Incidental Mutation 'IGL03199:Vmn1r209'
ID412918
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r209
Ensembl Gene ENSMUSG00000071491
Gene Namevomeronasal 1 receptor 209
SynonymsGm11315
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.111) question?
Stock #IGL03199
Quality Score
Status
Chromosome13
Chromosomal Location22800629-22809682 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 22806050 bp
ZygosityHeterozygous
Amino Acid Change Serine to Threonine at position 157 (S157T)
Ref Sequence ENSEMBL: ENSMUSP00000153997 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095961] [ENSMUST00000227038] [ENSMUST00000227265]
Predicted Effect possibly damaging
Transcript: ENSMUST00000095961
AA Change: S157T

PolyPhen 2 Score 0.888 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000093657
Gene: ENSMUSG00000071491
AA Change: S157T

DomainStartEndE-ValueType
Pfam:TAS2R 2 294 9.8e-9 PFAM
Pfam:V1R 34 297 3e-36 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000227038
AA Change: S157T

PolyPhen 2 Score 0.888 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227265
AA Change: S157T

PolyPhen 2 Score 0.888 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930407I10Rik T C 15: 82,062,355 I151T possibly damaging Het
9030624J02Rik T C 7: 118,766,388 S15P probably benign Het
Alms1 T A 6: 85,622,497 M1904K possibly damaging Het
Chsy3 T A 18: 59,176,401 F242Y probably damaging Het
Cwf19l2 G A 9: 3,477,830 G845D probably damaging Het
Cyfip2 A G 11: 46,276,843 I244T probably benign Het
Dnah10 A T 5: 124,817,697 Q3499L probably benign Het
Fat3 A G 9: 16,377,048 V393A possibly damaging Het
Fcamr T A 1: 130,812,918 V358D probably damaging Het
Fndc3c1 T A X: 106,436,387 K696N possibly damaging Het
Igkv2-112 G A 6: 68,220,016 M12I probably benign Het
Macc1 T C 12: 119,446,421 M308T probably benign Het
Map4k1 A G 7: 28,983,417 E16G probably damaging Het
Myl7 C T 11: 5,898,205 G50R probably damaging Het
Ncapg2 T A 12: 116,419,236 L229H probably damaging Het
Olfr960 A G 9: 39,623,944 I272V probably benign Het
Prkcz A G 4: 155,272,984 F157L possibly damaging Het
Sult2a1 C A 7: 13,832,660 G130V probably damaging Het
Trim27 G A 13: 21,191,251 probably null Het
Trim43b T G 9: 89,089,428 Q225P probably damaging Het
Ugt2b34 A G 5: 86,906,880 L14P unknown Het
Vmn2r38 A T 7: 9,075,376 V669D probably damaging Het
Zfp422 T C 6: 116,626,951 Q29R probably benign Het
Zfp623 C T 15: 75,947,270 A25V probably benign Het
Other mutations in Vmn1r209
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01773:Vmn1r209 APN 13 22806280 missense probably damaging 1.00
IGL01788:Vmn1r209 APN 13 22805662 missense probably damaging 0.97
IGL02738:Vmn1r209 APN 13 22806120 nonsense probably null
IGL03177:Vmn1r209 APN 13 22805854 missense possibly damaging 0.46
R0437:Vmn1r209 UTSW 13 22806356 missense probably benign 0.01
R0497:Vmn1r209 UTSW 13 22805948 missense probably damaging 1.00
R0506:Vmn1r209 UTSW 13 22805944 missense probably damaging 0.98
R1496:Vmn1r209 UTSW 13 22805764 missense probably damaging 1.00
R1644:Vmn1r209 UTSW 13 22806482 missense possibly damaging 0.52
R1829:Vmn1r209 UTSW 13 22806239 missense possibly damaging 0.95
R2360:Vmn1r209 UTSW 13 22805666 missense probably damaging 1.00
R3434:Vmn1r209 UTSW 13 22806097 missense probably benign 0.04
R3435:Vmn1r209 UTSW 13 22806097 missense probably benign 0.04
R4082:Vmn1r209 UTSW 13 22805615 missense probably null 0.15
R4451:Vmn1r209 UTSW 13 22806498 missense probably benign 0.02
R4616:Vmn1r209 UTSW 13 22805965 missense probably damaging 1.00
R4618:Vmn1r209 UTSW 13 22806449 missense possibly damaging 0.87
R4801:Vmn1r209 UTSW 13 22805656 missense probably damaging 1.00
R4802:Vmn1r209 UTSW 13 22805656 missense probably damaging 1.00
R6035:Vmn1r209 UTSW 13 22806032 missense probably benign 0.02
R6035:Vmn1r209 UTSW 13 22806032 missense probably benign 0.02
R6908:Vmn1r209 UTSW 13 22806230 missense possibly damaging 0.60
R7162:Vmn1r209 UTSW 13 22805958 missense probably damaging 1.00
R7772:Vmn1r209 UTSW 13 22806494 missense possibly damaging 0.77
R8328:Vmn1r209 UTSW 13 22806473 missense probably benign 0.00
R8335:Vmn1r209 UTSW 13 22805807 missense probably damaging 1.00
Posted On2016-08-02