Incidental Mutation 'R6116:Vmn2r32'
ID 485117
Institutional Source Beutler Lab
Gene Symbol Vmn2r32
Ensembl Gene ENSMUSG00000096743
Gene Name vomeronasal 2, receptor 32
Synonyms V2r5
MMRRC Submission 044265-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.249) question?
Stock # R6116 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 7466968-7482972 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 7467092 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 812 (I812N)
Ref Sequence ENSEMBL: ENSMUSP00000092462 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094866]
AlphaFold K7N686
Predicted Effect probably damaging
Transcript: ENSMUST00000094866
AA Change: I812N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000092462
Gene: ENSMUSG00000096743
AA Change: I812N

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: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahnak T A 19: 8,990,327 (GRCm39) probably benign Het
Apc A T 18: 34,449,508 (GRCm39) I2101F probably damaging Het
Bpifa3 G A 2: 153,975,633 (GRCm39) V68I possibly damaging Het
Csmd1 T A 8: 16,261,864 (GRCm39) I878F probably damaging Het
Cyp2c67 A T 19: 39,605,879 (GRCm39) M339K probably damaging Het
Dock3 A G 9: 106,809,161 (GRCm39) Y1321H probably damaging Het
Dsc1 G T 18: 20,230,356 (GRCm39) D316E probably benign Het
Eno3 C T 11: 70,552,401 (GRCm39) T351M possibly damaging Het
Erbb2 T A 11: 98,318,225 (GRCm39) F487Y probably damaging Het
Exosc10 T C 4: 148,657,810 (GRCm39) L652P probably benign Het
Glmn A T 5: 107,705,206 (GRCm39) M470K probably damaging Het
Gm15446 T A 5: 110,090,902 (GRCm39) C385S probably damaging Het
Hspa8 A G 9: 40,716,271 (GRCm39) E581G probably damaging Het
Igfn1 T C 1: 135,898,205 (GRCm39) D787G probably benign Het
Igkv12-44 T C 6: 69,791,838 (GRCm39) T42A possibly damaging Het
Itsn2 T C 12: 4,679,939 (GRCm39) probably benign Het
Jade2 T C 11: 51,726,460 (GRCm39) E84G probably damaging Het
Lpar3 T A 3: 145,946,352 (GRCm39) M10K possibly damaging Het
Lpin2 A G 17: 71,550,925 (GRCm39) D695G probably damaging Het
Mosmo T A 7: 120,325,418 (GRCm39) L7H probably damaging Het
Ms4a8a C T 19: 11,058,436 (GRCm39) A9T unknown Het
Myb T C 10: 21,030,653 (GRCm39) D48G probably damaging Het
Neurod6 T C 6: 55,655,776 (GRCm39) Y287C probably damaging Het
Olr1 T A 6: 129,476,947 (GRCm39) D106V probably damaging Het
Or11a4 A G 17: 37,536,459 (GRCm39) T148A probably benign Het
Or8b4 A G 9: 37,829,955 (GRCm39) M1V probably null Het
Peg10 C CCCATCAGGA 6: 4,756,351 (GRCm39) probably benign Het
Plch1 C T 3: 63,609,444 (GRCm39) R912H probably damaging Het
Ppfia3 T C 7: 45,004,127 (GRCm39) Y505C probably damaging Het
Sdk2 T A 11: 113,745,190 (GRCm39) I702F probably damaging Het
Slc16a11 T C 11: 70,106,262 (GRCm39) F119L probably benign Het
Slc2a10 A C 2: 165,359,623 (GRCm39) T496P probably damaging Het
Slc7a2 T C 8: 41,353,206 (GRCm39) Y181H probably damaging Het
Spata31e5 G A 1: 28,817,780 (GRCm39) A84V probably benign Het
Stab2 G T 10: 86,743,054 (GRCm39) P1185Q probably damaging Het
Tcf7l2 T A 19: 55,907,446 (GRCm39) S335R probably damaging Het
Ttc41 G A 10: 86,594,952 (GRCm39) probably null Het
Wdr24 C T 17: 26,043,579 (GRCm39) H134Y probably benign Het
Other mutations in Vmn2r32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02140:Vmn2r32 APN 7 7,479,696 (GRCm39) missense probably damaging 0.97
IGL02333:Vmn2r32 APN 7 7,467,143 (GRCm39) missense probably damaging 1.00
IGL02406:Vmn2r32 APN 7 7,479,709 (GRCm39) missense probably benign
IGL02428:Vmn2r32 APN 7 7,477,283 (GRCm39) missense probably benign 0.02
IGL02484:Vmn2r32 APN 7 7,467,116 (GRCm39) missense probably damaging 1.00
IGL03277:Vmn2r32 APN 7 7,477,251 (GRCm39) missense probably benign 0.23
IGL03366:Vmn2r32 APN 7 7,467,029 (GRCm39) missense probably damaging 0.99
R1055:Vmn2r32 UTSW 7 7,477,326 (GRCm39) nonsense probably null
R1695:Vmn2r32 UTSW 7 7,466,991 (GRCm39) missense probably benign 0.01
R2172:Vmn2r32 UTSW 7 7,477,614 (GRCm39) missense probably damaging 0.99
R2262:Vmn2r32 UTSW 7 7,477,618 (GRCm39) missense probably benign
R3150:Vmn2r32 UTSW 7 7,475,554 (GRCm39) missense probably benign
R4362:Vmn2r32 UTSW 7 7,482,857 (GRCm39) nonsense probably null
R4432:Vmn2r32 UTSW 7 7,482,918 (GRCm39) missense probably damaging 0.98
R4851:Vmn2r32 UTSW 7 7,482,953 (GRCm39) missense possibly damaging 0.59
R4949:Vmn2r32 UTSW 7 7,467,083 (GRCm39) missense probably benign 0.22
R5990:Vmn2r32 UTSW 7 7,482,809 (GRCm39) missense probably damaging 0.97
R6083:Vmn2r32 UTSW 7 7,467,209 (GRCm39) missense probably benign 0.15
R6084:Vmn2r32 UTSW 7 7,467,209 (GRCm39) missense probably benign 0.15
R6263:Vmn2r32 UTSW 7 7,479,691 (GRCm39) missense possibly damaging 0.90
R6889:Vmn2r32 UTSW 7 7,475,573 (GRCm39) missense possibly damaging 0.82
R7286:Vmn2r32 UTSW 7 7,482,807 (GRCm39) missense probably benign 0.21
R7390:Vmn2r32 UTSW 7 7,482,851 (GRCm39) missense probably benign 0.00
R7412:Vmn2r32 UTSW 7 7,477,212 (GRCm39) missense possibly damaging 0.53
R7508:Vmn2r32 UTSW 7 7,470,373 (GRCm39) missense possibly damaging 0.87
R8812:Vmn2r32 UTSW 7 7,477,669 (GRCm39) missense probably damaging 1.00
R8968:Vmn2r32 UTSW 7 7,477,204 (GRCm39) missense probably benign 0.00
R9331:Vmn2r32 UTSW 7 7,467,402 (GRCm39) nonsense probably null
R9358:Vmn2r32 UTSW 7 7,477,197 (GRCm39) missense probably damaging 1.00
Z1177:Vmn2r32 UTSW 7 7,477,160 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TAGAGCAACCAGTGAGAGTGATTC -3'
(R):5'- GTCCTTGGATACTTGGCCTG -3'

Sequencing Primer
(F):5'- CAACCAGTGAGAGTGATTCTAAAAC -3'
(R):5'- GATACTTGGCCTGCCTGG -3'
Posted On 2017-08-16