Incidental Mutation 'IGL01551:Vmn1r177'
ID 93256
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 # IGL01551
Quality Score
Status
Chromosome 7
Chromosomal Location 23564945-23565874 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 23565688 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 63 (I63V)
Ref Sequence ENSEMBL: ENSMUSP00000073621 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073967]
AlphaFold E9PXM3
Predicted Effect probably benign
Transcript: ENSMUST00000073967
AA Change: I63V

PolyPhen 2 Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000073621
Gene: ENSMUSG00000057513
AA Change: I63V

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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610008E11Rik G A 10: 78,924,147 (GRCm39) S103L possibly damaging Het
Acvr2a G A 2: 48,787,071 (GRCm39) A389T probably damaging Het
Adamts9 A G 6: 92,784,001 (GRCm39) S1037P probably damaging Het
Adcyap1 A G 17: 93,511,446 (GRCm39) Y140C probably damaging Het
Ampd3 A G 7: 110,404,183 (GRCm39) N569S probably damaging Het
Bin1 G T 18: 32,510,511 (GRCm39) V18L probably benign Het
Ccdc158 A G 5: 92,814,620 (GRCm39) Y69H probably damaging Het
Ccdc70 A G 8: 22,463,611 (GRCm39) R134G possibly damaging Het
Cmtm2a A G 8: 105,019,286 (GRCm39) V101A probably damaging Het
Edar T C 10: 58,441,860 (GRCm39) probably benign Het
Gcc2 T C 10: 58,134,691 (GRCm39) probably benign Het
Gm10961 A G 3: 107,540,281 (GRCm39) probably benign Het
Hsd3b3 T C 3: 98,649,216 (GRCm39) D369G probably benign Het
Ifi202b T A 1: 173,798,928 (GRCm39) K373N probably benign Het
Khk C A 5: 31,082,189 (GRCm39) H67N probably benign Het
Kif7 T A 7: 79,360,314 (GRCm39) probably null Het
Mbd1 C T 18: 74,402,614 (GRCm39) probably benign Het
Mtor A G 4: 148,556,494 (GRCm39) H968R probably damaging Het
Nadk A G 4: 155,673,157 (GRCm39) probably benign Het
Or11g27 A G 14: 50,771,618 (GRCm39) T250A probably benign Het
Or2f1b A G 6: 42,739,046 (GRCm39) D20G probably damaging Het
Or5d40 A T 2: 88,015,629 (GRCm39) H136L probably benign Het
Otol1 T C 3: 69,935,057 (GRCm39) F350L probably damaging Het
Pramel22 T C 4: 143,383,042 (GRCm39) N59S probably damaging Het
Prkcg G A 7: 3,352,342 (GRCm39) probably benign Het
Rps6kc1 A T 1: 190,505,837 (GRCm39) S1042T possibly damaging Het
Rtn1 C T 12: 72,263,709 (GRCm39) V741I possibly damaging Het
Tor2a T A 2: 32,650,595 (GRCm39) probably benign Het
Vmn2r58 T A 7: 41,514,703 (GRCm39) I89F probably damaging Het
Xirp2 A G 2: 67,343,849 (GRCm39) D2030G probably benign Het
Zfp326 T C 5: 106,036,451 (GRCm39) S121P probably damaging Het
Other mutations in Vmn1r177
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01456:Vmn1r177 APN 7 23,565,753 (GRCm39) missense possibly damaging 0.58
IGL01504:Vmn1r177 APN 7 23,565,835 (GRCm39) missense probably damaging 0.98
IGL01535:Vmn1r177 APN 7 23,565,765 (GRCm39) missense probably damaging 1.00
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 2013-12-09