Incidental Mutation 'IGL02610:Vmn1r7'
ID300455
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r7
Ensembl Gene ENSMUSG00000093696
Gene Namevomeronasal 1 receptor 7
SynonymsGm5568, V1rc31
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.163) question?
Stock #IGL02610
Quality Score
Status
Chromosome6
Chromosomal Location57024106-57025324 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 57025052 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Leucine at position 74 (F74L)
Ref Sequence ENSEMBL: ENSMUSP00000135571 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176252]
Predicted Effect probably benign
Transcript: ENSMUST00000176252
AA Change: F74L

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000135571
Gene: ENSMUSG00000093696
AA Change: F74L

DomainStartEndE-ValueType
Pfam:V1R 28 293 1.1e-59 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Armc8 T C 9: 99,527,069 probably benign Het
Ccdc93 T G 1: 121,492,971 V527G probably benign Het
Ctcfl C A 2: 173,106,026 probably benign Het
Dmd T C X: 83,664,156 S359P probably damaging Het
Drc3 T C 11: 60,370,593 F190S probably benign Het
Dync1h1 A T 12: 110,659,232 K3943* probably null Het
Dzip3 A G 16: 48,951,653 V551A probably damaging Het
Ep300 T A 15: 81,601,522 L237M unknown Het
Gab1 A G 8: 80,800,099 probably null Het
Gm6430 G A 1: 97,024,835 noncoding transcript Het
Gm8765 T C 13: 50,701,712 V462A possibly damaging Het
Ighv16-1 A T 12: 114,069,113 V23E probably damaging Het
Ikbkb T A 8: 22,675,072 probably null Het
Ncr1 A T 7: 4,338,133 N41I probably benign Het
Nfkbib T C 7: 28,759,849 D319G probably damaging Het
Nkain3 T C 4: 20,469,459 E85G probably damaging Het
Olfr555 G A 7: 102,659,567 V249M probably benign Het
Pip5k1c C A 10: 81,317,321 probably null Het
Ppp2r2b A G 18: 42,648,775 probably benign Het
Rgs11 G A 17: 26,207,631 V279I probably benign Het
Rhod A G 19: 4,426,175 F183L probably damaging Het
Slc35f3 A T 8: 126,321,217 T99S probably damaging Het
Spock3 A G 8: 63,345,737 Y264C probably damaging Het
Trnt1 T C 6: 106,778,818 F278S possibly damaging Het
Ush2a T A 1: 188,444,466 Y1276N probably damaging Het
Veph1 A G 3: 66,172,167 L309P probably damaging Het
Vsnl1 C T 12: 11,332,071 W103* probably null Het
Other mutations in Vmn1r7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01382:Vmn1r7 APN 6 57024723 missense probably damaging 1.00
IGL01528:Vmn1r7 APN 6 57024547 missense probably benign
IGL02024:Vmn1r7 APN 6 57024889 missense probably benign 0.01
IGL02234:Vmn1r7 APN 6 57024552 missense probably damaging 0.98
IGL02691:Vmn1r7 APN 6 57024388 missense probably benign 0.05
R0529:Vmn1r7 UTSW 6 57024465 missense possibly damaging 0.78
R0548:Vmn1r7 UTSW 6 57025081 missense probably damaging 0.96
R1254:Vmn1r7 UTSW 6 57024787 missense probably damaging 1.00
R1279:Vmn1r7 UTSW 6 57024949 missense possibly damaging 0.63
R1582:Vmn1r7 UTSW 6 57025158 missense probably damaging 1.00
R1973:Vmn1r7 UTSW 6 57025026 missense probably benign 0.00
R1991:Vmn1r7 UTSW 6 57024868 missense probably benign 0.37
R2160:Vmn1r7 UTSW 6 57024894 missense probably damaging 0.97
R3546:Vmn1r7 UTSW 6 57024849 missense possibly damaging 0.80
R3547:Vmn1r7 UTSW 6 57024849 missense possibly damaging 0.80
R5901:Vmn1r7 UTSW 6 57024606 missense probably damaging 1.00
R6294:Vmn1r7 UTSW 6 57024419 missense probably benign 0.00
R7063:Vmn1r7 UTSW 6 57024433 missense possibly damaging 0.63
R7192:Vmn1r7 UTSW 6 57024467 missense probably benign 0.00
R7647:Vmn1r7 UTSW 6 57025270 missense probably benign 0.01
R7781:Vmn1r7 UTSW 6 57024568 missense probably benign 0.03
Posted On2015-04-16