Incidental Mutation 'R7508:Vmn2r32'
ID 581893
Institutional Source Beutler Lab
Gene Symbol Vmn2r32
Ensembl Gene ENSMUSG00000096743
Gene Name vomeronasal 2, receptor 32
Synonyms V2r5
MMRRC Submission 045581-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.190) question?
Stock # R7508 (G1)
Quality Score 121.008
Status Not validated
Chromosome 7
Chromosomal Location 7463015-7479973 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 7467374 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Methionine at position 515 (V515M)
Ref Sequence ENSEMBL: ENSMUSP00000092462 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094866]
AlphaFold K7N686
Predicted Effect possibly damaging
Transcript: ENSMUST00000094866
AA Change: V515M

PolyPhen 2 Score 0.870 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000092462
Gene: ENSMUSG00000096743
AA Change: V515M

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 470 3.6e-33 PFAM
Pfam:NCD3G 512 565 8.1e-21 PFAM
Pfam:7tm_3 598 833 9.5e-55 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (56/56)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra3 C T 5: 50,016,867 (GRCm38) A110T probably benign Het
Adra1a A C 14: 66,637,935 (GRCm38) I120L probably damaging Het
Ahnak2 C T 12: 112,774,405 (GRCm38) V1078I possibly damaging Het
Ccser1 A G 6: 61,570,723 (GRCm38) H590R probably benign Het
Cdh12 T G 15: 21,583,765 (GRCm38) L564V probably benign Het
Celsr3 T A 9: 108,836,622 (GRCm38) H1900Q probably benign Het
Clasp1 T A 1: 118,545,434 (GRCm38) M918K probably benign Het
Cmtm6 A G 9: 114,731,240 (GRCm38) E2G probably damaging Het
Ctsg A G 14: 56,100,541 (GRCm38) probably null Het
Cylc2 T A 4: 51,229,256 (GRCm38) probably null Het
Dna2 A G 10: 62,971,993 (GRCm38) probably null Het
Dnaic1 G A 4: 41,614,323 (GRCm38) R333H probably benign Het
Egln3 T C 12: 54,180,628 (GRCm38) D239G probably benign Het
Fam13a A T 6: 58,987,284 (GRCm38) D54E probably damaging Het
Fn1 A G 1: 71,597,516 (GRCm38) V2159A probably benign Het
Gcnt2 T A 13: 40,887,681 (GRCm38) F105L probably benign Het
Gm5788 T C 12: 87,494,842 (GRCm38) M41T possibly damaging Het
Gpd1 G A 15: 99,722,086 (GRCm38) S255N probably damaging Het
Hacd4 A G 4: 88,437,478 (GRCm38) F57L probably benign Het
Helb T C 10: 120,105,283 (GRCm38) D500G probably benign Het
Ighv1-26 G A 12: 114,788,442 (GRCm38) S94F probably damaging Het
Kirrel T C 3: 87,083,439 (GRCm38) D692G possibly damaging Het
Klra7 A T 6: 130,230,091 (GRCm38) probably null Het
Lyl1 T C 8: 84,704,300 (GRCm38) V277A probably benign Het
Mon2 A C 10: 123,023,939 (GRCm38) W811G probably damaging Het
Myo9b T C 8: 71,354,801 (GRCm38) L1627P probably benign Het
Neurl1b C G 17: 26,438,746 (GRCm38) H219Q probably benign Het
Odf4 A T 11: 68,922,423 (GRCm38) C218S possibly damaging Het
Olfr1038-ps A G 2: 86,121,938 (GRCm38) N5S possibly damaging Het
Olfr11 T A 13: 21,638,609 (GRCm38) I305F probably benign Het
Pde5a A G 3: 122,818,030 (GRCm38) D571G probably damaging Het
Pgc A G 17: 47,734,186 (GRCm38) E343G probably benign Het
Pik3cd A G 4: 149,654,583 (GRCm38) F667L possibly damaging Het
Prf1 G A 10: 61,300,155 (GRCm38) R70H possibly damaging Het
Ptprb C T 10: 116,353,991 (GRCm38) Q1565* probably null Het
Rapgef4 T A 2: 72,205,733 (GRCm38) N523K probably benign Het
Rbm25 T C 12: 83,672,877 (GRCm38) L557P probably damaging Het
Rhobtb3 C T 13: 75,878,857 (GRCm38) V466I probably benign Het
Rnpep A G 1: 135,278,858 (GRCm38) V166A probably benign Het
