Incidental Mutation 'R4408:Vmn2r33'
ID 327760
Institutional Source Beutler Lab
Gene Symbol Vmn2r33
Ensembl Gene ENSMUSG00000096691
Gene Name vomeronasal 2, receptor 33
Synonyms
MMRRC Submission 041690-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4408 (G1)
Quality Score 173
Status Not validated
Chromosome 7
Chromosomal Location 7553966-7569785 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 7554229 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Valine at position 775 (F775V)
Ref Sequence ENSEMBL: ENSMUSP00000129960 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165921]
AlphaFold K7N705
Predicted Effect probably damaging
Transcript: ENSMUST00000165921
AA Change: F775V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129960
Gene: ENSMUSG00000096691
AA Change: F775V

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 4.2e-34 PFAM
Pfam:NCD3G 512 565 4.1e-19 PFAM
Pfam:7tm_3 598 833 3.1e-55 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency 97% (35/36)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cacna1h A G 17: 25,599,601 (GRCm39) V1588A probably damaging Het
Card6 T A 15: 5,130,536 (GRCm39) M287L probably damaging Het
Fam227b T A 2: 125,958,045 (GRCm39) Y240F possibly damaging Het
Fbln1 T A 15: 85,115,757 (GRCm39) probably null Het
Fndc5 A G 4: 129,036,322 (GRCm39) probably null Het
Gm10799 C A 2: 103,898,409 (GRCm39) A99S possibly damaging Het
Gm27013 A T 6: 130,654,728 (GRCm39) S245T possibly damaging Het
Gm5592 A G 7: 40,935,872 (GRCm39) T125A probably benign Het
Gml2 T C 15: 74,696,188 (GRCm39) probably benign Het
Gpbp1 A T 13: 111,585,498 (GRCm39) N149K possibly damaging Het
Gprc6a T C 10: 51,504,639 (GRCm39) I68M probably benign Het
Hnrnpu T C 1: 178,158,368 (GRCm39) probably benign Het
Irf5 A G 6: 29,534,000 (GRCm39) probably null Het
Lrp2 T A 2: 69,297,513 (GRCm39) K3149N probably benign Het
Lrrn3 A G 12: 41,504,041 (GRCm39) V92A probably benign Het
Map3k12 T C 15: 102,413,837 (GRCm39) T45A probably damaging Het
Myof A G 19: 37,911,426 (GRCm39) S1502P probably damaging Het
Or4k77 T A 2: 111,199,625 (GRCm39) I216K possibly damaging Het
Or9s18 A G 13: 65,300,514 (GRCm39) T159A probably benign Het
Osr2 T C 15: 35,300,617 (GRCm39) Y58H possibly damaging Het
Pop5 C T 5: 115,378,836 (GRCm39) probably benign Het
Ror2 A G 13: 53,272,997 (GRCm39) C211R probably damaging Het
Rufy4 T C 1: 74,186,822 (GRCm39) C537R probably damaging Het
Sgsm2 C A 11: 74,742,592 (GRCm39) R957L probably damaging Het
Slc16a11 A G 11: 70,106,560 (GRCm39) probably null Het
Spag17 T A 3: 100,010,694 (GRCm39) Y2063N probably benign Het
Usp25 A C 16: 76,912,341 (GRCm39) K1020T probably damaging Het
Vmn1r23 T C 6: 57,903,353 (GRCm39) I142V probably benign Het
Vmn1r235 A G 17: 21,481,854 (GRCm39) K60E probably damaging Het
Vps13b C T 15: 35,709,440 (GRCm39) P1796S probably damaging Het
Vwa3a G A 7: 120,378,149 (GRCm39) V480I probably benign Het
Other mutations in Vmn2r33
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01893:Vmn2r33 APN 7 7,566,776 (GRCm39) missense probably benign
R1147:Vmn2r33 UTSW 7 7,557,144 (GRCm39) missense probably benign 0.16
R1147:Vmn2r33 UTSW 7 7,557,144 (GRCm39) missense probably benign 0.16
R3966:Vmn2r33 UTSW 7 7,557,168 (GRCm39) missense probably benign 0.00
R6571:Vmn2r33 UTSW 7 7,566,668 (GRCm39) missense probably benign 0.00
R6783:Vmn2r33 UTSW 7 7,566,797 (GRCm39) missense probably benign
R7180:Vmn2r33 UTSW 7 7,566,896 (GRCm39) missense probably benign 0.00
R7984:Vmn2r33 UTSW 7 7,566,862 (GRCm39) missense probably benign 0.01
R8202:Vmn2r33 UTSW 7 7,557,153 (GRCm39) missense possibly damaging 0.87
R8894:Vmn2r33 UTSW 7 7,566,809 (GRCm39) missense probably benign 0.00
R8954:Vmn2r33 UTSW 7 7,554,655 (GRCm39) missense probably benign 0.02
R8995:Vmn2r33 UTSW 7 7,554,192 (GRCm39) missense probably damaging 1.00
R9027:Vmn2r33 UTSW 7 7,554,168 (GRCm39) missense probably damaging 1.00
R9564:Vmn2r33 UTSW 7 7,557,081 (GRCm39) missense probably benign 0.06
R9608:Vmn2r33 UTSW 7 7,557,153 (GRCm39) missense possibly damaging 0.87
Predicted Primers PCR Primer
(F):5'- CCAACTTTACATTGGACACAATTCC -3'
(R):5'- GGCTAGAAGTTTCTCCTCCC -3'

Sequencing Primer
(F):5'- GGACACAATTCCTGAATTATTCGTTC -3'
(R):5'- CTCCCTTTGTTGATATTGATGAACAC -3'
Posted On 2015-07-07