Incidental Mutation 'R5016:Vmn2r91'
ID 385598
Institutional Source Beutler Lab
Gene Symbol Vmn2r91
Ensembl Gene ENSMUSG00000091206
Gene Name vomeronasal 2, receptor 91
Synonyms EG665210
MMRRC Submission 042607-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R5016 (G1)
Quality Score 216
Status Validated
Chromosome 17
Chromosomal Location 18305319-18356905 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 18330322 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 535 (Y535*)
Ref Sequence ENSEMBL: ENSMUSP00000127465 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172359]
AlphaFold E9Q2U5
Predicted Effect probably null
Transcript: ENSMUST00000172359
AA Change: Y535*
SMART Domains Protein: ENSMUSP00000127465
Gene: ENSMUSG00000091206
AA Change: Y535*

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:ANF_receptor 83 462 2.2e-38 PFAM
Pfam:NCD3G 510 564 6.7e-20 PFAM
Pfam:7tm_3 597 832 2.1e-53 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 98.3%
  • 3x: 97.2%
  • 10x: 95.1%
  • 20x: 91.0%
Validation Efficiency 97% (56/58)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi3bp C T 16: 56,491,631 (GRCm39) P768S probably damaging Het
Adprhl1 A G 8: 13,274,889 (GRCm39) L623P possibly damaging Het
Anapc1 A T 2: 128,449,095 (GRCm39) probably benign Het
Ankzf1 C A 1: 75,172,622 (GRCm39) probably benign Het
Ash1l A G 3: 88,889,630 (GRCm39) D503G probably damaging Het
Atp7b T C 8: 22,505,885 (GRCm39) probably null Het
Bach1 T A 16: 87,516,206 (GRCm39) V249D possibly damaging Het
Ccdc158 A G 5: 92,805,751 (GRCm39) S335P probably benign Het
Chd9 T A 8: 91,733,254 (GRCm39) C1374* probably null Het
Col16a1 C T 4: 129,972,988 (GRCm39) T643M probably benign Het
Cygb A G 11: 116,540,840 (GRCm39) F49L probably benign Het
Dnah17 G C 11: 117,971,592 (GRCm39) T2147S probably damaging Het
Drd3 C A 16: 43,582,609 (GRCm39) A34E possibly damaging Het
Ephb6 G A 6: 41,595,041 (GRCm39) R685Q probably benign Het
Ezh1 G A 11: 101,090,063 (GRCm39) probably benign Het
Gpr19 T A 6: 134,846,880 (GRCm39) K231* probably null Het
Gpr61 A G 3: 108,057,983 (GRCm39) V226A possibly damaging Het
Gprc5c G T 11: 114,755,093 (GRCm39) V257L possibly damaging Het
Hnrnpul2 A G 19: 8,800,189 (GRCm39) K185R possibly damaging Het
Igsf9 A C 1: 172,318,279 (GRCm39) T140P probably damaging Het
Ksr2 A G 5: 117,638,857 (GRCm39) D87G probably benign Het
Llgl2 A G 11: 115,744,250 (GRCm39) E843G probably damaging Het
Ltbp4 GT G 7: 27,027,110 (GRCm39) probably null Het
Luc7l2 A G 6: 38,562,036 (GRCm39) I20V possibly damaging Het
Mcm6 G A 1: 128,271,164 (GRCm39) T485M probably damaging Het
Miox A G 15: 89,219,767 (GRCm39) D85G probably null Het
Nudt18 T C 14: 70,816,903 (GRCm39) F169S probably benign Het
Nxpe4 A G 9: 48,304,185 (GRCm39) N91D probably benign Het
Or13c7 T C 4: 43,854,596 (GRCm39) S96P probably benign Het
Or6c215 A G 10: 129,637,662 (GRCm39) V244A probably benign Het
Or8k39 T G 2: 86,563,090 (GRCm39) I289L probably benign Het
Pdss2 G T 10: 43,098,001 (GRCm39) A82S probably damaging Het
