Incidental Mutation 'R0629:Vmn1r210'
ID 57778
Institutional Source Beutler Lab
Gene Symbol Vmn1r210
Ensembl Gene ENSMUSG00000061296
Gene Name vomeronasal 1 receptor 210
Synonyms V1rh10
MMRRC Submission 038818-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R0629 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 23011364-23012284 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 23012044 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 81 (K81E)
Ref Sequence ENSEMBL: ENSMUSP00000153776 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072044] [ENSMUST00000226180] [ENSMUST00000226294]
AlphaFold Q8R274
Predicted Effect probably damaging
Transcript: ENSMUST00000072044
AA Change: K81E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000071925
Gene: ENSMUSG00000061296
AA Change: K81E

DomainStartEndE-ValueType
Pfam:V1R 34 297 8.6e-38 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000226180
AA Change: K81E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000226294
AA Change: K81E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.6%
  • 20x: 95.6%
Validation Efficiency 100% (66/66)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars2 A T 17: 45,818,473 (GRCm39) D86V probably damaging Het
Adamts14 G A 10: 61,047,403 (GRCm39) Q733* probably null Het
Adcy10 A G 1: 165,370,674 (GRCm39) D651G probably damaging Het
Apcdd1 T A 18: 63,067,041 (GRCm39) C52S probably damaging Het
Bclaf1 T C 10: 20,209,172 (GRCm39) S463P probably damaging Het
Cabcoco1 T C 10: 68,352,108 (GRCm39) Y68C probably damaging Het
Cacna1f G A X: 7,486,673 (GRCm39) S888N probably damaging Het
Cacna1g A G 11: 94,300,369 (GRCm39) C2134R possibly damaging Het
Cdc37 A C 9: 21,052,064 (GRCm39) M325R possibly damaging Het
Clca3a2 T A 3: 144,778,000 (GRCm39) M762L probably benign Het
Cntn3 C T 6: 102,180,937 (GRCm39) V753M probably damaging Het
Col6a6 A T 9: 105,604,364 (GRCm39) probably benign Het
Dscaml1 A G 9: 45,632,716 (GRCm39) D1194G probably damaging Het
Egfr G A 11: 16,819,333 (GRCm39) G288S probably damaging Het
Fbxl17 G T 17: 63,778,409 (GRCm39) N19K probably damaging Het
Fmo3 A G 1: 162,785,796 (GRCm39) probably benign Het
Frmd6 T C 12: 70,930,536 (GRCm39) Y219H probably damaging Het
Fuca1 T C 4: 135,652,955 (GRCm39) V193A possibly damaging Het
Gm7461 C T 8: 4,727,769 (GRCm39) noncoding transcript Het
Gpc5 T A 14: 115,789,651 (GRCm39) N508K possibly damaging Het
Iqch A T 9: 63,332,664 (GRCm39) D1019E probably benign Het
Isyna1 A G 8: 71,047,358 (GRCm39) Y27C probably damaging Het
Itgb8 T G 12: 119,166,216 (GRCm39) H105P probably benign Het
Kbtbd11 C T 8: 15,077,572 (GRCm39) P57L probably benign Het
Kcns3 A C 12: 11,142,559 (GRCm39) C47G probably damaging Het
Kif21b A T 1: 136,099,895 (GRCm39) probably null Het
Lama3 A T 18: 12,552,302 (GRCm39) H418L possibly damaging Het
Lrit3 A G 3: 129,581,951 (GRCm39) Y679H probably damaging Het
Lrrc19 T A 4: 94,526,489 (GRCm39) D356V probably damaging Het
Morc2b A G 17: 33,354,781 (GRCm39) M997T probably benign Het
Mroh9 T C 1: 162,888,205 (GRCm39) H290R possibly damaging Het
Mtcl1 A T 17: 66,645,137 (GRCm39) S1886T possibly damaging Het
Muc20 T C 16: 32,613,791 (GRCm39) T529A possibly damaging Het
Myo7a A C 7: 97,734,673 (GRCm39) L607R probably damaging Het
Myom2 T A 8: 15,119,783 (GRCm39) F180I probably damaging Het
Myt1l G A 12: 29,861,484 (GRCm39) E89K unknown Het
Nek2 A G 1: 191,563,429 (GRCm39) N431S probably benign Het
Oprm1 A T 10: 6,782,604 (GRCm39) probably null Het
