Incidental Mutation 'R4634:Vmn1r231'
ID 349421
Institutional Source Beutler Lab
Gene Symbol Vmn1r231
Ensembl Gene ENSMUSG00000050933
Gene Name vomeronasal 1 receptor 231
Synonyms V1re7
MMRRC Submission 042009-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R4634 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 21109978-21110913 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 21110660 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 85 (V85A)
Ref Sequence ENSEMBL: ENSMUSP00000056228 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061278]
AlphaFold Q8R2A3
Predicted Effect possibly damaging
Transcript: ENSMUST00000061278
AA Change: V85A

PolyPhen 2 Score 0.461 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000056228
Gene: ENSMUSG00000050933
AA Change: V85A

DomainStartEndE-ValueType
Pfam:TAS2R 6 294 1.6e-13 PFAM
Pfam:V1R 36 297 1.6e-27 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000232004
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency 98% (40/41)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb1 A G 15: 74,456,278 (GRCm39) probably benign Het
Atm T C 9: 53,443,033 (GRCm39) T77A probably benign Het
Brd8 T C 18: 34,741,537 (GRCm39) M311V possibly damaging Het
Cand2 T A 6: 115,774,948 (GRCm39) I1052N probably damaging Het
Ccdc121 G A 5: 31,645,435 (GRCm39) R396Q probably benign Het
Ceacam16 T A 7: 19,592,531 (GRCm39) M126L probably benign Het
Chd3 TGCTGCCGCTGCCGC TGCTGCCGCTGCCGCTGCCGC 11: 69,253,013 (GRCm39) probably benign Het
Cln8 C T 8: 14,944,842 (GRCm39) T52I probably damaging Het
Cops2 C A 2: 125,682,400 (GRCm39) D194Y probably damaging Het
Csf1 C T 3: 107,656,483 (GRCm39) V71M probably damaging Het
Dip2b T C 15: 100,058,372 (GRCm39) F183S probably damaging Het
Ears2 T A 7: 121,643,832 (GRCm39) K375N probably benign Het
Fbn1 C A 2: 125,185,981 (GRCm39) G1596C probably damaging Het
Fscn2 A T 11: 120,258,546 (GRCm39) D390V possibly damaging Het
Gm42669 A T 5: 107,656,079 (GRCm39) I781F possibly damaging Het
Gprin1 G T 13: 54,885,871 (GRCm39) P801Q probably damaging Het
Hira C A 16: 18,765,150 (GRCm39) S609R probably damaging Het
Htt G T 5: 35,033,292 (GRCm39) K1853N probably benign Het
Kif2c T C 4: 117,035,437 (GRCm39) I4V probably benign Het
Marveld2 A G 13: 100,748,447 (GRCm39) Y211H probably damaging Het
Myd88 G A 9: 119,167,175 (GRCm39) probably null Het
Nup153 A T 13: 46,840,706 (GRCm39) N967K possibly damaging Het
Or4a76 A C 2: 89,460,516 (GRCm39) I242S possibly damaging Het
Peg10 GC GCTCC 6: 4,756,452 (GRCm39) probably benign Het
Rabepk A G 2: 34,670,752 (GRCm39) M228T probably damaging Het
Rcn3 T A 7: 44,738,092 (GRCm39) D92V probably damaging Het
Sec1 T A 7: 45,328,297 (GRCm39) Y250F probably damaging Het
Slc39a4 T C 15: 76,498,693 (GRCm39) T334A probably benign Het
Trip11 G T 12: 101,803,875 (GRCm39) T1669K probably damaging Het
Ttbk2 A G 2: 120,570,673 (GRCm39) L1091P probably damaging Het
Zfp280b T C 10: 75,874,663 (GRCm39) C181R probably benign Het
Other mutations in Vmn1r231
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00233:Vmn1r231 APN 17 21,110,828 (GRCm39) missense possibly damaging 0.68
IGL02124:Vmn1r231 APN 17 21,110,568 (GRCm39) missense probably damaging 1.00
IGL02151:Vmn1r231 APN 17 21,109,997 (GRCm39) missense probably benign 0.06
R0066:Vmn1r231 UTSW 17 21,109,998 (GRCm39) missense probably benign 0.27
R0066:Vmn1r231 UTSW 17 21,109,998 (GRCm39) missense probably benign 0.27
R0396:Vmn1r231 UTSW 17 21,110,661 (GRCm39) missense probably damaging 0.98
R0427:Vmn1r231 UTSW 17 21,110,490 (GRCm39) missense probably benign 0.05
R0470:Vmn1r231 UTSW 17 21,110,265 (GRCm39) nonsense probably null
R0848:Vmn1r231 UTSW 17 21,110,433 (GRCm39) missense probably damaging 1.00
R1692:Vmn1r231 UTSW 17 21,110,871 (GRCm39) missense probably benign 0.02
R1987:Vmn1r231 UTSW 17 21,110,212 (GRCm39) missense probably damaging 1.00
R1988:Vmn1r231 UTSW 17 21,110,212 (GRCm39) missense probably damaging 1.00
R2105:Vmn1r231 UTSW 17 21,110,380 (GRCm39) missense possibly damaging 0.66
R4440:Vmn1r231 UTSW 17 21,110,718 (GRCm39) missense possibly damaging 0.48
R4646:Vmn1r231 UTSW 17 21,110,571 (GRCm39) missense probably damaging 1.00
R4678:Vmn1r231 UTSW 17 21,110,489 (GRCm39) missense possibly damaging 0.94
R4696:Vmn1r231 UTSW 17 21,110,901 (GRCm39) missense possibly damaging 0.63
R4938:Vmn1r231 UTSW 17 21,110,613 (GRCm39) missense possibly damaging 0.76
R5544:Vmn1r231 UTSW 17 21,110,840 (GRCm39) missense probably damaging 1.00
R5942:Vmn1r231 UTSW 17 21,110,417 (GRCm39) missense possibly damaging 0.83
R6053:Vmn1r231 UTSW 17 21,110,081 (GRCm39) missense probably damaging 1.00
R6692:Vmn1r231 UTSW 17 21,110,745 (GRCm39) missense possibly damaging 0.46
R6712:Vmn1r231 UTSW 17 21,109,992 (GRCm39) missense possibly damaging 0.54
R7131:Vmn1r231 UTSW 17 21,110,140 (GRCm39) missense possibly damaging 0.87
R7854:Vmn1r231 UTSW 17 21,110,894 (GRCm39) missense probably damaging 0.98
R7918:Vmn1r231 UTSW 17 21,110,236 (GRCm39) nonsense probably null
R8187:Vmn1r231 UTSW 17 21,110,893 (GRCm39) missense probably benign 0.10
R8238:Vmn1r231 UTSW 17 21,110,640 (GRCm39) missense probably benign 0.08
R8313:Vmn1r231 UTSW 17 21,110,289 (GRCm39) missense probably benign 0.02
R8525:Vmn1r231 UTSW 17 21,110,001 (GRCm39) missense probably benign 0.06
R9276:Vmn1r231 UTSW 17 21,110,560 (GRCm39) missense probably benign 0.00
RF010:Vmn1r231 UTSW 17 21,110,255 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GGGCCTGTAAATTCATCATGACC -3'
(R):5'- TCATCCTTCAATGTTCAGTGGG -3'

Sequencing Primer
(F):5'- GCCTGTAAATTCATCATGACCTAAAC -3'
(R):5'- CCTTCAATGTTCAGTGGGAATTC -3'
Posted On 2015-10-08