Incidental Mutation 'IGL01955:Vmn1r82'
ID181433
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r82
Ensembl Gene ENSMUSG00000058132
Gene Namevomeronasal 1 receptor 82
SynonymsV1rg12
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock #IGL01955
Quality Score
Status
Chromosome7
Chromosomal Location12300430-12308582 bp(+) (GRCm38)
Type of Mutationunclassified (4 bp from exon)
DNA Base Change (assembly) A to C at 12305723 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140782 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072801] [ENSMUST00000191002] [ENSMUST00000227672]
Predicted Effect probably benign
Transcript: ENSMUST00000072801
SMART Domains Protein: ENSMUSP00000072580
Gene: ENSMUSG00000058132

DomainStartEndE-ValueType
Pfam:V1R 35 295 1.3e-28 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000191002
SMART Domains Protein: ENSMUSP00000140782
Gene: ENSMUSG00000058132

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:V1R 36 296 8.4e-27 PFAM
Pfam:7tm_1 39 290 2e-5 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227672
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930432E11Rik G T 7: 29,573,995 noncoding transcript Het
Abcc1 T A 16: 14,410,795 I302N probably damaging Het
Abhd16a A G 17: 35,101,340 S394G probably damaging Het
Adgrv1 T C 13: 81,182,783 Y71C probably damaging Het
Apol8 A G 15: 77,749,699 C226R probably benign Het
Armc4 C T 18: 7,127,291 R974Q possibly damaging Het
Bbs7 A G 3: 36,610,322 S45P probably benign Het
Cacna1b T C 2: 24,639,137 Y1575C probably damaging Het
Cckbr T A 7: 105,434,962 V301E probably damaging Het
Cwc27 A G 13: 104,807,737 Y79H probably damaging Het
Dchs1 T C 7: 105,757,591 T2236A probably benign Het
Ddx50 T C 10: 62,647,183 R36G probably benign Het
Extl3 T A 14: 65,075,966 Y589F probably benign Het
Gab2 T C 7: 97,304,223 V601A probably damaging Het
Hsd3b1 T A 3: 98,853,147 N176I probably benign Het
L3mbtl3 A T 10: 26,318,438 S420R unknown Het
Olfr1000 A G 2: 85,608,707 F68L probably benign Het
Olfr319 T C 11: 58,702,129 S143P probably damaging Het
Olfr589 T A 7: 103,154,854 K298* probably null Het
Polr2a T C 11: 69,741,848 D974G probably damaging Het
Ptges3l T C 11: 101,423,818 K13E possibly damaging Het
Ptprk A G 10: 28,595,865 probably benign Het
Rassf3 T C 10: 121,417,122 Y60C probably damaging Het
Rnf157 T C 11: 116,359,896 T160A probably damaging Het
Secisbp2l A G 2: 125,743,812 probably null Het
Setd2 A G 9: 110,549,318 T734A probably benign Het
Skint5 A G 4: 113,623,736 probably null Het
Slc38a9 A G 13: 112,695,418 probably benign Het
Snx17 T G 5: 31,197,082 probably benign Het
Tas2r113 A T 6: 132,893,854 M282L probably benign Het
Tbc1d31 A G 15: 57,942,370 N404D probably benign Het
Tmem63c A T 12: 87,077,208 I487F probably benign Het
Tpm3 A G 3: 90,088,435 M164V probably benign Het
Trafd1 G T 5: 121,375,154 N340K probably benign Het
Trpv4 T A 5: 114,622,682 K863* probably null Het
Ttn A T 2: 76,797,352 M13003K possibly damaging Het
Tulp1 G A 17: 28,356,424 T103M probably damaging Het
Unc5b T C 10: 60,778,255 T272A probably benign Het
Zc3h7b A G 15: 81,792,004 N704D probably benign Het
Other mutations in Vmn1r82
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01509:Vmn1r82 APN 7 12305169 missense probably damaging 0.99
IGL02267:Vmn1r82 APN 7 12305346 missense probably damaging 1.00
R0336:Vmn1r82 UTSW 7 12305321 missense probably benign 0.26
R2373:Vmn1r82 UTSW 7 12305055 missense probably damaging 0.99
R2849:Vmn1r82 UTSW 7 12305406 missense probably damaging 1.00
R4621:Vmn1r82 UTSW 7 12305336 missense possibly damaging 0.71
R5628:Vmn1r82 UTSW 7 12305278 missense probably damaging 1.00
R6180:Vmn1r82 UTSW 7 12305085 missense probably damaging 0.97
R6263:Vmn1r82 UTSW 7 12305534 missense probably damaging 1.00
R6877:Vmn1r82 UTSW 7 12305363 missense possibly damaging 0.79
Posted On2014-05-07