Incidental Mutation 'R9795:Vmn2r97'
ID 734907
Institutional Source Beutler Lab
Gene Symbol Vmn2r97
Ensembl Gene ENSMUSG00000091491
Gene Name vomeronasal 2, receptor 97
Synonyms EG627367
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R9795 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 19134584-19168333 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 19167561 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 605 (V605D)
Ref Sequence ENSEMBL: ENSMUSP00000129313 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168710] [ENSMUST00000232219]
AlphaFold K7N6Z2
Predicted Effect probably damaging
Transcript: ENSMUST00000168710
AA Change: V605D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129313
Gene: ENSMUSG00000091491
AA Change: V605D

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 82 442 2.9e-36 PFAM
Pfam:NCD3G 513 566 4.9e-21 PFAM
Pfam:7tm_3 599 834 1.7e-52 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000232219
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.4%
  • 20x: 98.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts20 C T 15: 94,301,180 (GRCm39) G115R possibly damaging Het
Adgrl3 T C 5: 81,837,421 (GRCm39) V701A probably damaging Het
Afap1l1 T C 18: 61,874,822 (GRCm39) D453G possibly damaging Het
Ano1 A T 7: 144,175,434 (GRCm39) W495R probably damaging Het
Apc T A 18: 34,447,628 (GRCm39) L1508Q probably damaging Het
Bbs12 C T 3: 37,374,224 (GRCm39) T224I possibly damaging Het
Cald1 A T 6: 34,723,071 (GRCm39) M52L Het
Calhm6 T C 10: 34,002,544 (GRCm39) I180V probably damaging Het
Ccdc9b T C 2: 118,587,784 (GRCm39) S517G unknown Het
Cdk12 T A 11: 98,102,051 (GRCm39) D636E unknown Het
Cfap53 A G 18: 74,438,741 (GRCm39) D306G probably benign Het
Cntnap4 T C 8: 113,608,357 (GRCm39) V1259A probably benign Het
Cntnap5c A T 17: 58,409,192 (GRCm39) T477S probably benign Het
Epha3 T C 16: 63,372,910 (GRCm39) E931G probably benign Het
Foxred1 CGGG CGG 9: 35,122,152 (GRCm39) probably null Het
Gstt1 T C 10: 75,634,391 (GRCm39) probably benign Het
Hao1 T A 2: 134,372,552 (GRCm39) Y152F possibly damaging Het
Hcn4 C T 9: 58,760,762 (GRCm39) Q436* probably null Het
Hmcn1 G A 1: 150,608,689 (GRCm39) P1498S possibly damaging Het
Igkv4-79 A G 6: 69,020,169 (GRCm39) S49P probably damaging Het
Krt73 C A 15: 101,710,725 (GRCm39) R3L probably damaging Het
Lrriq3 T C 3: 154,893,313 (GRCm39) M338T probably benign Het
Ltbp2 A T 12: 84,876,128 (GRCm39) I493N probably damaging Het
Ly6e G T 15: 74,830,390 (GRCm39) C80F probably damaging Het
Map1a T C 2: 121,121,304 (GRCm39) probably null Het
Mitf A G 6: 97,970,143 (GRCm39) H137R probably benign Het
Nr1h4 T G 10: 89,314,651 (GRCm39) T286P probably benign Het
Nsd2 A G 5: 34,003,489 (GRCm39) D213G possibly damaging Het
Nuggc T C 14: 65,847,345 (GRCm39) S131P probably damaging Het
Nwd2 A G 5: 63,964,232 (GRCm39) E1272G probably damaging Het
Or2y1 A T 11: 49,385,882 (GRCm39) N174I probably damaging Het
Or4a78 T C 2: 89,497,811 (GRCm39) I140V probably benign Het
Or4f14c T C 2: 111,941,330 (GRCm39) H89R probably benign Het
Or5ac17 T A 16: 59,036,938 (GRCm39) I13F possibly damaging Het
Or5p79 A G 7: 108,221,869 (GRCm39) I283M probably benign Het
Or7e170 T A 9: 19,795,347 (GRCm39) M85L probably benign Het
Or7g32 T C 9: 19,408,412 (GRCm39) Y123H probably damaging Het
Or8h9 T A 2: 86,789,119 (GRCm39) I228F probably damaging Het
