Incidental Mutation 'IGL01070:Vmn1r64'
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ID51447
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r64
Ensembl Gene ENSMUSG00000058399
Gene Namevomeronasal 1 receptor 64
SynonymsV1rd11
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.052) question?
Stock #IGL01070
Quality Score
Status
Chromosome7
Chromosomal Location5883580-5884590 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 5883942 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Serine at position 201 (A201S)
Ref Sequence ENSEMBL: ENSMUSP00000077568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078475]
Predicted Effect probably benign
Transcript: ENSMUST00000078475
AA Change: A201S

PolyPhen 2 Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000077568
Gene: ENSMUSG00000058399
AA Change: A201S

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 3.3e-13 PFAM
Pfam:V1R 41 296 1.5e-19 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,950,275 V124I probably damaging Het
Adamts5 T C 16: 85,863,133 H757R probably damaging Het
Aen G A 7: 78,907,302 M299I probably damaging Het
Akap3 A T 6: 126,865,879 E487V possibly damaging Het
Bicd2 T C 13: 49,378,316 S271P probably damaging Het
Cfap206 C T 4: 34,721,562 S162N probably damaging Het
Cma1 A G 14: 55,942,697 S71P probably benign Het
Cspp1 T C 1: 10,088,145 Y494H probably damaging Het
Cyp39a1 A G 17: 43,683,022 K191R probably benign Het
Efr3a G A 15: 65,853,078 V507I probably benign Het
Fam178b C T 1: 36,564,403 R489Q possibly damaging Het
Kcnj4 A G 15: 79,484,579 L400P probably benign Het
Kif27 A G 13: 58,344,093 Y411H probably damaging Het
Mstn A T 1: 53,061,997 I78L possibly damaging Het
Nrap T C 19: 56,329,084 D1377G probably damaging Het
Pramel5 T G 4: 144,271,272 Y467S probably damaging Het
Prkg1 G A 19: 30,569,343 probably benign Het
Rbfox1 A C 16: 7,306,443 S219R possibly damaging Het
Rfng T C 11: 120,783,952 N71D probably damaging Het
Rp1 T C 1: 4,345,238 I1884V probably damaging Het
Rptn T A 3: 93,398,176 Y939N possibly damaging Het
Sart1 A G 19: 5,383,951 V322A probably benign Het
Shank3 T C 15: 89,549,416 S1455P probably damaging Het
Smc5 T A 19: 23,231,601 R703W possibly damaging Het
Sptan1 G A 2: 30,014,173 probably null Het
Tecta T C 9: 42,395,003 D43G probably damaging Het
Tmem67 A T 4: 12,054,750 M685K probably benign Het
Trac A G 14: 54,220,766 T82A probably benign Het
Trank1 A G 9: 111,366,793 N1295S probably damaging Het
Ttc36 T C 9: 44,801,590 probably null Het
Utp18 A T 11: 93,869,848 S384T possibly damaging Het
Vmn2r26 A T 6: 124,061,607 I714F probably benign Het
Vps54 T A 11: 21,312,268 V626D probably damaging Het
Wapl T C 14: 34,745,622 probably benign Het
Yars2 C T 16: 16,306,542 R338* probably null Het
Other mutations in Vmn1r64
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00161:Vmn1r64 APN 7 5883828 missense probably damaging 0.98
IGL01817:Vmn1r64 APN 7 5884223 missense probably damaging 1.00
IGL02026:Vmn1r64 APN 7 5883650 missense possibly damaging 0.84
IGL02657:Vmn1r64 APN 7 5883728 missense probably benign 0.33
IGL03352:Vmn1r64 APN 7 5884071 missense probably benign 0.12
R0200:Vmn1r64 UTSW 7 5883818 missense probably benign 0.38
R0540:Vmn1r64 UTSW 7 5884097 missense probably damaging 1.00
R0655:Vmn1r64 UTSW 7 5884208 missense probably benign 0.25
R1212:Vmn1r64 UTSW 7 5884211 missense probably damaging 1.00
R1579:Vmn1r64 UTSW 7 5883804 missense probably damaging 1.00
R2034:Vmn1r64 UTSW 7 5883989 missense probably benign 0.09
R2221:Vmn1r64 UTSW 7 5884449 missense probably benign 0.00
R2240:Vmn1r64 UTSW 7 5884370 nonsense probably null
R2305:Vmn1r64 UTSW 7 5884536 missense probably benign 0.04
R3019:Vmn1r64 UTSW 7 5884227 missense probably damaging 1.00
R4256:Vmn1r64 UTSW 7 5883896 missense probably benign 0.05
R4666:Vmn1r64 UTSW 7 5884358 missense probably damaging 0.99
R4996:Vmn1r64 UTSW 7 5884053 missense probably benign 0.03
R5682:Vmn1r64 UTSW 7 5883623 missense possibly damaging 0.79
R5730:Vmn1r64 UTSW 7 5884523 missense probably benign 0.01
R7397:Vmn1r64 UTSW 7 5884014 missense possibly damaging 0.87
X0063:Vmn1r64 UTSW 7 5884350 missense probably benign 0.00
Posted On2013-06-21