Sgo2a A G 1: 58,017,795 (GRCm38) K1046R probably benign Het
Slc12a2 T C 18: 57,904,393 (GRCm38) V525A probably benign Het
Slc1a4 A T 11: 20,306,487 (GRCm38) I448N probably damaging Het
Slc29a4 C T 5: 142,718,506 (GRCm38) P305L probably benign Het
Slc9a5 T A 8: 105,363,253 (GRCm38) probably null Het
Spag16 A T 1: 69,887,520 (GRCm38) N258I possibly damaging Het
Sspo T A 6: 48,466,699 (GRCm38) L2076Q probably damaging Het
Taok1 T A 11: 77,545,326 (GRCm38) H704L probably damaging Het
Tbc1d9b T C 11: 50,145,120 (GRCm38) F148L probably damaging Het
Tm4sf1 A G 3: 57,294,755 (GRCm38) Y12H probably benign Het
Traj6 C T 14: 54,212,714 (GRCm38) T9M Het
Ttll4 A G 1: 74,687,259 (GRCm38) N672S possibly damaging Het
Ube3a T A 7: 59,303,689 (GRCm38) H790Q possibly damaging Het
Usp49 G A 17: 47,672,280 (GRCm38) R70Q probably benign Het
Wars A G 12: 108,882,875 (GRCm38) S49P probably benign Het
Zbp1 T A 2: 173,207,811 (GRCm38) Q386L possibly damaging Het
Zfp369 T C 13: 65,279,273 (GRCm38) F10S unknown Het
Zfp512 C G 5: 31,473,539 (GRCm38) I408M possibly damaging Het
Zfp952 A G 17: 33,003,782 (GRCm38) I412V probably benign Het
Other mutations in Vmn2r32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02140:Vmn2r32 APN 7 7,476,697 (GRCm38) missense probably damaging 0.97
IGL02333:Vmn2r32 APN 7 7,464,144 (GRCm38) missense probably damaging 1.00
IGL02406:Vmn2r32 APN 7 7,476,710 (GRCm38) missense probably benign
IGL02428:Vmn2r32 APN 7 7,474,284 (GRCm38) missense probably benign 0.02
IGL02484:Vmn2r32 APN 7 7,464,117 (GRCm38) missense probably damaging 1.00
IGL03277:Vmn2r32 APN 7 7,474,252 (GRCm38) missense probably benign 0.23
IGL03366:Vmn2r32 APN 7 7,464,030 (GRCm38) missense probably damaging 0.99
R1055:Vmn2r32 UTSW 7 7,474,327 (GRCm38) nonsense probably null
R1695:Vmn2r32 UTSW 7 7,463,992 (GRCm38) missense probably benign 0.01
R2172:Vmn2r32 UTSW 7 7,474,615 (GRCm38) missense probably damaging 0.99
R2262:Vmn2r32 UTSW 7 7,474,619 (GRCm38) missense probably benign
R3150:Vmn2r32 UTSW 7 7,472,555 (GRCm38) missense probably benign
R4362:Vmn2r32 UTSW 7 7,479,858 (GRCm38) nonsense probably null
R4432:Vmn2r32 UTSW 7 7,479,919 (GRCm38) missense probably damaging 0.98
R4851:Vmn2r32 UTSW 7 7,479,954 (GRCm38) missense possibly damaging 0.59
R4949:Vmn2r32 UTSW 7 7,464,084 (GRCm38) missense probably benign 0.22
R5990:Vmn2r32 UTSW 7 7,479,810 (GRCm38) missense probably damaging 0.97
R6083:Vmn2r32 UTSW 7 7,464,210 (GRCm38) missense probably benign 0.15
R6084:Vmn2r32 UTSW 7 7,464,210 (GRCm38) missense probably benign 0.15
R6116:Vmn2r32 UTSW 7 7,464,093 (GRCm38) missense probably damaging 1.00
R6263:Vmn2r32 UTSW 7 7,476,692 (GRCm38) missense possibly damaging 0.90
R6889:Vmn2r32 UTSW 7 7,472,574 (GRCm38) missense possibly damaging 0.82
R7286:Vmn2r32 UTSW 7 7,479,808 (GRCm38) missense probably benign 0.21
R7390:Vmn2r32 UTSW 7 7,479,852 (GRCm38) missense probably benign 0.00
R7412:Vmn2r32 UTSW 7 7,474,213 (GRCm38) missense possibly damaging 0.53
R8812:Vmn2r32 UTSW 7 7,474,670 (GRCm38) missense probably damaging 1.00
R8968:Vmn2r32 UTSW 7 7,474,205 (GRCm38) missense probably benign 0.00
R9331:Vmn2r32 UTSW 7 7,464,403 (GRCm38) nonsense probably null
R9358:Vmn2r32 UTSW 7 7,474,198 (GRCm38) missense probably damaging 1.00
Z1177:Vmn2r32 UTSW 7 7,474,161 (GRCm38) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TGACTTCATTATTCCAGGGTGATG -3'
(R):5'- ACCAGGTTGCAACTTCTGTAG -3'

Sequencing Primer
(F):5'- TGGAAGAGAAATACATATCTTCGGG -3'
(R):5'- TAATCCCAGCACTTTGGAGG -3'
Posted On 2019-10-17