Incidental Mutation 'R4807:Vmn1r213'
ID 370787
Institutional Source Beutler Lab
Gene Symbol Vmn1r213
Ensembl Gene ENSMUSG00000060024
Gene Name vomeronasal 1 receptor 213
Synonyms V1rh6
MMRRC Submission 042426-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R4807 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 23195419-23196573 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 23195775 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Stop codon at position 119 (W119*)
Ref Sequence ENSEMBL: ENSMUSP00000153766 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076897] [ENSMUST00000227573] [ENSMUST00000228031] [ENSMUST00000228758]
AlphaFold Q8R278
Predicted Effect probably null
Transcript: ENSMUST00000076897
AA Change: W119*
SMART Domains Protein: ENSMUSP00000076163
Gene: ENSMUSG00000060024
AA Change: W119*

DomainStartEndE-ValueType
transmembrane domain 95 117 N/A INTRINSIC
Pfam:V1R 118 382 4.3e-31 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000227573
AA Change: W33*
Predicted Effect probably null
Transcript: ENSMUST00000228031
AA Change: W33*
Predicted Effect probably null
Transcript: ENSMUST00000228758
AA Change: W119*
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.2%
Validation Efficiency 98% (86/88)
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 C T 7: 120,139,832 (GRCm39) A1499V probably damaging Het
Agap3 T A 5: 24,682,114 (GRCm39) D386E probably damaging Het
Ahdc1 C A 4: 132,791,624 (GRCm39) T955K possibly damaging Het
Ankrd9 A G 12: 110,943,669 (GRCm39) Y122H probably benign Het
Apc2 G T 10: 80,150,196 (GRCm39) R1721L probably benign Het
Arfgef3 A G 10: 18,522,385 (GRCm39) V547A probably benign Het
Arhgap42 T C 9: 9,046,629 (GRCm39) N203D possibly damaging Het
Arl6ip1 AAAATAAATAAATAAATAAATAAATA AAAATAAATAAATAAATAAATAAATAAATA 7: 117,721,122 (GRCm39) probably benign Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Aspm T A 1: 139,405,657 (GRCm39) F1515I probably damaging Het
Baz1a T C 12: 54,945,267 (GRCm39) T1363A probably benign Het
Cacng3 C T 7: 122,353,732 (GRCm39) A72V probably benign Het
Casp8ap2 T C 4: 32,644,505 (GRCm39) C1193R possibly damaging Het
Ccr3 A G 9: 123,829,334 (GRCm39) Y223C probably damaging Het
Clcn3 C A 8: 61,387,564 (GRCm39) L201F probably damaging Het
Cltc A C 11: 86,591,902 (GRCm39) probably benign Het
Cyp19a1 G T 9: 54,083,930 (GRCm39) T86K possibly damaging Het
Ddx24 A T 12: 103,385,720 (GRCm39) F248L probably damaging Het
Ddx60 G A 8: 62,432,372 (GRCm39) V885I probably damaging Het
Dync2h1 T C 9: 7,139,422 (GRCm39) I1404M probably benign Het
Emilin2 A T 17: 71,580,443 (GRCm39) V761E probably damaging Het
Endou C T 15: 97,629,113 (GRCm39) C13Y probably benign Het
Ep400 C A 5: 110,843,444 (GRCm39) probably null Het
Fbxo33 C A 12: 59,265,998 (GRCm39) D90Y probably damaging Het
Fryl A G 5: 73,198,705 (GRCm39) F2641L probably benign Het
Gbp2b A G 3: 142,304,006 (GRCm39) I34V probably benign Het
Ghdc T C 11: 100,661,051 (GRCm39) H38R probably damaging Het
Gm10722 T C 9: 3,000,937 (GRCm39) C6R probably benign Het
Gpr63 A C 4: 25,007,446 (GRCm39) M57L probably benign Het
Gprc5c A G 11: 114,755,324 (GRCm39) S3G probably damaging Het
Grk4 A T 5: 34,909,552 (GRCm39) M539L probably benign Het
Gulo C T 14: 66,227,833 (GRCm39) M366I probably benign Het
Heatr5a T C 12: 51,924,303 (GRCm39) H1970R probably damaging Het
Hmbox1 T C 14: 65,062,998 (GRCm39) probably benign Het
Ighg2b T C 12: 113,267,965 (GRCm39) probably benign Het
Il1b A T 2: 129,212,226 (GRCm39) C9S probably benign Het
Itpkb A T 1: 180,162,440 (GRCm39) probably benign Het
Kcnn1 T A 8: 71,300,822 (GRCm39) H473L probably damaging Het
Kidins220 C T 12: 25,107,284 (GRCm39) S1579L probably damaging Het
Kif1b A T 4: 149,332,378 (GRCm39) probably benign Het
Lyg2 A T 1: 37,950,148 (GRCm39) M60K possibly damaging Het
Mak16 G T 8: 31,656,161 (GRCm39) H107Q probably benign Het
Mapkap1 G A 2: 34,487,434 (GRCm39) probably null Het
Mastl A G 2: 23,022,855 (GRCm39) S623P probably benign Het
Mccc1 T C 3: 36,039,195 (GRCm39) Y46C probably damaging Het
Mdn1 T G 4: 32,685,651 (GRCm39) probably null Het
Med25 T A 7: 44,534,043 (GRCm39) T31S probably benign Het
