Incidental Mutation 'IGL01875:Vmn2r35'
ID178888
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r35
Ensembl Gene ENSMUSG00000096399
Gene Namevomeronasal 2, receptor 35
SynonymsEG625353
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01875
Quality Score
Status
Chromosome7
Chromosomal Location7786151-7819867 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 7816773 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000133007 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169683]
Predicted Effect probably benign
Transcript: ENSMUST00000169683
SMART Domains Protein: ENSMUSP00000133007
Gene: ENSMUSG00000096399

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 1.8e-32 PFAM
Pfam:NCD3G 512 565 1.2e-18 PFAM
Pfam:7tm_3 595 833 2.4e-55 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
Vmn1r91 T A 7: 20,101,934 C259* probably null Het
Vmn2r16 T C 5: 109,330,411 F11L probably benign Het
Vmn2r28 T A 7: 5,481,303 M633L 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 Vmn2r35
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03334:Vmn2r35 APN 7 7786494 missense probably damaging 1.00
R1858:Vmn2r35 UTSW 7 7816806 missense possibly damaging 0.46
R5505:Vmn2r35 UTSW 7 7786480 missense probably damaging 1.00
R6150:Vmn2r35 UTSW 7 7786556 missense probably damaging 1.00
R6211:Vmn2r35 UTSW 7 7786528 missense probably damaging 0.99
R7439:Vmn2r35 UTSW 7 7817014 missense probably damaging 1.00
R8399:Vmn2r35 UTSW 7 7816898 missense probably benign 0.00
Posted On2014-05-07