Incidental Mutation 'IGL02936:Vmn1r15'
ID364299
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r15
Ensembl Gene ENSMUSG00000115199
Gene Namevomeronasal 1 receptor 15
SynonymsV1rc6
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.112) question?
Stock #IGL02936
Quality Score
Status
Chromosome6
Chromosomal Location57257952-57259972 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 57258818 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Stop codon at position 224 (K224*)
Ref Sequence ENSEMBL: ENSMUSP00000154252 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071304] [ENSMUST00000228297]
Predicted Effect probably null
Transcript: ENSMUST00000071304
AA Change: K224*
SMART Domains Protein: ENSMUSP00000071272
Gene: ENSMUSG00000115236
AA Change: K224*

DomainStartEndE-ValueType
Pfam:V1R 28 293 4.5e-56 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000228297
AA Change: K224*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik G A 9: 57,258,404 T229I possibly damaging Het
Acad11 T C 9: 104,113,512 S439P probably benign Het
Acer2 A T 4: 86,900,559 N148I possibly damaging Het
Adgre1 A G 17: 57,478,833 I860V probably benign Het
Asb2 A G 12: 103,335,914 I125T probably benign Het
Atp13a2 G T 4: 141,001,949 L614F probably benign Het
Car7 A G 8: 104,548,222 T132A possibly damaging Het
Ccdc36 T C 9: 108,412,503 I173M possibly damaging Het
Cfap221 T C 1: 119,984,752 D135G probably damaging Het
Crtc3 A G 7: 80,589,763 F614L probably damaging Het
Csn3 T G 5: 87,930,133 I166S possibly damaging Het
Dna2 T G 10: 62,957,100 L298R probably damaging Het
Ece1 T C 4: 137,946,301 S387P probably benign Het
Fbxo28 C T 1: 182,341,528 G15D unknown Het
Fbxw24 A T 9: 109,624,958 probably null Het
Foxd3 T A 4: 99,656,815 V64E probably benign Het
Galnt7 A C 8: 57,584,214 V47G probably benign Het
Gcc2 A T 10: 58,296,140 L1453F probably damaging Het
Gcnt4 G A 13: 96,946,411 V72I probably benign Het
Gm10269 A C 18: 20,682,953 probably null Het
Hmcn1 T G 1: 150,697,522 Q2125H probably damaging Het
Llcfc1 T A 6: 41,684,659 S48T probably benign Het
Met G T 6: 17,553,397 V1061F probably damaging Het
Mthfd2 G A 6: 83,311,360 H138Y probably damaging Het
Mtus1 A T 8: 40,999,517 D1041E possibly damaging Het
Mug2 G A 6: 122,081,387 probably null Het
Nos3 C T 5: 24,380,993 T878I probably damaging Het
Olfr1211 A G 2: 88,929,784 M177T probably benign Het
Olfr690 A T 7: 105,330,005 Y62* probably null Het
Pbrm1 T A 14: 31,061,513 V497D probably damaging Het
Plcd1 T C 9: 119,074,199 E471G probably damaging Het
Poc1a A G 9: 106,285,027 T84A probably damaging Het
Ppm1f A G 16: 16,915,236 H209R probably damaging Het
Rccd1 T A 7: 80,317,046 K329N probably damaging Het
Serpinb9g A T 13: 33,494,882 N245I possibly damaging Het
Slc22a26 A C 19: 7,791,105 F196V probably damaging Het
Tial1 G A 7: 128,442,663 probably benign Het
Trpa1 A T 1: 14,875,969 probably null Het
Wdr72 A T 9: 74,152,580 D424V probably damaging Het
Wt1 A G 2: 105,169,039 K308E probably damaging Het
Zwint T C 10: 72,657,124 S193P probably damaging Het
Other mutations in Vmn1r15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01645:Vmn1r15 APN 6 57258562 nonsense probably null
IGL02326:Vmn1r15 APN 6 57258270 missense probably benign 0.02
IGL02431:Vmn1r15 APN 6 57258903 missense possibly damaging 0.94
IGL02990:Vmn1r15 APN 6 57258608 missense probably benign 0.14
IGL03177:Vmn1r15 APN 6 57258473 missense probably benign 0.27
IGL03382:Vmn1r15 APN 6 57258570 missense probably benign 0.04
R0531:Vmn1r15 UTSW 6 57258251 missense probably benign 0.10
R1858:Vmn1r15 UTSW 6 57258631 missense probably benign 0.13
R2010:Vmn1r15 UTSW 6 57258284 missense probably benign 0.02
R2055:Vmn1r15 UTSW 6 57258744 missense possibly damaging 0.90
R2291:Vmn1r15 UTSW 6 57258692 missense possibly damaging 0.93
R3697:Vmn1r15 UTSW 6 57258336 missense possibly damaging 0.63
R5161:Vmn1r15 UTSW 6 57258512 missense probably benign 0.00
R5884:Vmn1r15 UTSW 6 57259008 missense probably damaging 0.99
R7287:Vmn1r15 UTSW 6 57258216 missense possibly damaging 0.63
R7376:Vmn1r15 UTSW 6 57258357 missense probably benign 0.11
R7773:Vmn1r15 UTSW 6 57258659 missense probably benign 0.05
R7980:Vmn1r15 UTSW 6 57258414 missense probably damaging 1.00
R8309:Vmn1r15 UTSW 6 57258650 missense probably benign 0.01
Posted On2015-12-18