Incidental Mutation 'R0655:Vmn1r85'
ID 62479
Institutional Source Beutler Lab
Gene Symbol Vmn1r85
Ensembl Gene ENSMUSG00000070817
Gene Name vomeronasal 1 receptor 85
Synonyms V1rj3
MMRRC Submission 038840-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R0655 (G1)
Quality Score 113
Status Not validated
Chromosome 7
Chromosomal Location 12818216-12819142 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 12818650 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 165 (Y165H)
Ref Sequence ENSEMBL: ENSMUSP00000148178 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094829] [ENSMUST00000209822]
AlphaFold Q8VIB8
Predicted Effect probably damaging
Transcript: ENSMUST00000094829
AA Change: Y165H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000092424
Gene: ENSMUSG00000070817
AA Change: Y165H

DomainStartEndE-ValueType
Pfam:TAS2R 1 296 8.4e-18 PFAM
Pfam:V1R 24 298 2.5e-36 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000209822
AA Change: Y165H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 99.0%
  • 10x: 97.7%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 G C 17: 36,268,737 (GRCm39) I757M probably benign Het
Abtb3 A G 10: 85,481,390 (GRCm39) T931A probably damaging Het
Atg16l1 T A 1: 87,694,551 (GRCm39) I76N probably damaging Het
Baz1b T A 5: 135,271,284 (GRCm39) I1289N probably benign Het
Bcl2l15 T A 3: 103,740,285 (GRCm39) probably null Het
Cbl G T 9: 44,070,049 (GRCm39) T566K probably damaging Het
Cd96 T C 16: 45,919,482 (GRCm39) K180E probably benign Het
Cpxm2 G A 7: 131,656,549 (GRCm39) T571I possibly damaging Het
Cyp2a12 A T 7: 26,736,046 (GRCm39) Y485F probably benign Het
Cyp4f17 T A 17: 32,743,871 (GRCm39) Y350N possibly damaging Het
Dstn T A 2: 143,780,342 (GRCm39) I14N probably damaging Het
Eea1 A G 10: 95,831,460 (GRCm39) S184G probably benign Het
Eif1a G T 18: 46,741,130 (GRCm39) G122C probably damaging Het
Esf1 T A 2: 139,990,799 (GRCm39) T562S probably benign Het
Fem1c G A 18: 46,638,227 (GRCm39) R592C probably benign Het
Fig4 T C 10: 41,161,673 (GRCm39) N30S probably damaging Het
Gria2 C A 3: 80,639,377 (GRCm39) E212* probably null Het
Gsdmc2 C T 15: 63,699,622 (GRCm39) A269T probably benign Het
Herc4 T C 10: 63,109,350 (GRCm39) V195A probably benign Het
Hivep1 T C 13: 42,321,061 (GRCm39) S2123P probably damaging Het
Hspa4 T C 11: 53,160,519 (GRCm39) E519G probably benign Het
Htr2b A G 1: 86,038,565 (GRCm39) S14P probably benign Het
Ifit1 T C 19: 34,625,047 (GRCm39) V61A probably damaging Het
Ifitm1 C A 7: 140,549,449 (GRCm39) F77L probably benign Het
Matn2 T C 15: 34,345,346 (GRCm39) S118P probably benign Het
Mtmr3 C A 11: 4,438,610 (GRCm39) D615Y probably damaging Het
Mtss1 C A 15: 58,953,351 (GRCm39) C9F probably damaging Het
Muc5b A T 7: 141,417,679 (GRCm39) I3542F probably benign Het
Nwd2 T C 5: 63,948,928 (GRCm39) S167P possibly damaging Het
Or1e34 T C 11: 73,778,631 (GRCm39) D189G possibly damaging Het
Or2ag1b A T 7: 106,288,632 (GRCm39) F102Y probably damaging Het
Or8b54 C T 9: 38,686,850 (GRCm39) Q100* probably null Het
Oscp1 T C 4: 125,952,526 (GRCm39) L18P probably damaging Het
Pax5 A G 4: 44,537,462 (GRCm39) S297P probably damaging Het
Phldb3 A T 7: 24,323,797 (GRCm39) D476V probably benign Het
Phlpp2 A T 8: 110,622,219 (GRCm39) I154L probably benign Het
Prx T A 7: 27,216,846 (GRCm39) V449E probably damaging Het
Psd3 A G 8: 68,416,341 (GRCm39) S519P probably benign Het
Rnf138 T G 18: 21,143,840 (GRCm39) V128G probably benign Het
Safb T A 17: 56,904,803 (GRCm39) S209T probably benign Het
Sbno1 C A 5: 124,514,212 (GRCm39) V1327L possibly damaging Het