Pacsin3 C A 2: 91,094,160 (GRCm39) A363D probably benign Het
Pcdh17 C T 14: 84,770,350 (GRCm39) R943* probably null Het
Pkhd1l1 T C 15: 44,406,983 (GRCm39) S2407P probably benign Het
Ppip5k2 A T 1: 97,671,822 (GRCm39) Y489* probably null Het
Qrich1 T A 9: 108,411,089 (GRCm39) S205T probably benign Het
Rasgrp1 T C 2: 117,118,429 (GRCm39) D520G probably benign Het
Rbm20 C A 19: 53,852,551 (GRCm39) T1177K probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Sel1l3 C A 5: 53,329,924 (GRCm39) R477L probably benign Het
Slc27a3 C T 3: 90,296,875 (GRCm39) W32* probably null Het
Slc5a8 T C 10: 88,757,591 (GRCm39) I527T possibly damaging Het
Slc6a7 C A 18: 61,138,866 (GRCm39) R214L probably benign Het
Stx7 T C 10: 24,057,475 (GRCm39) L167P probably damaging Het
Sult1d1 T A 5: 87,712,655 (GRCm39) N63I probably damaging Het
Ttc23l T A 15: 10,537,731 (GRCm39) I180F probably benign Het
Usp31 A G 7: 121,247,499 (GRCm39) S1315P probably benign Het
Usp9y T C Y: 1,364,679 (GRCm39) M1045V probably benign Het
Vmn2r118 T C 17: 55,899,496 (GRCm39) T803A probably damaging Het
Wdr26 A G 1: 181,036,812 (GRCm39) F143S probably damaging Het
Zfp51 T G 17: 21,682,051 (GRCm39) probably null Het
Other mutations in Vmn2r97
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00897:Vmn2r97 APN 17 19,167,921 (GRCm39) missense probably benign 0.37
IGL00962:Vmn2r97 APN 17 19,149,490 (GRCm39) missense probably damaging 1.00
IGL01704:Vmn2r97 APN 17 19,168,073 (GRCm39) missense probably damaging 0.99
IGL01888:Vmn2r97 APN 17 19,149,286 (GRCm39) nonsense probably null
IGL02429:Vmn2r97 APN 17 19,150,596 (GRCm39) missense possibly damaging 0.94
IGL02742:Vmn2r97 APN 17 19,149,432 (GRCm39) missense probably damaging 0.97
IGL02934:Vmn2r97 APN 17 19,149,947 (GRCm39) missense probably benign 0.00
IGL02978:Vmn2r97 APN 17 19,168,298 (GRCm39) missense probably benign 0.01
IGL03230:Vmn2r97 APN 17 19,149,668 (GRCm39) missense probably benign 0.10
IGL03241:Vmn2r97 APN 17 19,148,438 (GRCm39) missense probably benign 0.11
IGL03050:Vmn2r97 UTSW 17 19,167,900 (GRCm39) missense possibly damaging 0.84
PIT4469001:Vmn2r97 UTSW 17 19,149,878 (GRCm39) missense probably benign 0.00
R0482:Vmn2r97 UTSW 17 19,167,930 (GRCm39) missense probably damaging 1.00
R0514:Vmn2r97 UTSW 17 19,134,734 (GRCm39) missense probably benign 0.25
R0944:Vmn2r97 UTSW 17 19,167,665 (GRCm39) missense probably benign 0.13
R1061:Vmn2r97 UTSW 17 19,148,440 (GRCm39) nonsense probably null
R1546:Vmn2r97 UTSW 17 19,168,110 (GRCm39) missense probably damaging 1.00
R1725:Vmn2r97 UTSW 17 19,149,397 (GRCm39) missense probably benign 0.43
R1860:Vmn2r97 UTSW 17 19,167,648 (GRCm39) missense probably benign 0.01
R1938:Vmn2r97 UTSW 17 19,149,593 (GRCm39) missense probably benign 0.01
R1944:Vmn2r97 UTSW 17 19,160,500 (GRCm39) missense probably benign 0.00
R2027:Vmn2r97 UTSW 17 19,149,944 (GRCm39) missense unknown
R2106:Vmn2r97 UTSW 17 19,168,100 (GRCm39) missense probably damaging 1.00
R2151:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2153:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2154:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2516:Vmn2r97 UTSW 17 19,167,814 (GRCm39) missense probably benign
R3739:Vmn2r97 UTSW 17 19,148,413 (GRCm39) missense probably damaging 1.00
R3744:Vmn2r97 UTSW 17 19,149,890 (GRCm39) missense probably benign
R3885:Vmn2r97 UTSW 17 19,148,596 (GRCm39) missense possibly damaging 0.90