Ptprs T C 17: 56,726,070 (GRCm39) D998G probably damaging Het
Rasd2 C A 8: 75,948,603 (GRCm39) N176K probably damaging Het
Serpinb3a A G 1: 106,974,060 (GRCm39) F284L probably damaging Het
Skint6 T A 4: 113,028,730 (GRCm39) probably null Het
Slc12a6 C T 2: 112,186,972 (GRCm39) probably benign Het
Slc22a19 G A 19: 7,651,737 (GRCm39) T490M probably benign Het
Sp2 A T 11: 96,846,658 (GRCm39) C562S probably damaging Het
Specc1 A G 11: 62,009,783 (GRCm39) E433G possibly damaging Het
Sspo C T 6: 48,429,214 (GRCm39) Q451* probably null Het
St6galnac1 A T 11: 116,656,706 (GRCm39) S478T probably damaging Het
Steap4 C T 5: 8,026,699 (GRCm39) R221* probably null Het
Ugt1a5 C G 1: 88,093,963 (GRCm39) R64G probably benign Het
Vmn1r202 A T 13: 22,686,375 (GRCm39) F14Y probably damaging Het
Vmn2r79 T C 7: 86,686,548 (GRCm39) V643A probably benign Het
Wdr3 A T 3: 100,048,936 (GRCm39) probably benign Het
Wdr95 T C 5: 149,468,266 (GRCm39) M41T probably benign Het
Other mutations in Vmn2r91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00983:Vmn2r91 APN 17 18,325,820 (GRCm39) missense probably benign 0.00
IGL01121:Vmn2r91 APN 17 18,356,766 (GRCm39) missense possibly damaging 0.94
IGL01464:Vmn2r91 APN 17 18,327,864 (GRCm39) missense probably null 0.00
IGL02003:Vmn2r91 APN 17 18,327,921 (GRCm39) missense probably benign
IGL02709:Vmn2r91 APN 17 18,325,711 (GRCm39) missense possibly damaging 0.74
IGL02795:Vmn2r91 APN 17 18,305,539 (GRCm39) missense probably benign 0.01
IGL02813:Vmn2r91 APN 17 18,356,348 (GRCm39) missense possibly damaging 0.91
IGL02830:Vmn2r91 APN 17 18,356,884 (GRCm39) missense probably benign 0.01
IGL03130:Vmn2r91 APN 17 18,330,373 (GRCm39) splice site probably benign
BB006:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
BB016:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R0164:Vmn2r91 UTSW 17 18,326,399 (GRCm39) missense probably benign 0.00
R0164:Vmn2r91 UTSW 17 18,326,399 (GRCm39) missense probably benign 0.00
R0393:Vmn2r91 UTSW 17 18,325,712 (GRCm39) missense probably damaging 1.00
R1142:Vmn2r91 UTSW 17 18,356,705 (GRCm39) missense probably damaging 1.00
R1603:Vmn2r91 UTSW 17 18,326,405 (GRCm39) missense probably benign 0.04
R1992:Vmn2r91 UTSW 17 18,356,142 (GRCm39) missense probably damaging 1.00
R2182:Vmn2r91 UTSW 17 18,325,691 (GRCm39) missense possibly damaging 0.94
R2424:Vmn2r91 UTSW 17 18,356,431 (GRCm39) nonsense probably null
R2512:Vmn2r91 UTSW 17 18,356,048 (GRCm39) missense probably benign
R2885:Vmn2r91 UTSW 17 18,325,628 (GRCm39) missense probably benign 0.00
R2909:Vmn2r91 UTSW 17 18,356,661 (GRCm39) missense probably damaging 1.00
R3009:Vmn2r91 UTSW 17 18,325,717 (GRCm39) missense probably benign 0.11
R3079:Vmn2r91 UTSW 17 18,355,973 (GRCm39) splice site probably null
R3080:Vmn2r91 UTSW 17 18,355,973 (GRCm39) splice site probably null
R3434:Vmn2r91 UTSW 17 18,330,370 (GRCm39) splice site probably benign
R3723:Vmn2r91 UTSW 17 18,305,540 (GRCm39) critical splice donor site probably null
