Incidental Mutation 'IGL01673:Vmn1r74'
ID 103554
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r74
Ensembl Gene ENSMUSG00000047655
Gene Name vomeronasal 1 receptor 74
Synonyms V1rg5
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # IGL01673
Quality Score
Status
Chromosome 7
Chromosomal Location 11580702-11581616 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 11581317 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 206 (I206F)
Ref Sequence ENSEMBL: ENSMUSP00000154746 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050416] [ENSMUST00000228471]
AlphaFold Q8R290
Predicted Effect possibly damaging
Transcript: ENSMUST00000050416
AA Change: I206F

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000055148
Gene: ENSMUSG00000047655
AA Change: I206F

DomainStartEndE-ValueType
Pfam:7tm_1 22 290 1.3e-7 PFAM
Pfam:V1R 34 296 1.2e-31 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210930
Predicted Effect possibly damaging
Transcript: ENSMUST00000228471
AA Change: I206F

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cpz A T 5: 35,669,891 (GRCm39) V262E probably benign Het
Cyp4f14 A G 17: 33,130,125 (GRCm39) probably null Het
Ddx46 G T 13: 55,800,861 (GRCm39) V339F probably damaging Het
Gpn1 T G 5: 31,652,179 (GRCm39) C21W probably damaging Het
Gpr63 A T 4: 25,008,014 (GRCm39) Q246L probably benign Het
Hsp90b1 T A 10: 86,529,296 (GRCm39) M658L probably damaging Het
Immp2l T C 12: 41,118,320 (GRCm39) S4P probably benign Het
Krtap9-5 A T 11: 99,840,377 (GRCm39) *359C probably null Het
Lgals7 A G 7: 28,565,621 (GRCm39) probably benign Het
Mak G T 13: 41,201,699 (GRCm39) probably null Het
Mrps18c A G 5: 100,946,672 (GRCm39) R13G possibly damaging Het
Myo7a A G 7: 97,703,915 (GRCm39) V1946A probably benign Het
Nfyc T C 4: 120,636,307 (GRCm39) probably benign Het
Nkx2-4 C T 2: 146,925,834 (GRCm39) V343M possibly damaging Het
Or5be3 T C 2: 86,863,731 (GRCm39) Y278C probably damaging Het
Or8d2 T C 9: 38,760,316 (GRCm39) V302A probably benign Het
Rapgef4 G T 2: 72,071,781 (GRCm39) S743I probably damaging Het
Tcf7 A G 11: 52,147,823 (GRCm39) C210R probably damaging Het
Ubqln3 T A 7: 103,791,605 (GRCm39) I162F probably benign Het
Vmn1r216 A G 13: 23,283,641 (GRCm39) Q108R probably damaging Het
Wdr64 T C 1: 175,627,922 (GRCm39) I872T possibly damaging Het
Other mutations in Vmn1r74
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01608:Vmn1r74 APN 7 11,581,560 (GRCm39) missense probably damaging 0.98
IGL03023:Vmn1r74 APN 7 11,581,257 (GRCm39) missense possibly damaging 0.46
IGL03409:Vmn1r74 APN 7 11,581,240 (GRCm39) missense probably damaging 0.99
R0393:Vmn1r74 UTSW 7 11,581,242 (GRCm39) missense possibly damaging 0.79
R1488:Vmn1r74 UTSW 7 11,581,510 (GRCm39) missense probably benign 0.02
R1707:Vmn1r74 UTSW 7 11,581,504 (GRCm39) missense probably damaging 0.98
R1998:Vmn1r74 UTSW 7 11,581,302 (GRCm39) missense probably damaging 1.00
R1999:Vmn1r74 UTSW 7 11,581,302 (GRCm39) missense probably damaging 1.00
R2139:Vmn1r74 UTSW 7 11,581,243 (GRCm39) missense probably damaging 1.00
R4027:Vmn1r74 UTSW 7 11,580,898 (GRCm39) missense probably damaging 0.98
R4576:Vmn1r74 UTSW 7 11,580,696 (GRCm39) splice site probably null
R4619:Vmn1r74 UTSW 7 11,581,403 (GRCm39) missense probably damaging 1.00
R4619:Vmn1r74 UTSW 7 11,581,398 (GRCm39) missense possibly damaging 0.61
R5371:Vmn1r74 UTSW 7 11,580,984 (GRCm39) missense probably damaging 1.00
R5606:Vmn1r74 UTSW 7 11,580,822 (GRCm39) missense probably benign 0.01
R6464:Vmn1r74 UTSW 7 11,581,131 (GRCm39) missense possibly damaging 0.87
R6901:Vmn1r74 UTSW 7 11,581,368 (GRCm39) missense probably benign 0.00
R6920:Vmn1r74 UTSW 7 11,581,575 (GRCm39) missense probably benign 0.01
R7223:Vmn1r74 UTSW 7 11,580,894 (GRCm39) nonsense probably null
R7231:Vmn1r74 UTSW 7 11,580,888 (GRCm39) missense probably benign 0.34
R7418:Vmn1r74 UTSW 7 11,581,081 (GRCm39) missense possibly damaging 0.88
R8135:Vmn1r74 UTSW 7 11,581,530 (GRCm39) missense probably benign 0.36
R8692:Vmn1r74 UTSW 7 11,580,972 (GRCm39) missense probably benign 0.03
R8748:Vmn1r74 UTSW 7 11,580,903 (GRCm39) missense probably benign 0.10
R9004:Vmn1r74 UTSW 7 11,580,840 (GRCm39) missense probably benign 0.00
R9258:Vmn1r74 UTSW 7 11,580,999 (GRCm39) missense possibly damaging 0.86
R9564:Vmn1r74 UTSW 7 11,581,534 (GRCm39) missense probably damaging 1.00
RF049:Vmn1r74 UTSW 7 11,581,067 (GRCm39) frame shift probably null
RF063:Vmn1r74 UTSW 7 11,581,067 (GRCm39) frame shift probably null
Z1176:Vmn1r74 UTSW 7 11,580,936 (GRCm39) missense probably benign
Posted On 2014-01-21