Mprip G A 11: 59,648,846 (GRCm39) G850D probably benign Het
Mrpl10 T C 11: 96,932,449 (GRCm39) I8T probably benign Het
Msr1 T C 8: 40,095,668 (GRCm39) probably benign Het
Myo3b T A 2: 69,936,056 (GRCm39) I99N probably damaging Het
Neurod6 A T 6: 55,655,640 (GRCm39) N332K probably damaging Het
Npc1l1 T C 11: 6,168,723 (GRCm39) Y886C probably damaging Het
Nsmaf T C 4: 6,398,542 (GRCm39) probably null Het
Ntn4 C T 10: 93,480,362 (GRCm39) R29C probably damaging Het
Or5d47 T A 2: 87,804,095 (GRCm39) I305L probably benign Het
Plppr2 A G 9: 21,855,810 (GRCm39) N261S probably damaging Het
Prkar2a T A 9: 108,617,584 (GRCm39) probably benign Het
Pxk G A 14: 8,144,133 (GRCm38) V294M probably damaging Het
Rars1 A G 11: 35,699,973 (GRCm39) F608L possibly damaging Het
Rasa3 A G 8: 13,664,633 (GRCm39) F60L probably damaging Het
Rbm47 C T 5: 66,176,647 (GRCm39) A490T possibly damaging Het
Sardh T C 2: 27,079,539 (GRCm39) I918V probably benign Het
Saxo5 A G 8: 3,529,004 (GRCm39) K193R possibly damaging Het
Sdhc T C 1: 170,963,626 (GRCm39) Y80C probably damaging Het
Selp T A 1: 163,971,505 (GRCm39) M653K probably damaging Het
Slc6a17 T C 3: 107,407,803 (GRCm39) D56G possibly damaging Het
Slco1b2 T C 6: 141,615,195 (GRCm39) S367P probably damaging Het
Spry4 TTGAGGTCC T 18: 38,723,328 (GRCm39) probably null Het
Strip2 T A 6: 29,925,092 (GRCm39) Y143* probably null Het
Sycp2 T C 2: 178,035,754 (GRCm39) probably benign Het
Tex30 C A 1: 44,126,118 (GRCm39) V204L possibly damaging Het
Tln2 G T 9: 67,239,015 (GRCm39) T1087K probably benign Het
Tmeff2 A C 1: 51,018,546 (GRCm39) N176T probably benign Het
Togaram2 C G 17: 72,004,918 (GRCm39) T324R probably damaging Het
Trpc3 C T 3: 36,688,531 (GRCm39) R836Q probably benign Het
Trpm7 A C 2: 126,673,149 (GRCm39) L535V probably benign Het
Vps29 T G 5: 122,500,951 (GRCm39) V176G probably damaging Het
Vsig10l A G 7: 43,113,173 (GRCm39) T144A possibly damaging Het
Wdr11 T C 7: 129,229,746 (GRCm39) Y844H probably benign Het
Zbp1 A T 2: 173,053,999 (GRCm39) M174K probably damaging Het
Zfp341 G A 2: 154,487,786 (GRCm39) probably benign Het
Zfp638 G A 6: 83,920,040 (GRCm39) R546H probably damaging Het
Zfp820 A T 17: 22,042,853 (GRCm39) M1K probably null Het
Other mutations in Vmn1r213
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0018:Vmn1r213 UTSW 13 23,196,311 (GRCm39) missense probably damaging 1.00
R0094:Vmn1r213 UTSW 13 23,195,819 (GRCm39) missense probably damaging 1.00
R0324:Vmn1r213 UTSW 13 23,195,588 (GRCm39) intron probably benign
R0389:Vmn1r213 UTSW 13 23,195,932 (GRCm39) missense probably benign 0.00
R0650:Vmn1r213 UTSW 13 23,195,564 (GRCm39) intron probably benign
R0652:Vmn1r213 UTSW 13 23,195,564 (GRCm39) intron probably benign
R1902:Vmn1r213 UTSW 13 23,196,476 (GRCm39) missense possibly damaging 0.87
R1996:Vmn1r213 UTSW 13 23,196,473 (GRCm39) missense probably benign 0.02
R1997:Vmn1r213 UTSW 13 23,196,473 (GRCm39) missense probably benign 0.02
R4214:Vmn1r213 UTSW 13 23,196,173 (GRCm39) missense possibly damaging 0.95
R4409:Vmn1r213 UTSW 13 23,195,593 (GRCm39) intron probably benign
R4650:Vmn1r213 UTSW 13 23,196,422 (GRCm39) missense possibly damaging 0.80
R4685:Vmn1r213 UTSW 13 23,195,800 (GRCm39) missense probably benign 0.05
R4698:Vmn1r213 UTSW 13 23,195,507 (GRCm39) intron probably benign
R4799:Vmn1r213 UTSW 13 23,196,016 (GRCm39) missense probably damaging 1.00
R5853:Vmn1r213 UTSW 13 23,195,684 (GRCm39) missense probably benign 0.32
R7389:Vmn1r213 UTSW 13 23,196,556 (GRCm39) missense probably benign 0.18
R7414:Vmn1r213 UTSW 13 23,195,446 (GRCm39) missense unknown
R8054:Vmn1r213 UTSW 13 23,195,910 (GRCm39) missense possibly damaging 0.93
R9069:Vmn1r213 UTSW 13 23,196,043 (GRCm39) missense probably damaging 1.00
R9155:Vmn1r213 UTSW 13 23,196,343 (GRCm39) nonsense probably null
R9428:Vmn1r213 UTSW 13 23,195,944 (GRCm39) missense
R9469:Vmn1r213 UTSW 13 23,196,101 (GRCm39) missense probably benign 0.22
R9633:Vmn1r213 UTSW 13 23,195,519 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCAGTTCAGATCCATGTCTAGC -3'
(R):5'- ACTGATGATGATGGCCTGGAC -3'

Sequencing Primer
(F):5'- GTTCAGATCCATGTCTAGCATTACTG -3'
(R):5'- ATGATGGCCTGGACCACAGTG -3'
Posted On 2016-02-04