Incidental Mutation 'IGL02593:Vmn2r-ps129'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r-ps129
Ensembl Gene ENSMUSG00000094752
Gene Namevomeronasal 2, receptor, pseudogene 129
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02593
Quality Score
Chromosomal Location22992706-23008970 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to T at 22992796 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000177509
SMART Domains Protein: ENSMUSP00000135413
Gene: ENSMUSG00000094752

signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 76 469 1.3e-22 PFAM
Pfam:NCD3G 511 563 1.1e-19 PFAM
Pfam:7tm_3 593 687 4.9e-19 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahsg G T 16: 22,892,328 probably null Het
Bbs4 C T 9: 59,328,597 D232N probably damaging Het
Cdh23 A T 10: 60,465,995 probably benign Het
Cntn5 T C 9: 9,833,499 N554S probably damaging Het
Fn1 T C 1: 71,602,432 I1652V probably benign Het
Gm17677 T A 9: 35,742,142 C81S possibly damaging Het
Gm364 G A X: 57,421,960 D245N probably benign Het
Golga4 T C 9: 118,555,566 probably benign Het
Idh3a T A 9: 54,596,193 probably benign Het
Jph2 T C 2: 163,397,246 Y94C probably damaging Het
Lnx2 A G 5: 147,033,015 S238P possibly damaging Het
Loxhd1 A G 18: 77,410,539 I56V possibly damaging Het
Myo9b A C 8: 71,290,773 E159D probably damaging Het
Nkiras1 A G 14: 18,278,475 N63S possibly damaging Het
Nnmt A G 9: 48,604,803 probably null Het
Olfr535 G A 7: 140,493,331 R231H probably benign Het
P2ry10 T C X: 107,102,696 I79T possibly damaging Het
Padi2 A G 4: 140,949,842 H647R probably damaging Het
Ptchd4 A G 17: 42,317,146 D166G probably benign Het
Scml2 T C X: 161,187,309 V125A probably benign Het
Senp2 A G 16: 22,044,271 D556G probably damaging Het
Serpina3a G T 12: 104,118,432 V29L probably benign Het
Sgcz A T 8: 37,523,278 I307N probably damaging Het
Slc25a13 C T 6: 6,042,265 V638I probably benign Het
Snx7 G A 3: 117,839,960 L84F probably damaging Het
Ticrr A G 7: 79,695,466 D1693G probably damaging Het
Vmn2r7 C T 3: 64,693,022 C485Y probably damaging Het
Zfyve9 A G 4: 108,682,223 V951A possibly damaging Het
Other mutations in Vmn2r-ps129
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02445:Vmn2r-ps129 APN 17 23008419 exon noncoding transcript
R6036:Vmn2r-ps129 UTSW 17 22995172 critical splice donor site noncoding transcript
Posted On2015-04-16