Incidental Mutation 'R9439:Vmn1r210'
ID 713456
Institutional Source Beutler Lab
Gene Symbol Vmn1r210
Ensembl Gene ENSMUSG00000061296
Gene Name vomeronasal 1 receptor 210
Synonyms V1rh10
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R9439 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 23011364-23012284 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 23011397 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 296 (H296Q)
Ref Sequence ENSEMBL: ENSMUSP00000071925 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072044] [ENSMUST00000226180] [ENSMUST00000226294]
AlphaFold Q8R274
Predicted Effect possibly damaging
Transcript: ENSMUST00000072044
AA Change: H296Q

PolyPhen 2 Score 0.663 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000071925
Gene: ENSMUSG00000061296
AA Change: H296Q

DomainStartEndE-ValueType
Pfam:V1R 34 297 8.6e-38 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000226180
AA Change: H296Q

PolyPhen 2 Score 0.663 (Sensitivity: 0.86; Specificity: 0.91)
Predicted Effect possibly damaging
Transcript: ENSMUST00000226294
AA Change: H296Q

PolyPhen 2 Score 0.663 (Sensitivity: 0.86; Specificity: 0.91)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A T 3: 137,772,048 (GRCm39) E412D probably benign Het
Aak1 T A 6: 86,933,274 (GRCm39) V415D probably damaging Het
Ache A C 5: 137,289,185 (GRCm39) D297A probably damaging Het
Armc9 T C 1: 86,084,687 (GRCm39) I4T possibly damaging Het
Atp8b2 T A 3: 89,851,492 (GRCm39) Y925F Het
Avpr1b T C 1: 131,528,029 (GRCm39) L184P probably damaging Het
Cabin1 G A 10: 75,581,069 (GRCm39) P419L probably damaging Het
Ccdc88c T C 12: 100,884,597 (GRCm39) S1578G probably benign Het
Ccnd2 A T 6: 127,127,617 (GRCm39) C40* probably null Het
Col6a3 A T 1: 90,744,155 (GRCm39) I471N probably damaging Het
Cp A G 3: 20,046,671 (GRCm39) probably null Het
Cyfip2 C T 11: 46,091,668 (GRCm39) R1084Q probably damaging Het
Diaph1 A G 18: 38,029,412 (GRCm39) probably null Het
Dnah6 T C 6: 73,012,330 (GRCm39) N3713S possibly damaging Het
Dot1l G T 10: 80,621,438 (GRCm39) R633L possibly damaging Het
Ehmt1 A T 2: 24,715,030 (GRCm39) M809K probably damaging Het
Fcgbp C A 7: 27,803,436 (GRCm39) A1680E possibly damaging Het
Flt1 A G 5: 147,515,207 (GRCm39) F1072L probably damaging Het
Gm19410 G T 8: 36,248,810 (GRCm39) A549S probably damaging Het
Gm57859 C T 11: 113,583,229 (GRCm39) Q519* probably null Het
Gnat1 A T 9: 107,553,511 (GRCm39) I249N Het
Gp2 T C 7: 119,053,433 (GRCm39) Y176C probably damaging Het
Gpc2 G T 5: 138,277,248 (GRCm39) Q60K probably benign Het
Gpsm2 T A 3: 108,610,397 (GRCm39) E21V probably damaging Het
Igkv4-80 T A 6: 68,993,793 (GRCm39) M33L probably benign Het
Il20ra C A 10: 19,618,751 (GRCm39) H66Q probably benign Het
Kap C T 6: 133,828,950 (GRCm39) D61N probably benign Het
Magi3 C T 3: 103,922,473 (GRCm39) A1415T probably benign Het
Mpp7 A T 18: 7,461,692 (GRCm39) Y60* probably null Het
Neil1 T A 9: 57,051,098 (GRCm39) R294* probably null Het
Nkx6-3 A G 8: 23,643,778 (GRCm39) S60G probably benign Het
Noc2l T A 4: 156,326,130 (GRCm39) S406T possibly damaging Het
Or11m3 T C 15: 98,396,247 (GRCm39) V298A possibly damaging Het
Or14j2 A G 17: 37,885,825 (GRCm39) I163T probably benign Het
Or2h2c A G 17: 37,422,205 (GRCm39) V223A probably damaging Het
Or2t46 T C 11: 58,472,104 (GRCm39) C145R probably benign Het
Or51ac3 T G 7: 103,214,049 (GRCm39) I146L probably benign Het
Or5p81 T C 7: 108,266,626 (GRCm39) M1T probably null Het
Paqr4 A G 17: 23,958,939 (GRCm39) F21L probably damaging Het
Pcdha9 A G 18: 37,131,527 (GRCm39) T199A probably benign Het
Pcdhgb7 T C 18: 37,884,917 (GRCm39) L29P probably benign Het
Pfkl G A 10: 77,831,172 (GRCm39) A323V probably damaging Het
Pik3r4 C A 9: 105,528,041 (GRCm39) P465T probably damaging Het
Pitpnm2 A G 5: 124,274,189 (GRCm39) S307P probably damaging Het
Pitpnm2 A G 5: 124,278,659 (GRCm39) Y191H probably damaging Het
Plod3 G A 5: 137,023,036 (GRCm39) V613I probably benign Het
Prr23a2 C T 9: 98,738,921 (GRCm39) T93I probably damaging Het
Ptk6 T A 2: 180,840,206 (GRCm39) M267L possibly damaging Het
Rabl6 C T 2: 25,492,432 (GRCm39) probably null Het
Ralgapa2 T C 2: 146,254,058 (GRCm39) H787R probably benign Het
Rfx8 T G 1: 39,724,669 (GRCm39) M231L probably benign Het
Rnf126 A T 10: 79,597,465 (GRCm39) I149N probably damaging Het
Smpd4 A G 16: 17,459,451 (GRCm39) I625V probably benign Het
Tcf7l1 A G 6: 72,765,740 (GRCm39) S66P probably damaging Het
Tsc22d1 G A 14: 76,743,899 (GRCm39) V1007M probably damaging Het
Tspoap1 C T 11: 87,665,535 (GRCm39) R758C probably damaging Het
Zfp532 G A 18: 65,818,714 (GRCm39) V857I probably benign Het
Zfyve9 T C 4: 108,501,538 (GRCm39) T593A probably benign 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
R0629:Vmn1r210 UTSW 13 23,012,044 (GRCm39) missense probably damaging 1.00
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
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'- TCTATATCACTGTAATTTGCCAAGGTC -3'
(R):5'- AGAGCTGCTCAAAGTGTCCTC -3'

Sequencing Primer
(F):5'- ACTGTAATTTGCCAAGGTCATTCTC -3'
(R):5'- AAAGTGTCCTCCTTCTGATGC -3'
Posted On 2022-05-16