Incidental Mutation 'IGL01504:Vmn1r177'
ID 88992
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r177
Ensembl Gene ENSMUSG00000057513
Gene Name vomeronasal 1 receptor 177
Synonyms V1rd12
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL01504
Quality Score
Status
Chromosome 7
Chromosomal Location 23564945-23565874 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 23565835 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Methionine at position 14 (V14M)
Ref Sequence ENSEMBL: ENSMUSP00000073621 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073967]
AlphaFold E9PXM3
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: 87,284,231 (GRCm39) I326N probably damaging Het
Acot6 G A 12: 84,156,176 (GRCm39) V375M probably benign Het
Als2cl G A 9: 110,718,351 (GRCm39) R364Q probably benign Het
Cpa1 A T 6: 30,640,720 (GRCm39) T121S probably benign Het
Ctnnbl1 A G 2: 157,660,036 (GRCm39) probably benign Het
Frrs1 C A 3: 116,694,307 (GRCm39) Q76K probably damaging Het
Gja10 T A 4: 32,602,375 (GRCm39) D3V probably damaging Het
Insyn2a T A 7: 134,519,669 (GRCm39) Q287L probably benign Het
Krt76 T C 15: 101,796,608 (GRCm39) E400G probably damaging Het
Mdm1 A G 10: 117,982,505 (GRCm39) T47A probably damaging Het
Ncf2 A G 1: 152,709,080 (GRCm39) K336R probably benign Het
Ndrg4 C A 8: 96,432,894 (GRCm39) L34I probably damaging Het
Phf20l1 T A 15: 66,469,540 (GRCm39) H148Q possibly damaging Het
Rhobtb1 A G 10: 69,085,528 (GRCm39) H89R probably damaging Het
Sult1e1 T C 5: 87,724,160 (GRCm39) N266D probably damaging Het
Sult2a2 T C 7: 13,472,189 (GRCm39) S129P probably damaging Het
Trank1 A G 9: 111,202,612 (GRCm39) E1659G probably damaging Het
Trpa1 T G 1: 14,952,443 (GRCm39) I863L possibly damaging Het
Vmn2r14 A T 5: 109,369,285 (GRCm39) M96K probably benign Het
Zp1 C T 19: 10,896,375 (GRCm39) V117M probably damaging Het
Other mutations in Vmn1r177
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01456:Vmn1r177 APN 7 23,565,753 (GRCm39) missense possibly damaging 0.58
IGL01535:Vmn1r177 APN 7 23,565,765 (GRCm39) missense probably damaging 1.00
IGL01551:Vmn1r177 APN 7 23,565,688 (GRCm39) missense probably benign 0.04
IGL01647:Vmn1r177 APN 7 23,565,600 (GRCm39) missense probably damaging 1.00
ANU74:Vmn1r177 UTSW 7 23,565,645 (GRCm39) missense possibly damaging 0.86
R0396:Vmn1r177 UTSW 7 23,565,022 (GRCm39) missense probably damaging 1.00
R0894:Vmn1r177 UTSW 7 23,565,475 (GRCm39) missense probably benign 0.09
R1446:Vmn1r177 UTSW 7 23,565,765 (GRCm39) missense probably damaging 1.00
R1835:Vmn1r177 UTSW 7 23,565,111 (GRCm39) missense probably damaging 1.00
R1893:Vmn1r177 UTSW 7 23,565,573 (GRCm39) missense probably benign 0.02
R1995:Vmn1r177 UTSW 7 23,565,112 (GRCm39) missense probably damaging 1.00
R2206:Vmn1r177 UTSW 7 23,565,556 (GRCm39) missense probably damaging 1.00
R3889:Vmn1r177 UTSW 7 23,565,289 (GRCm39) missense possibly damaging 0.86
R4458:Vmn1r177 UTSW 7 23,565,645 (GRCm39) missense possibly damaging 0.86
R4579:Vmn1r177 UTSW 7 23,565,772 (GRCm39) missense possibly damaging 0.46
R5290:Vmn1r177 UTSW 7 23,565,498 (GRCm39) missense probably damaging 0.99
R6128:Vmn1r177 UTSW 7 23,565,268 (GRCm39) missense probably damaging 1.00
R6128:Vmn1r177 UTSW 7 23,565,267 (GRCm39) missense probably damaging 0.99
R6730:Vmn1r177 UTSW 7 23,565,237 (GRCm39) missense probably damaging 1.00
R6785:Vmn1r177 UTSW 7 23,565,562 (GRCm39) missense probably damaging 1.00
R7100:Vmn1r177 UTSW 7 23,565,535 (GRCm39) missense probably benign 0.15
R7738:Vmn1r177 UTSW 7 23,565,559 (GRCm39) missense probably damaging 1.00
R8191:Vmn1r177 UTSW 7 23,565,736 (GRCm39) nonsense probably null
R8980:Vmn1r177 UTSW 7 23,565,144 (GRCm39) missense probably damaging 1.00
R9723:Vmn1r177 UTSW 7 23,565,774 (GRCm39) missense probably damaging 0.97
R9771:Vmn1r177 UTSW 7 23,565,657 (GRCm39) missense probably damaging 0.98
X0020:Vmn1r177 UTSW 7 23,565,718 (GRCm39) missense probably damaging 1.00
Z1177:Vmn1r177 UTSW 7 23,565,360 (GRCm39) missense probably damaging 0.99
Posted On 2013-12-03