Scarb1 A G 5: 125,377,504 (GRCm39) V176A probably damaging Het
Scd4 A G 19: 44,327,407 (GRCm39) H161R possibly damaging Het
Selenoo T A 15: 88,979,858 (GRCm39) H335Q probably damaging Het
Slfn8 A G 11: 82,894,647 (GRCm39) F664S probably benign Het
Spef2 T C 15: 9,626,217 (GRCm39) I1116M possibly damaging Het
Taf2 G A 15: 54,901,690 (GRCm39) R835W probably damaging Het
Tdrd9 A G 12: 112,006,899 (GRCm39) E921G probably damaging Het
Tectb G A 19: 55,178,302 (GRCm39) G234S possibly damaging Het
Tmc1 C T 19: 20,776,540 (GRCm39) M606I probably damaging Het
Tmed10 T A 12: 85,390,291 (GRCm39) I88F probably damaging Het
Tnfrsf11a G A 1: 105,735,880 (GRCm39) V31I unknown Het
Trp53inp2 G T 2: 155,228,088 (GRCm39) G98* probably null Het
Tssc4 A G 7: 142,623,782 (GRCm39) D30G probably damaging Het
Uaca T C 9: 60,779,311 (GRCm39) Y1233H probably benign Het
Unc13c G A 9: 73,838,235 (GRCm39) T872I probably damaging Het
Unc80 A G 1: 66,542,940 (GRCm39) H398R probably damaging Het
Vmn1r64 G A 7: 5,887,207 (GRCm39) T112I probably benign Het
Vmn2r72 A T 7: 85,387,319 (GRCm39) C748* probably null Het
Wdr17 A G 8: 55,102,233 (GRCm39) W929R probably damaging Het
Yeats2 A T 16: 20,012,574 (GRCm39) K591* probably null Het
Zbtb9 T A 17: 27,193,074 (GRCm39) S160T probably damaging Het
Znfx1 T A 2: 166,898,827 (GRCm39) R32S probably damaging Het
Zng1 T C 19: 24,930,684 (GRCm39) M122V possibly damaging Het
Other mutations in Vmn1r85
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01099:Vmn1r85 APN 7 12,818,461 (GRCm39) nonsense probably null
IGL01520:Vmn1r85 APN 7 12,819,081 (GRCm39) missense probably damaging 1.00
IGL01803:Vmn1r85 APN 7 12,818,496 (GRCm39) missense probably damaging 0.98
IGL02285:Vmn1r85 APN 7 12,818,711 (GRCm39) missense probably damaging 1.00
IGL02852:Vmn1r85 APN 7 12,819,010 (GRCm39) missense possibly damaging 0.70
IGL03012:Vmn1r85 APN 7 12,818,692 (GRCm39) missense probably benign 0.01
R0391:Vmn1r85 UTSW 7 12,818,515 (GRCm39) missense probably benign 0.01
R1142:Vmn1r85 UTSW 7 12,818,481 (GRCm39) missense probably benign 0.01
R1452:Vmn1r85 UTSW 7 12,818,808 (GRCm39) missense probably damaging 1.00
R1942:Vmn1r85 UTSW 7 12,818,668 (GRCm39) missense possibly damaging 0.83
R3760:Vmn1r85 UTSW 7 12,818,932 (GRCm39) missense probably damaging 0.96
R4783:Vmn1r85 UTSW 7 12,818,788 (GRCm39) missense probably damaging 1.00
R4785:Vmn1r85 UTSW 7 12,818,788 (GRCm39) missense probably damaging 1.00
R5373:Vmn1r85 UTSW 7 12,818,255 (GRCm39) nonsense probably null
R6021:Vmn1r85 UTSW 7 12,818,616 (GRCm39) missense probably benign 0.00
R6035:Vmn1r85 UTSW 7 12,818,854 (GRCm39) missense probably damaging 1.00
R6035:Vmn1r85 UTSW 7 12,818,854 (GRCm39) missense probably damaging 1.00
R6834:Vmn1r85 UTSW 7 12,818,571 (GRCm39) missense probably damaging 1.00
R7340:Vmn1r85 UTSW 7 12,819,073 (GRCm39) missense probably damaging 1.00
R7346:Vmn1r85 UTSW 7 12,818,964 (GRCm39) missense probably damaging 0.99
R7836:Vmn1r85 UTSW 7 12,818,698 (GRCm39) missense probably benign 0.06
R7896:Vmn1r85 UTSW 7 12,818,448 (GRCm39) missense probably benign 0.22
R9090:Vmn1r85 UTSW 7 12,818,942 (GRCm39) nonsense probably null
R9271:Vmn1r85 UTSW 7 12,818,942 (GRCm39) nonsense probably null
R9354:Vmn1r85 UTSW 7 12,818,725 (GRCm39) missense probably damaging 1.00
R9713:Vmn1r85 UTSW 7 12,818,458 (GRCm39) missense probably damaging 1.00
R9779:Vmn1r85 UTSW 7 12,818,308 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- GCAGTTTACAAGCAACAGGATTGTGTG -3'
(R):5'- TCAAAGCTCGCTTTAACAGACAGATCG -3'

Sequencing Primer
(F):5'- CAACAGGATTGTGTGAGTGGC -3'
(R):5'- CCATTTTCATGCACCTGATGATAG -3'
Posted On 2013-07-30