm39) missense probably damaging 1.00
R7043:Vmn2r11 UTSW 5 109,200,098 (GRCm39) missense probably benign 0.00
R7050:Vmn2r11 UTSW 5 109,202,657 (GRCm39) missense probably benign 0.05
R7184:Vmn2r11 UTSW 5 109,201,281 (GRCm39) missense probably damaging 1.00
R7388:Vmn2r11 UTSW 5 109,202,742 (GRCm39) missense probably benign 0.05
R7477:Vmn2r11 UTSW 5 109,207,214 (GRCm39) missense possibly damaging 0.67
R7524:Vmn2r11 UTSW 5 109,201,848 (GRCm39) missense probably benign 0.01
R7715:Vmn2r11 UTSW 5 109,195,307 (GRCm39) missense probably damaging 0.99
R7869:Vmn2r11 UTSW 5 109,199,986 (GRCm39) missense probably damaging 1.00
R8094:Vmn2r11 UTSW 5 109,201,626 (GRCm39) missense probably damaging 1.00
R8277:Vmn2r11 UTSW 5 109,202,833 (GRCm39) missense probably benign 0.00
R8506:Vmn2r11 UTSW 5 109,207,270 (GRCm39) missense probably benign 0.00
R8676:Vmn2r11 UTSW 5 109,201,626 (GRCm39) missense probably damaging 1.00
R8701:Vmn2r11 UTSW 5 109,195,556 (GRCm39) missense probably damaging 1.00
R8749:Vmn2r11 UTSW 5 109,195,319 (GRCm39) missense probably damaging 0.97
R9046:Vmn2r11 UTSW 5 109,202,850 (GRCm39) missense probably benign 0.00
R9138:Vmn2r11 UTSW 5 109,201,904 (GRCm39) missense probably damaging 1.00
R9267:Vmn2r11 UTSW 5 109,199,929 (GRCm39) missense possibly damaging 0.93
R9306:Vmn2r11 UTSW 5 109,196,831 (GRCm39) missense probably damaging 1.00
R9384:Vmn2r11 UTSW 5 109,201,266 (GRCm39) missense probably damaging 1.00
R9443:Vmn2r11 UTSW 5 109,195,159 (GRCm39) nonsense probably null
R9520:Vmn2r11 UTSW 5 109,201,455 (GRCm39) missense probably benign 0.35
R9596:Vmn2r11 UTSW 5 109,201,563 (GRCm39) missense possibly damaging 0.67
R9677:Vmn2r11 UTSW 5 109,201,332 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- GCTTGAAAGCCATGAGCACAG -3'
(R):5'- TCTTTGCCAGCAGATATGGAAC -3'

Sequencing Primer
(F):5'- ACACTGTAGAAATAGCCACTGTG -3'
(R):5'- AACAGTGTGTGAGGTGTCCAG -3'
Posted On 2019-11-12