Incidental Mutation 'IGL02794:Vmn1r211'
ID 359869
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r211
Ensembl Gene ENSMUSG00000063998
Gene Name vomeronasal 1 receptor 211
Synonyms V1rh20
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL02794
Quality Score
Status
Chromosome 13
Chromosomal Location 23035769-23036665 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 23036379 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Asparagine at position 96 (T96N)
Ref Sequence ENSEMBL: ENSMUSP00000154146 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073728] [ENSMUST00000228645]
AlphaFold Q8R266
Predicted Effect possibly damaging
Transcript: ENSMUST00000073728
AA Change: T96N

PolyPhen 2 Score 0.907 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000073405
Gene: ENSMUSG00000063998
AA Change: T96N

DomainStartEndE-ValueType
Pfam:V1R 31 297 1.1e-40 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000228645
AA Change: T96N

PolyPhen 2 Score 0.907 (Sensitivity: 0.81; Specificity: 0.94)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 T A 17: 24,621,385 (GRCm39) C1082S probably benign Het
Akt2 G T 7: 27,328,806 (GRCm39) R176L probably benign Het
Aldh16a1 A G 7: 44,795,018 (GRCm39) Y484H probably damaging Het
Apeh A G 9: 107,969,209 (GRCm39) S280P possibly damaging Het
Atp1a4 T C 1: 172,071,653 (GRCm39) M481V probably benign Het
Atraid G A 5: 31,210,214 (GRCm39) S135N probably damaging Het
Camta2 C T 11: 70,566,484 (GRCm39) G677D possibly damaging Het
Ccdc18 A G 5: 108,319,614 (GRCm39) N545S probably benign Het
Cic A G 7: 24,985,069 (GRCm39) D1105G probably damaging Het
Crisp1 A T 17: 40,623,957 (GRCm39) M4K unknown Het
Crnkl1 C T 2: 145,772,532 (GRCm39) E182K possibly damaging Het
Dnmt1 A T 9: 20,847,847 (GRCm39) C114S probably benign Het
Dsc2 A T 18: 20,174,788 (GRCm39) Y496N probably damaging Het
Dst T C 1: 34,309,910 (GRCm39) V1528A probably damaging Het
Fbxl8 C T 8: 105,994,752 (GRCm39) T88M probably benign Het
Fbxo10 T C 4: 45,041,928 (GRCm39) N767S probably benign Het
Gm1527 A G 3: 28,949,829 (GRCm39) T30A unknown Het
Gorasp2 C A 2: 70,509,838 (GRCm39) Y166* probably null Het
Gucy2c T A 6: 136,690,146 (GRCm39) Q744L probably damaging Het
Heg1 A T 16: 33,546,992 (GRCm39) N593I probably damaging Het
Ice1 T A 13: 70,757,278 (GRCm39) S236C possibly damaging Het
Il12b T C 11: 44,298,808 (GRCm39) Y88H probably damaging Het
Izumo3 C T 4: 92,035,200 (GRCm39) V6I probably benign Het
Kcna6 A G 6: 126,715,515 (GRCm39) V458A probably damaging Het
Kif13b G A 14: 65,040,889 (GRCm39) R1659Q probably benign Het
Klk1b1 A G 7: 43,619,789 (GRCm39) D116G possibly damaging Het
Lama2 T C 10: 26,917,227 (GRCm39) T2233A possibly damaging Het
Lin9 A T 1: 180,479,444 (GRCm39) K59N probably damaging Het
Ltbp2 T C 12: 84,838,709 (GRCm39) E1083G probably damaging Het
Mfsd11 T A 11: 116,750,177 (GRCm39) S105T probably damaging Het
Mga T A 2: 119,776,770 (GRCm39) I1768N possibly damaging Het
Mical3 C A 6: 120,984,270 (GRCm39) G202V probably damaging Het
