Incidental Mutation 'IGL01875:Vmn1r91'
ID178847
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r91
Ensembl Gene ENSMUSG00000095201
Gene Namevomeronasal 1 receptor 91
SynonymsGm8442
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.136) question?
Stock #IGL01875
Quality Score
Status
Chromosome7
Chromosomal Location20101158-20102081 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 20101934 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Stop codon at position 259 (C259*)
Ref Sequence ENSEMBL: ENSMUSP00000129283 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165330]
Predicted Effect probably null
Transcript: ENSMUST00000165330
AA Change: C259*
SMART Domains Protein: ENSMUSP00000129283
Gene: ENSMUSG00000095201
AA Change: C259*

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 5.1e-18 PFAM
Pfam:V1R 41 298 7.1e-15 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam11 A G 11: 102,772,856 T287A probably damaging Het
Afm G T 5: 90,548,883 probably benign Het
Ankrd24 A G 10: 81,629,737 probably benign Het
Ankrd53 G T 6: 83,763,049 E62* probably null Het
Atg4b A G 1: 93,778,310 S162G probably damaging Het
B530045E10Rik A T 10: 99,422,315 noncoding transcript Het
Ccng1 A G 11: 40,752,356 V88A probably benign Het
Ces1e T A 8: 93,223,896 M86L probably benign Het
Chrne A T 11: 70,618,672 probably null Het
Ctsh T C 9: 90,064,207 S109P probably damaging Het
Eif4g1 A C 16: 20,681,040 I420L probably damaging Het
Ep300 T A 15: 81,640,023 S1351T unknown Het
Fgfr1 A G 8: 25,573,553 M732V possibly damaging Het
Gata5 T G 2: 180,327,345 probably benign Het
Gm10717 C T 9: 3,025,616 S67L probably benign Het
Gm3633 A T 14: 42,639,277 M18K probably damaging Het
Gucy1b2 A G 14: 62,420,146 L211P probably damaging Het
Hemgn T C 4: 46,396,994 N81D possibly damaging Het
Irs2 A T 8: 11,006,221 M737K probably damaging Het
Itgb7 C A 15: 102,217,995 C502F probably damaging Het
Jakmip1 G T 5: 37,120,980 A534S probably damaging Het
Kidins220 A G 12: 25,057,729 H1636R probably benign Het
Kirrel T A 3: 87,095,730 I119F probably damaging Het
Lrba T C 3: 86,310,047 V527A probably damaging Het
Mitf A G 6: 98,017,895 E409G probably benign Het
Mtrr T G 13: 68,572,609 K289T probably damaging Het
Muc2 A T 7: 141,752,740 I739F probably damaging Het
Ncor2 T C 5: 125,065,870 T612A unknown Het
Olfr1126 T A 2: 87,457,310 N48K probably damaging Het
Olfr54 A T 11: 51,027,375 R124S probably damaging Het
Olfr806 T A 10: 129,738,922 probably benign Het
Olfr901 T A 9: 38,430,298 N5K probably damaging Het
P4ha3 T A 7: 100,300,652 C109S probably damaging Het
Prkd3 T C 17: 78,957,206 E660G possibly damaging Het
Rbm4b G A 19: 4,762,191 M209I probably benign Het
Reln T A 5: 21,904,717 T3132S probably benign Het
Selenbp2 T A 3: 94,698,144 D92E possibly damaging Het
Slfn8 G T 11: 83,004,079 Q634K probably benign Het
Sumo3 A T 10: 77,613,998 I57F probably benign Het
Tacr1 A G 6: 82,557,016 Y341C probably benign Het
Tlr4 T A 4: 66,839,489 L173Q probably damaging Het
Tshz3 C T 7: 36,769,960 T458M probably damaging Het
Vmn2r16 T C 5: 109,330,411 F11L probably benign Het
Vmn2r28 T A 7: 5,481,303 M633L probably benign Het
Vmn2r35 T C 7: 7,816,773 probably benign Het
Vwc2l G T 1: 70,729,013 A79S probably benign Het
Zfhx2 G A 14: 55,063,915 S2204F unknown Het
Other mutations in Vmn1r91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02125:Vmn1r91 APN 7 20101504 missense probably damaging 0.96
IGL02263:Vmn1r91 APN 7 20101843 missense probably benign 0.00
IGL02338:Vmn1r91 APN 7 20101746 missense probably damaging 0.96
IGL02708:Vmn1r91 APN 7 20101490 missense probably damaging 1.00
R1880:Vmn1r91 UTSW 7 20101773 missense probably damaging 1.00
R2679:Vmn1r91 UTSW 7 20102058 missense probably damaging 0.97
R4730:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R5362:Vmn1r91 UTSW 7 20101461 missense probably benign 0.05
R5633:Vmn1r91 UTSW 7 20101945 missense possibly damaging 0.56
R5979:Vmn1r91 UTSW 7 20102065 missense probably benign 0.00
R6151:Vmn1r91 UTSW 7 20101435 missense probably benign
R6177:Vmn1r91 UTSW 7 20101479 missense possibly damaging 0.95
R7397:Vmn1r91 UTSW 7 20101770 missense possibly damaging 0.71
R7589:Vmn1r91 UTSW 7 20101877 missense probably benign 0.07
R7872:Vmn1r91 UTSW 7 20101914 missense probably benign 0.26
R7886:Vmn1r91 UTSW 7 20101565 missense probably benign
R7903:Vmn1r91 UTSW 7 20101210 missense possibly damaging 0.88
R7953:Vmn1r91 UTSW 7 20101293 missense possibly damaging 0.68
R8043:Vmn1r91 UTSW 7 20101293 missense possibly damaging 0.68
R8202:Vmn1r91 UTSW 7 20101824 missense probably damaging 1.00
Posted On2014-05-07