Incidental Mutation 'IGL03077:Vmn1r191'
ID 417709
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r191
Ensembl Gene ENSMUSG00000095916
Gene Name vomeronasal 1 receptor 191
Synonyms V1rh15
Accession Numbers
Essential gene? Probably non essential (E-score: 0.153) question?
Stock # IGL03077
Quality Score
Status
Chromosome 13
Chromosomal Location 22362856-22363752 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 22363316 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Serine at position 146 (I146S)
Ref Sequence ENSEMBL: ENSMUSP00000072206 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072369]
AlphaFold Q8K4D0
Predicted Effect probably benign
Transcript: ENSMUST00000072369
AA Change: I146S

PolyPhen 2 Score 0.073 (Sensitivity: 0.93; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000072206
Gene: ENSMUSG00000095916
AA Change: I146S

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
Pfam:V1R 35 291 4.4e-33 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120067
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg8 A G 17: 84,999,308 (GRCm39) N135D probably damaging Het
Ak4 T C 4: 101,277,148 (GRCm39) L44P probably damaging Het
Angpt1 C A 15: 42,339,818 (GRCm39) G298* probably null Het
Appl2 C T 10: 83,457,623 (GRCm39) probably benign Het
Arhgap19 T A 19: 41,769,760 (GRCm39) H341L probably benign Het
Chmp5 T C 4: 40,952,438 (GRCm39) S98P probably benign Het
Chp1 A T 2: 119,415,081 (GRCm39) Q161L probably benign Het
Clgn T C 8: 84,150,769 (GRCm39) V478A probably benign Het
Cplane1 G A 15: 8,242,279 (GRCm39) probably benign Het
Cyp2b19 A T 7: 26,461,809 (GRCm39) M210L probably benign Het
Eif4g3 T A 4: 137,853,166 (GRCm39) V244D probably damaging Het
Ftcd T C 10: 76,417,461 (GRCm39) I300T probably damaging Het
Gm12886 C T 4: 121,272,697 (GRCm39) probably benign Het
Klrb1f A T 6: 129,030,765 (GRCm39) E92V probably null Het
Krt23 A G 11: 99,374,700 (GRCm39) probably benign Het
Mib2 T G 4: 155,743,900 (GRCm39) R47S probably benign Het
Mindy4 A G 6: 55,286,315 (GRCm39) T728A probably damaging Het
Myh15 A G 16: 48,916,901 (GRCm39) N407S probably benign Het
Nlrp4f A G 13: 65,342,412 (GRCm39) V411A probably benign Het
Or10ag56 T C 2: 87,140,056 (GRCm39) *328Q probably null Het
Or4c12b A C 2: 89,647,486 (GRCm39) D266A probably damaging Het
Otud4 T G 8: 80,400,087 (GRCm39) S934A probably damaging Het
P3h1 C T 4: 119,093,983 (GRCm39) R213W probably damaging Het
Phrf1 A T 7: 140,834,881 (GRCm39) K19* probably null Het
Prl3b1 A T 13: 27,429,759 (GRCm39) M66L probably benign Het
Psmd7 T C 8: 108,309,099 (GRCm39) T149A probably benign Het
Samd4b T C 7: 28,105,868 (GRCm39) D450G probably damaging Het
Scn3a G A 2: 65,367,016 (GRCm39) A2V probably damaging Het
Snrpa G A 7: 26,891,186 (GRCm39) T95I probably benign Het
Traip A G 9: 107,840,125 (GRCm39) probably benign Het
Trbc1 T A 6: 41,515,383 (GRCm39) probably benign Het
Trim72 A T 7: 127,607,013 (GRCm39) M181L probably benign Het
Ttc41 T C 10: 86,594,212 (GRCm39) Y882H probably damaging Het
Vmn2r9 G T 5: 108,996,173 (GRCm39) probably benign Het
Vps13a A G 19: 16,688,246 (GRCm39) S854P probably benign Het
Wdfy1 T C 1: 79,692,622 (GRCm39) K232E possibly damaging Het
Xpr1 A T 1: 155,156,774 (GRCm39) D625E possibly damaging Het
Zbbx T A 3: 74,989,153 (GRCm39) T317S possibly damaging Het
Other mutations in Vmn1r191
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00233:Vmn1r191 APN 13 22,362,890 (GRCm39) missense probably damaging 1.00
IGL01645:Vmn1r191 APN 13 22,363,614 (GRCm39) missense probably benign 0.03
IGL02224:Vmn1r191 APN 13 22,363,068 (GRCm39) missense probably damaging 1.00
IGL02321:Vmn1r191 APN 13 22,363,068 (GRCm39) nonsense probably null
IGL02516:Vmn1r191 APN 13 22,363,710 (GRCm39) missense probably benign 0.38
IGL02602:Vmn1r191 APN 13 22,363,635 (GRCm39) missense probably damaging 1.00
IGL02630:Vmn1r191 APN 13 22,363,431 (GRCm39) missense possibly damaging 0.95
IGL03380:Vmn1r191 APN 13 22,363,055 (GRCm39) missense probably damaging 0.99
R0571:Vmn1r191 UTSW 13 22,363,217 (GRCm39) missense probably damaging 0.96
R0981:Vmn1r191 UTSW 13 22,363,389 (GRCm39) missense probably benign 0.00
R1672:Vmn1r191 UTSW 13 22,363,262 (GRCm39) missense probably benign 0.01
R1955:Vmn1r191 UTSW 13 22,362,985 (GRCm39) missense possibly damaging 0.79
R1969:Vmn1r191 UTSW 13 22,362,952 (GRCm39) missense possibly damaging 0.71
R5059:Vmn1r191 UTSW 13 22,363,163 (GRCm39) missense probably damaging 1.00
R6484:Vmn1r191 UTSW 13 22,362,918 (GRCm39) missense probably benign 0.00
R6736:Vmn1r191 UTSW 13 22,363,720 (GRCm39) missense probably benign 0.14
R7063:Vmn1r191 UTSW 13 22,362,864 (GRCm39) missense probably benign 0.08
R7475:Vmn1r191 UTSW 13 22,362,942 (GRCm39) missense probably benign 0.00
R9699:Vmn1r191 UTSW 13 22,363,355 (GRCm39) missense probably benign 0.25
Posted On 2016-08-02