Mylk A T 16: 34,806,911 (GRCm39) I1719F probably benign Het
Nusap1 T A 2: 119,460,867 (GRCm39) F120Y possibly damaging Het
Or52e8 T A 7: 104,624,596 (GRCm39) M203L probably benign Het
Or8b56 T A 9: 38,739,511 (GRCm39) C175S probably damaging Het
Or8k32 T C 2: 86,368,492 (GRCm39) T256A possibly damaging Het
Pidd1 T C 7: 141,023,021 (GRCm39) Y57C probably benign Het
Pik3cd T A 4: 149,739,028 (GRCm39) M671L probably benign Het
Ppp5c A G 7: 16,740,885 (GRCm39) V361A probably benign Het
Prune2 T C 19: 17,096,725 (GRCm39) V743A probably benign Het
Siglec1 C A 2: 130,917,889 (GRCm39) S996I possibly damaging Het
Slc12a7 A G 13: 73,957,206 (GRCm39) R948G possibly damaging Het
Slc40a1 A T 1: 45,948,668 (GRCm39) Y537* probably null Het
Smarca4 T A 9: 21,584,638 (GRCm39) probably benign Het
Smg6 C T 11: 74,944,760 (GRCm39) P1109S probably damaging Het
Sorl1 T A 9: 41,975,070 (GRCm39) N513Y probably damaging Het
Trim58 C T 11: 58,531,292 (GRCm39) probably benign Het
Trim72 T C 7: 127,603,704 (GRCm39) C17R probably damaging Het
Ttc3 T C 16: 94,268,785 (GRCm39) C1956R probably damaging Het
Vmn2r66 A T 7: 84,644,623 (GRCm39) S596T probably benign Het
Zfp609 A G 9: 65,611,602 (GRCm39) S454P possibly damaging Het
Other mutations in Vmn1r211
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Vmn1r211 APN 13 23,036,272 (GRCm39) missense probably benign 0.00
IGL01583:Vmn1r211 APN 13 23,036,571 (GRCm39) missense probably benign 0.40
IGL02735:Vmn1r211 APN 13 23,036,418 (GRCm39) missense probably damaging 1.00
IGL02794:Vmn1r211 APN 13 23,036,377 (GRCm39) missense probably damaging 1.00
IGL02794:Vmn1r211 APN 13 23,036,376 (GRCm39) missense probably damaging 0.99
IGL03292:Vmn1r211 APN 13 23,036,613 (GRCm39) missense probably damaging 1.00
R1456:Vmn1r211 UTSW 13 23,036,415 (GRCm39) missense probably damaging 1.00
R1682:Vmn1r211 UTSW 13 23,035,813 (GRCm39) missense probably damaging 0.97
R1868:Vmn1r211 UTSW 13 23,035,779 (GRCm39) missense probably benign 0.07
R2002:Vmn1r211 UTSW 13 23,035,953 (GRCm39) missense probably damaging 1.00
R2037:Vmn1r211 UTSW 13 23,036,134 (GRCm39) missense probably damaging 0.98
R2655:Vmn1r211 UTSW 13 23,036,586 (GRCm39) missense probably benign 0.42
R4837:Vmn1r211 UTSW 13 23,036,296 (GRCm39) missense probably benign 0.41
R6284:Vmn1r211 UTSW 13 23,036,254 (GRCm39) missense probably damaging 0.99
R6701:Vmn1r211 UTSW 13 23,035,779 (GRCm39) missense probably benign 0.07
R6715:Vmn1r211 UTSW 13 23,035,949 (GRCm39) missense probably benign 0.00
R7058:Vmn1r211 UTSW 13 23,036,063 (GRCm39) missense probably benign 0.15
R7465:Vmn1r211 UTSW 13 23,036,086 (GRCm39) missense probably benign 0.13
R8085:Vmn1r211 UTSW 13 23,035,953 (GRCm39) missense probably damaging 1.00
R8720:Vmn1r211 UTSW 13 23,036,031 (GRCm39) missense probably damaging 1.00
R8730:Vmn1r211 UTSW 13 23,035,838 (GRCm39) nonsense probably null
R9120:Vmn1r211 UTSW 13 23,035,936 (GRCm39) missense probably damaging 1.00
R9725:Vmn1r211 UTSW 13 23,036,506 (GRCm39) missense probably benign 0.03
Posted On 2015-12-18