R3899:Vmn2r97 UTSW 17 19,167,873 (GRCm39) missense probably damaging 0.96
R4115:Vmn2r97 UTSW 17 19,148,332 (GRCm39) missense probably benign 0.01
R4247:Vmn2r97 UTSW 17 19,167,542 (GRCm39) missense possibly damaging 0.83
R4287:Vmn2r97 UTSW 17 19,168,337 (GRCm39) intron probably benign
R4439:Vmn2r97 UTSW 17 19,150,616 (GRCm39) missense probably benign 0.00
R4523:Vmn2r97 UTSW 17 19,149,333 (GRCm39) missense probably benign 0.03
R4783:Vmn2r97 UTSW 17 19,149,550 (GRCm39) missense probably benign
R4948:Vmn2r97 UTSW 17 19,167,561 (GRCm39) missense possibly damaging 0.95
R4981:Vmn2r97 UTSW 17 19,160,436 (GRCm39) nonsense probably null
R5029:Vmn2r97 UTSW 17 19,168,173 (GRCm39) missense probably damaging 1.00
R5200:Vmn2r97 UTSW 17 19,148,615 (GRCm39) missense probably damaging 1.00
R5541:Vmn2r97 UTSW 17 19,148,617 (GRCm39) nonsense probably null
R5637:Vmn2r97 UTSW 17 19,167,628 (GRCm39) nonsense probably null
R5765:Vmn2r97 UTSW 17 19,167,442 (GRCm39) nonsense probably null
R5885:Vmn2r97 UTSW 17 19,168,035 (GRCm39) missense possibly damaging 0.50
R6272:Vmn2r97 UTSW 17 19,167,861 (GRCm39) missense possibly damaging 0.70
R6553:Vmn2r97 UTSW 17 19,150,566 (GRCm39) nonsense probably null
R6818:Vmn2r97 UTSW 17 19,168,193 (GRCm39) missense possibly damaging 0.95
R6880:Vmn2r97 UTSW 17 19,134,770 (GRCm39) missense probably benign 0.00
R7012:Vmn2r97 UTSW 17 19,167,756 (GRCm39) missense probably damaging 0.99
R7023:Vmn2r97 UTSW 17 19,134,663 (GRCm39) missense probably damaging 1.00
R7044:Vmn2r97 UTSW 17 19,134,629 (GRCm39) missense probably benign 0.05
R7191:Vmn2r97 UTSW 17 19,150,548 (GRCm39) missense probably damaging 1.00
R7503:Vmn2r97 UTSW 17 19,148,470 (GRCm39) missense probably benign
R7862:Vmn2r97 UTSW 17 19,167,416 (GRCm39) missense probably damaging 1.00
R7876:Vmn2r97 UTSW 17 19,149,326 (GRCm39) missense probably damaging 0.97
R7890:Vmn2r97 UTSW 17 19,149,802 (GRCm39) missense probably benign 0.00
R7936:Vmn2r97 UTSW 17 19,150,662 (GRCm39) missense probably damaging 1.00
R7978:Vmn2r97 UTSW 17 19,167,854 (GRCm39) missense probably damaging 1.00
R8405:Vmn2r97 UTSW 17 19,134,802 (GRCm39) critical splice donor site probably null
R8755:Vmn2r97 UTSW 17 19,168,104 (GRCm39) missense probably damaging 1.00
R8790:Vmn2r97 UTSW 17 19,160,472 (GRCm39) missense probably damaging 1.00
R8850:Vmn2r97 UTSW 17 19,149,607 (GRCm39) missense probably benign 0.00
R9060:Vmn2r97 UTSW 17 19,134,585 (GRCm39) start codon destroyed probably null 0.94
R9079:Vmn2r97 UTSW 17 19,149,640 (GRCm39) missense probably benign
R9252:Vmn2r97 UTSW 17 19,167,849 (GRCm39) missense probably benign 0.00
R9278:Vmn2r97 UTSW 17 19,134,762 (GRCm39) missense probably benign 0.00
R9342:Vmn2r97 UTSW 17 19,149,368 (GRCm39) missense probably benign
R9422:Vmn2r97 UTSW 17 19,149,333 (GRCm39) missense probably benign 0.03
R9496:Vmn2r97 UTSW 17 19,149,227 (GRCm39) missense probably damaging 1.00
R9571:Vmn2r97 UTSW 17 19,149,919 (GRCm39) missense probably benign
R9601:Vmn2r97 UTSW 17 19,134,770 (GRCm39) missense probably benign
R9672:Vmn2r97 UTSW 17 19,149,442 (GRCm39) missense probably benign 0.00
R9773:Vmn2r97 UTSW 17 19,168,221 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- ACCTTCAGAGACTAAACTCCTGATC -3'
(R):5'- CACAGTAGCAAGAGCCATAGTG -3'

Sequencing Primer
(F):5'- TCAGAGACTAAACTCCTGATCTCAAG -3'
(R):5'- GCCATAGTGAAAGCAACTGC -3'
Posted On 2022-11-14