Or2aj4 A T 16: 19,384,730 (GRCm39) V301E possibly damaging Het
Or5t7 T A 2: 86,506,873 (GRCm39) H268L possibly damaging Het
Oxsr1 A G 9: 119,070,850 (GRCm39) probably benign Het
Pasd1 G C X: 70,982,379 (GRCm39) R296P possibly damaging Het
Pdgfrb G A 18: 61,211,720 (GRCm39) probably null Het
Proser1 C A 3: 53,386,485 (GRCm39) P789Q probably benign Het
Ptgs2 A G 1: 149,976,788 (GRCm39) Q7R probably benign Het
Rab3d A G 9: 21,825,982 (GRCm39) V144A probably benign Het
Ralgapb T A 2: 158,281,467 (GRCm39) L167H probably damaging Het
Ranbp3 A G 17: 57,015,200 (GRCm39) T301A possibly damaging Het
Rasgrf1 G A 9: 89,866,322 (GRCm39) V587M probably damaging Het
Sec16b A G 1: 157,392,433 (GRCm39) probably benign Het
Sin3b T C 8: 73,480,164 (GRCm39) probably benign Het
Slc10a2 T C 8: 5,148,562 (GRCm39) S128G probably benign Het
Tbl1xr1 G A 3: 22,264,565 (GRCm39) V507I probably benign Het
Tmem8b T G 4: 43,669,896 (GRCm39) probably null Het
Trak1 A T 9: 121,196,233 (GRCm39) T22S probably benign Het
Trim30d A G 7: 104,136,862 (GRCm39) I114T probably damaging Het
Ttc13 A T 8: 125,401,105 (GRCm39) S624T probably damaging Het
Ttn T C 2: 76,658,474 (GRCm39) probably benign Het
Vipr1 T A 9: 121,489,237 (GRCm39) Y99* probably null Het
Wwc1 T C 11: 35,744,299 (GRCm39) Y841C probably benign Het
Xrcc4 A G 13: 90,149,024 (GRCm39) probably benign Het
Zdhhc22 A T 12: 87,035,071 (GRCm39) I127N probably damaging Het
Zdhhc7 A G 8: 120,814,785 (GRCm39) L8P possibly damaging Het
Zfp664 C A 5: 124,962,659 (GRCm39) L18I probably damaging Het
Other mutations in Vmn1r210
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00938:Vmn1r210 APN 13 23,011,538 (GRCm39) nonsense probably null
IGL01541:Vmn1r210 APN 13 23,011,778 (GRCm39) missense probably benign
IGL01610:Vmn1r210 APN 13 23,011,977 (GRCm39) missense probably damaging 1.00
IGL01632:Vmn1r210 APN 13 23,011,366 (GRCm39) makesense probably null
IGL03268:Vmn1r210 APN 13 23,011,405 (GRCm39) missense probably benign 0.40
IGL03340:Vmn1r210 APN 13 23,011,644 (GRCm39) missense probably benign 0.23
R0227:Vmn1r210 UTSW 13 23,011,561 (GRCm39) missense probably benign 0.02
R3792:Vmn1r210 UTSW 13 23,011,573 (GRCm39) missense probably damaging 1.00
R4125:Vmn1r210 UTSW 13 23,011,779 (GRCm39) missense probably benign 0.00
R4132:Vmn1r210 UTSW 13 23,011,819 (GRCm39) missense probably benign 0.00
R4773:Vmn1r210 UTSW 13 23,011,374 (GRCm39) missense probably benign 0.00
R5653:Vmn1r210 UTSW 13 23,011,378 (GRCm39) nonsense probably null
R6128:Vmn1r210 UTSW 13 23,012,277 (GRCm39) nonsense probably null
R6452:Vmn1r210 UTSW 13 23,011,840 (GRCm39) missense probably damaging 1.00
R6501:Vmn1r210 UTSW 13 23,011,705 (GRCm39) missense possibly damaging 0.90
R6864:Vmn1r210 UTSW 13 23,011,713 (GRCm39) missense probably benign 0.06
R7623:Vmn1r210 UTSW 13 23,011,405 (GRCm39) missense probably benign 0.40
R7991:Vmn1r210 UTSW 13 23,011,684 (GRCm39) missense probably benign 0.01
R9244:Vmn1r210 UTSW 13 23,012,089 (GRCm39) missense probably benign 0.02
R9439:Vmn1r210 UTSW 13 23,011,397 (GRCm39) missense possibly damaging 0.66
R9538:Vmn1r210 UTSW 13 23,011,837 (GRCm39) nonsense probably null
R9732:Vmn1r210 UTSW 13 23,011,379 (GRCm39) missense possibly damaging 0.75
R9794:Vmn1r210 UTSW 13 23,011,432 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- TGGAAGGATGTGCCATGCAGAC -3'
(R):5'- GTGCAAAATGTGCTGTCCAGACC -3'

Sequencing Primer
(F):5'- CCATGCAGACTTTGGCTTG -3'
(R):5'- GATACATCCTGGACACAGGTTTTTC -3'
Posted On 2013-07-11