R3829:Vmn2r91 UTSW 17 18,325,759 (GRCm39) missense probably damaging 1.00
R3845:Vmn2r91 UTSW 17 18,327,860 (GRCm39) missense probably benign 0.00
R3846:Vmn2r91 UTSW 17 18,327,860 (GRCm39) missense probably benign 0.00
R4118:Vmn2r91 UTSW 17 18,330,358 (GRCm39) missense probably damaging 1.00
R4285:Vmn2r91 UTSW 17 18,356,030 (GRCm39) missense probably benign 0.00
R4729:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R4793:Vmn2r91 UTSW 17 18,325,658 (GRCm39) missense probably damaging 1.00
R4932:Vmn2r91 UTSW 17 18,356,751 (GRCm39) missense possibly damaging 0.84
R5018:Vmn2r91 UTSW 17 18,356,700 (GRCm39) missense probably damaging 1.00
R5605:Vmn2r91 UTSW 17 18,356,763 (GRCm39) missense probably damaging 1.00
R5815:Vmn2r91 UTSW 17 18,326,464 (GRCm39) missense probably benign 0.01
R6146:Vmn2r91 UTSW 17 18,356,518 (GRCm39) missense probably benign 0.07
R6187:Vmn2r91 UTSW 17 18,326,888 (GRCm39) missense probably benign 0.05
R6426:Vmn2r91 UTSW 17 18,355,865 (GRCm39) splice site probably null
R6450:Vmn2r91 UTSW 17 18,305,527 (GRCm39) missense probably damaging 0.98
R6767:Vmn2r91 UTSW 17 18,327,807 (GRCm39) missense probably damaging 0.98
R6986:Vmn2r91 UTSW 17 18,356,271 (GRCm39) missense probably benign 0.10
R7112:Vmn2r91 UTSW 17 18,325,880 (GRCm39) missense possibly damaging 0.83
R7178:Vmn2r91 UTSW 17 18,356,424 (GRCm39) missense probably damaging 1.00
R7330:Vmn2r91 UTSW 17 18,326,429 (GRCm39) missense probably damaging 1.00
R7368:Vmn2r91 UTSW 17 18,356,540 (GRCm39) missense possibly damaging 0.75
R7380:Vmn2r91 UTSW 17 18,356,838 (GRCm39) nonsense probably null
R7397:Vmn2r91 UTSW 17 18,356,060 (GRCm39) missense probably benign 0.02
R7625:Vmn2r91 UTSW 17 18,325,693 (GRCm39) missense probably damaging 1.00
R7739:Vmn2r91 UTSW 17 18,356,080 (GRCm39) missense probably benign 0.00
R7749:Vmn2r91 UTSW 17 18,356,540 (GRCm39) missense possibly damaging 0.75
R7755:Vmn2r91 UTSW 17 18,330,311 (GRCm39) missense possibly damaging 0.88
R7929:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R7981:Vmn2r91 UTSW 17 18,327,887 (GRCm39) missense probably benign 0.02
R8211:Vmn2r91 UTSW 17 18,326,762 (GRCm39) missense probably damaging 1.00
R8325:Vmn2r91 UTSW 17 18,356,625 (GRCm39) missense probably damaging 1.00
R8781:Vmn2r91 UTSW 17 18,305,323 (GRCm39) missense possibly damaging 0.78
R8974:Vmn2r91 UTSW 17 18,325,636 (GRCm39) missense probably benign 0.27
R9047:Vmn2r91 UTSW 17 18,326,296 (GRCm39) missense probably benign 0.00
R9048:Vmn2r91 UTSW 17 18,356,122 (GRCm39) missense probably benign 0.00
R9109:Vmn2r91 UTSW 17 18,327,905 (GRCm39) missense probably damaging 1.00
R9211:Vmn2r91 UTSW 17 18,356,819 (GRCm39) nonsense probably null
R9555:Vmn2r91 UTSW 17 18,325,792 (GRCm39) missense possibly damaging 0.78
R9616:Vmn2r91 UTSW 17 18,356,305 (GRCm39) missense possibly damaging 0.81
Predicted Primers PCR Primer
(F):5'- GTCTAGGTGTTAACAACAGTACTTTGC -3'
(R):5'- TGGCACTGTCCAATGTAAAGC -3'

Sequencing Primer
(F):5'- ACAACAGTACTTTGCTTTTCAGTG -3'
(R):5'- AGCTATTTCAAGGGGATGATGATG -3'
Posted On 2016-05-10