Incidental Mutation 'R3938:Vmn1r35'
ID 307270
Institutional Source Beutler Lab
Gene Symbol Vmn1r35
Ensembl Gene ENSMUSG00000060699
Gene Name vomeronasal 1 receptor 35
Synonyms V1rc12
MMRRC Submission 040825-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock # R3938 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 66678070-66685906 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 66679073 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Arginine to Serine at position 204 (R204S)
Ref Sequence ENSEMBL: ENSMUSP00000154707 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071414] [ENSMUST00000227346] [ENSMUST00000227354] [ENSMUST00000227749] [ENSMUST00000227961]
AlphaFold Q8R2E2
Predicted Effect probably damaging
Transcript: ENSMUST00000071414
AA Change: R204S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000071362
Gene: ENSMUSG00000060699
AA Change: R204S

DomainStartEndE-ValueType
Pfam:V1R 28 293 1.2e-54 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000227346
AA Change: R37S

PolyPhen 2 Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
Predicted Effect probably damaging
Transcript: ENSMUST00000227354
AA Change: R204S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000227749
AA Change: R204S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227961
AA Change: R37S

PolyPhen 2 Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency 98% (57/58)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik C T 7: 28,154,294 P1561L probably damaging Het
Adamts1 C T 16: 85,795,619 V634M possibly damaging Het
Arid4b A T 13: 14,186,928 N659I probably benign Het
BC049715 T C 6: 136,840,455 I231T possibly damaging Het
Bmp4 T C 14: 46,384,079 Y336C probably damaging Het
Ccdc30 G A 4: 119,352,673 T293I probably benign Het
Chd5 A T 4: 152,377,055 T1275S probably benign Het
Chtf8 A T 8: 106,885,905 M134K probably benign Het
Col11a2 A T 17: 34,039,625 probably benign Het
Cyp8b1 A G 9: 121,915,618 V216A probably benign Het
Dnah8 C T 17: 30,854,937 T4527M probably damaging Het
Elavl3 A G 9: 22,018,744 V288A probably damaging Het
Erap1 T A 13: 74,668,028 L92Q probably damaging Het
Exoc3l G T 8: 105,293,405 P296H probably damaging Het
Gm5294 A T 5: 138,820,968 N78Y probably damaging Het
Hacl1 T C 14: 31,634,191 probably benign Het
Hrnr T A 3: 93,322,855 N133K probably benign Het
Itgax G T 7: 128,136,273 R504S possibly damaging Het
Itgb4 A G 11: 116,005,926 S1461G possibly damaging Het
Klkb1 G T 8: 45,282,801 T175K probably damaging Het
Lrrk2 A T 15: 91,712,780 D525V possibly damaging Het
Lrrk2 C A 15: 91,778,504 T1912K probably damaging Het
Mdga1 G T 17: 29,857,622 Q59K probably damaging Het
Mpp4 A G 1: 59,124,683 V466A possibly damaging Het
Myh6 T C 14: 54,963,055 D203G probably benign Het
Myo5b T C 18: 74,716,037 S1116P probably damaging Het
Nemp1 T C 10: 127,695,473 L311P probably damaging Het
Nup205 A G 6: 35,219,742 R1138G probably damaging Het
Nup54 A G 5: 92,417,529 M443T probably damaging Het
Peak1 T C 9: 56,260,365 E93G probably benign Het
Pirb A T 7: 3,717,638 L287Q probably benign Het
Plekhj1 A G 10: 80,797,775 I76T probably damaging Het
Poll A G 19: 45,558,418 probably benign Het
Ppp1r3a A T 6: 14,719,074 S614T probably damaging Het
Pygm A T 19: 6,392,950 I556F probably benign Het
Ranbp2 T C 10: 58,476,472 F1005L probably benign Het
Rcor3 G T 1: 192,101,085 T361K possibly damaging Het
Robo4 A G 9: 37,402,017 probably benign Het
Rps15 T C 10: 80,293,839 V96A probably benign Het
Rrm2 T A 12: 24,709,432 N55K probably damaging Het
Shank2 T C 7: 144,128,375 Y382H probably benign Het
Slc25a10 G T 11: 120,491,993 E3* probably null Het
Slc7a8 T A 14: 54,735,841 E223V probably benign Het
Snx13 A G 12: 35,144,097 K880E probably benign Het
Spinkl T G 18: 44,168,149 M41L probably benign Het
Srp54a A C 12: 55,089,257 N19T probably benign Het
Sun2 T C 15: 79,734,155 K268E probably benign Het
Sytl1 G A 4: 133,255,624 Q359* probably null Het
Tlr6 A T 5: 64,953,595 F656L probably damaging Het
Tmem185a C T X: 70,462,186 probably null Het
Tmem45a2 C T 16: 57,039,035 D278N probably benign Het
Trav7-1 T C 14: 52,655,334 probably benign Het
Trpc2 T A 7: 102,093,574 M597K probably damaging Het
Ttc21a A G 9: 119,950,816 probably benign Het
Usp9y C T Y: 1,313,741 M2188I probably damaging Het
Utrn C A 10: 12,750,030 probably null Het
Zfp955b T A 17: 33,305,416 Y59F probably damaging Het
Other mutations in Vmn1r35
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00962:Vmn1r35 APN 6 66679377 missense possibly damaging 0.90
IGL01417:Vmn1r35 APN 6 66679207 missense probably benign 0.00
IGL01517:Vmn1r35 APN 6 66679450 missense probably benign 0.01
IGL02142:Vmn1r35 APN 6 66679350 missense probably damaging 1.00
IGL02178:Vmn1r35 APN 6 66679102 missense probably damaging 1.00
IGL02383:Vmn1r35 APN 6 66678891 missense probably damaging 1.00
IGL02383:Vmn1r35 APN 6 66678892 missense probably damaging 1.00
IGL02493:Vmn1r35 APN 6 66679479 missense possibly damaging 0.76
R0360:Vmn1r35 UTSW 6 66678843 missense probably damaging 0.99
R0364:Vmn1r35 UTSW 6 66678843 missense probably damaging 0.99
R0599:Vmn1r35 UTSW 6 66679513 missense probably benign 0.06
R1447:Vmn1r35 UTSW 6 66678906 missense probably benign 0.13
R1781:Vmn1r35 UTSW 6 66679566 missense probably benign 0.24
R2096:Vmn1r35 UTSW 6 66678945 missense possibly damaging 0.94
R2937:Vmn1r35 UTSW 6 66678966 missense possibly damaging 0.78
R2938:Vmn1r35 UTSW 6 66678966 missense possibly damaging 0.78
R3937:Vmn1r35 UTSW 6 66679073 missense probably damaging 1.00
R4386:Vmn1r35 UTSW 6 66679589 nonsense probably null
R5329:Vmn1r35 UTSW 6 66679506 nonsense probably null
R6638:Vmn1r35 UTSW 6 66678864 missense possibly damaging 0.63
R7175:Vmn1r35 UTSW 6 66678922 missense probably benign 0.06
R7448:Vmn1r35 UTSW 6 66679235 start gained probably benign
R7825:Vmn1r35 UTSW 6 66679459 missense probably damaging 1.00
R9139:Vmn1r35 UTSW 6 66678949 missense probably benign 0.10
R9415:Vmn1r35 UTSW 6 66679131 missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- TGTAGGATAGGCATTCATCACAAAC -3'
(R):5'- AGGATCATCTATACTGGTGCTTATACC -3'

Sequencing Primer
(F):5'- GGATAGGCATTCATCACAAACTTCTG -3'
(R):5'- ACATCATCAGGGGACTGA -3'
Posted On 2015-04-17