Incidental Mutation 'R6336:Vmn2r30'
ID510758
Institutional Source Beutler Lab
Gene Symbol Vmn2r30
Ensembl Gene ENSMUSG00000070847
Gene Namevomeronasal 2, receptor 30
SynonymsV2r15
MMRRC Submission
Accession Numbers
Is this an essential gene? Not available question?
Stock #R6336 (G1)
Quality Score220.009
Status Not validated
Chromosome7
Chromosomal Location7311333-7337609 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 7334308 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Serine at position 110 (T110S)
Ref Sequence ENSEMBL: ENSMUSP00000134223 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072475] [ENSMUST00000174368] [ENSMUST00000210877]
Predicted Effect probably benign
Transcript: ENSMUST00000072475
AA Change: T110S

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000072296
Gene: ENSMUSG00000070847
AA Change: T110S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 160 469 2.1e-25 PFAM
Pfam:NCD3G 512 565 8.1e-21 PFAM
Pfam:7tm_3 598 833 2.1e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174368
AA Change: T110S

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000134223
Gene: ENSMUSG00000070847
AA Change: T110S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 155 468 1.5e-27 PFAM
Pfam:NCD3G 512 564 7.2e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210877
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.0%
Validation Efficiency 98% (45/46)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900026A02Rik G T 5: 113,183,483 P955Q possibly damaging Het
Adgrv1 T C 13: 81,385,981 N5827S probably benign Het
Akt3 T C 1: 177,031,712 D431G probably damaging Het
Anapc16 A T 10: 59,988,829 V76D possibly damaging Het
Ankib1 A T 5: 3,700,377 Y755* probably null Het
Ankrd6 A G 4: 32,860,411 S11P probably damaging Het
Card6 T A 15: 5,099,164 K917* probably null Het
Ccdc152 T C 15: 3,301,129 I21M probably damaging Het
Ccdc40 A G 11: 119,231,993 E207G possibly damaging Het
Clca3a2 G T 3: 144,806,478 A499E probably benign Het
Cntnap5b C T 1: 100,358,669 A383V probably benign Het
Ddo T C 10: 40,633,031 V89A probably damaging Het
Depdc5 T C 5: 32,964,507 probably null Het
Dlgap1 T A 17: 70,815,289 D904E probably damaging Het
Ephb4 T A 5: 137,372,085 L849H probably damaging Het
Fbxl13 A G 5: 21,523,547 probably null Het
Fer1l6 C A 15: 58,559,232 Y245* probably null Het
Foxred2 A G 15: 77,955,764 Y109H probably damaging Het
Gabarapl1 A G 6: 129,537,528 D43G probably benign Het
Gabrb1 A C 5: 72,029,898 E178A possibly damaging Het
Gbp11 A G 5: 105,325,489 Het
Gm31371 A G 8: 19,924,350 K242E unknown Het
Grin3b C A 10: 79,976,461 A845E probably damaging Het
Hoxd4 A G 2: 74,727,361 Y28C probably damaging Het
Igsf10 G A 3: 59,330,339 T807M probably benign Het
Kcnt1 A G 2: 25,888,755 probably null Het
Kdm5a C A 6: 120,398,978 T565K probably damaging Het
Map7d1 A G 4: 126,236,682 S412P probably damaging Het
Mok A G 12: 110,834,124 probably null Het
Mto1 A T 9: 78,473,835 I73F probably damaging Het
Mtss1l G A 8: 110,732,164 D310N probably damaging Het
Ncf2 T C 1: 152,834,070 Y393H probably damaging Het
Olfr1299 A G 2: 111,664,619 H131R possibly damaging Het
Olfr1317 A C 2: 112,142,406 I154L probably benign Het
Olfr1384 G T 11: 49,514,542 K301N probably damaging Het
Olfr272 A T 4: 52,911,459 C112S probably damaging Het
Olfr38 T C 6: 42,762,657 S202P probably damaging Het
Olfr67 T C 7: 103,788,245 T11A possibly damaging Het
Phxr2 T A 10: 99,126,090 probably benign Het
Rnf17 A G 14: 56,421,169 probably null Het
Serpinb9d T C 13: 33,194,694 M41T probably damaging Het
Slc12a5 T A 2: 164,992,464 probably null Het
Slc22a6 G A 19: 8,622,130 R331H probably benign Het
Spg11 G C 2: 122,112,959 probably null Het
Src T A 2: 157,457,155 V24E probably benign Het
Srgap1 A T 10: 121,925,941 Y101N probably benign Het
Vwa3a A G 7: 120,762,423 E119G possibly damaging Het
Whamm T A 7: 81,591,764 D274E probably damaging Het
Other mutations in Vmn2r30
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01797:Vmn2r30 APN 7 7334196 missense probably benign
IGL02114:Vmn2r30 APN 7 7337409 missense possibly damaging 0.62
IGL02429:Vmn2r30 APN 7 7334244 missense possibly damaging 0.95
IGL03214:Vmn2r30 APN 7 7334260 missense probably benign 0.00
R1723:Vmn2r30 UTSW 7 7334260 missense probably benign 0.00
R4472:Vmn2r30 UTSW 7 7317092 missense probably damaging 1.00
R5409:Vmn2r30 UTSW 7 7312548 missense probably damaging 1.00
R5979:Vmn2r30 UTSW 7 7312335 missense probably damaging 0.99
R6035:Vmn2r30 UTSW 7 7334351 missense probably benign 0.34
R6035:Vmn2r30 UTSW 7 7334351 missense probably benign 0.34
R6904:Vmn2r30 UTSW 7 7312548 missense probably damaging 1.00
R7124:Vmn2r30 UTSW 7 7334184 missense probably benign 0.05
V8831:Vmn2r30 UTSW 7 7334149 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AACTCACACGCGGAGATAAG -3'
(R):5'- ATGTCAGATGCAGAAACTTCCAG -3'

Sequencing Primer
(F):5'- GAAGCTGTCCAGGTACATCCAG -3'
(R):5'- CAGATGCAGAAACTTCCAGTATAGTG -3'
Posted On2018-04-02