Incidental Mutation 'IGL01504:Vmn1r177'
ID88992
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r177
Ensembl Gene ENSMUSG00000057513
Gene Namevomeronasal 1 receptor 177
SynonymsV1rd12
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.086) question?
Stock #IGL01504
Quality Score
Status
Chromosome7
Chromosomal Location23865520-23866449 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 23866410 bp
ZygosityHeterozygous
Amino Acid Change Valine to Methionine at position 14 (V14M)
Ref Sequence ENSEMBL: ENSMUSP00000073621 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073967]
Predicted Effect probably damaging
Transcript: ENSMUST00000073967
AA Change: V14M

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000073621
Gene: ENSMUSG00000057513
AA Change: V14M

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 4.1e-13 PFAM
Pfam:V1R 41 297 5.3e-14 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207027
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc12 A T 8: 86,557,602 I326N probably damaging Het
Acot6 G A 12: 84,109,402 V375M probably benign Het
Als2cl G A 9: 110,889,283 R364Q probably benign Het
Cpa1 A T 6: 30,640,721 T121S probably benign Het
Ctnnbl1 A G 2: 157,818,116 probably benign Het
Fam196a T A 7: 134,917,940 Q287L probably benign Het
Frrs1 C A 3: 116,900,658 Q76K probably damaging Het
Gja10 T A 4: 32,602,375 D3V probably damaging Het
Krt76 T C 15: 101,888,173 E400G probably damaging Het
Mdm1 A G 10: 118,146,600 T47A probably damaging Het
Ncf2 A G 1: 152,833,329 K336R probably benign Het
Ndrg4 C A 8: 95,706,266 L34I probably damaging Het
Phf20l1 T A 15: 66,597,691 H148Q possibly damaging Het
Rhobtb1 A G 10: 69,249,698 H89R probably damaging Het
Sult1e1 T C 5: 87,576,301 N266D probably damaging Het
Sult2a2 T C 7: 13,738,264 S129P probably damaging Het
Trank1 A G 9: 111,373,544 E1659G probably damaging Het
Trpa1 T G 1: 14,882,219 I863L possibly damaging Het
Vmn2r14 A T 5: 109,221,419 M96K probably benign Het
Zp1 C T 19: 10,919,011 V117M probably damaging Het
Other mutations in Vmn1r177
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01456:Vmn1r177 APN 7 23866328 missense possibly damaging 0.58
IGL01535:Vmn1r177 APN 7 23866340 missense probably damaging 1.00
IGL01551:Vmn1r177 APN 7 23866263 missense probably benign 0.04
IGL01647:Vmn1r177 APN 7 23866175 missense probably damaging 1.00
ANU74:Vmn1r177 UTSW 7 23866220 missense possibly damaging 0.86
R0396:Vmn1r177 UTSW 7 23865597 missense probably damaging 1.00
R0894:Vmn1r177 UTSW 7 23866050 missense probably benign 0.09
R1446:Vmn1r177 UTSW 7 23866340 missense probably damaging 1.00
R1835:Vmn1r177 UTSW 7 23865686 missense probably damaging 1.00
R1893:Vmn1r177 UTSW 7 23866148 missense probably benign 0.02
R1995:Vmn1r177 UTSW 7 23865687 missense probably damaging 1.00
R2206:Vmn1r177 UTSW 7 23866131 missense probably damaging 1.00
R3889:Vmn1r177 UTSW 7 23865864 missense possibly damaging 0.86
R4458:Vmn1r177 UTSW 7 23866220 missense possibly damaging 0.86
R4579:Vmn1r177 UTSW 7 23866347 missense possibly damaging 0.46
R5290:Vmn1r177 UTSW 7 23866073 missense probably damaging 0.99
R6128:Vmn1r177 UTSW 7 23865842 missense probably damaging 0.99
R6128:Vmn1r177 UTSW 7 23865843 missense probably damaging 1.00
R6730:Vmn1r177 UTSW 7 23865812 missense probably damaging 1.00
R6785:Vmn1r177 UTSW 7 23866137 missense probably damaging 1.00
R7100:Vmn1r177 UTSW 7 23866110 missense probably benign 0.15
R7738:Vmn1r177 UTSW 7 23866134 missense probably damaging 1.00
R8191:Vmn1r177 UTSW 7 23866311 nonsense probably null
X0020:Vmn1r177 UTSW 7 23866293 missense probably damaging 1.00
Z1177:Vmn1r177 UTSW 7 23865935 missense probably damaging 0.99
Posted On2013-12-03