Incidental Mutation 'IGL02797:Vmn2r70'
ID 359973
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r70
Ensembl Gene ENSMUSG00000090806
Gene Name vomeronasal 2, receptor 70
Synonyms EG620835
Accession Numbers
Essential gene? Probably non essential (E-score: 0.130) question?
Stock # IGL02797
Quality Score
Status
Chromosome 7
Chromosomal Location 85207911-85218296 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 85208295 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 727 (M727I)
Ref Sequence ENSEMBL: ENSMUSP00000129703 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168230]
AlphaFold K7N702
Predicted Effect probably benign
Transcript: ENSMUST00000168230
AA Change: M727I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000129703
Gene: ENSMUSG00000090806
AA Change: M727I

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:ANF_receptor 77 468 2.5e-28 PFAM
Pfam:NCD3G 510 562 1.5e-19 PFAM
Pfam:7tm_3 592 830 1.2e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc5 A G 16: 20,187,214 (GRCm39) M924T probably benign Het
Afg2a A G 3: 37,512,465 (GRCm39) probably benign Het
B3gat2 A G 1: 23,854,360 (GRCm39) Y218C probably damaging Het
Bcs1l T C 1: 74,629,620 (GRCm39) probably null Het
Cd109 T A 9: 78,568,995 (GRCm39) I358N probably damaging Het
Cd276 T C 9: 58,444,719 (GRCm39) D84G possibly damaging Het
Chsy1 T C 7: 65,821,412 (GRCm39) F549S probably damaging Het
Clca3a2 T C 3: 144,787,024 (GRCm39) N549S probably benign Het
Cma1 A G 14: 56,181,271 (GRCm39) S32P possibly damaging Het
Col23a1 G A 11: 51,452,743 (GRCm39) probably null Het
Ctps1 A T 4: 120,420,021 (GRCm39) I131K probably benign Het
Cyp2w1 T C 5: 139,342,628 (GRCm39) L441P probably damaging Het
Dnajc21 A G 15: 10,461,441 (GRCm39) Y170H probably damaging Het
Eif3a A T 19: 60,761,164 (GRCm39) L648Q probably damaging Het
Eif3l T A 15: 78,959,477 (GRCm39) D6E probably benign Het
Fam228a A T 12: 4,781,484 (GRCm39) L125Q probably damaging Het
Foxa2 A G 2: 147,886,045 (GRCm39) C263R possibly damaging Het
Gm17455 A G 10: 60,239,107 (GRCm39) E124G possibly damaging Het
Gpc6 T G 14: 117,163,394 (GRCm39) L16R probably damaging Het
Hdac9 A G 12: 34,443,273 (GRCm39) probably benign Het
Herc3 A G 6: 58,845,679 (GRCm39) N400S probably benign Het
Herc4 G A 10: 63,152,586 (GRCm39) probably null Het
Il12b A G 11: 44,301,180 (GRCm39) probably null Het
Lama4 A G 10: 38,932,920 (GRCm39) R599G probably null Het
Lrp1b T A 2: 41,561,069 (GRCm39) E286V Het
Mink1 C T 11: 70,501,176 (GRCm39) P784S probably damaging Het
Musk T C 4: 58,366,921 (GRCm39) F513S probably benign Het
Nfasc T A 1: 132,538,186 (GRCm39) D474V probably damaging Het
Nhsl3 C T 4: 129,117,104 (GRCm39) R565H probably damaging Het
Nos2 T G 11: 78,831,170 (GRCm39) F420V probably damaging Het
Or52ab2 A T 7: 102,970,058 (GRCm39) I147L probably benign Het
Pcdhb14 A G 18: 37,582,904 (GRCm39) Y670C probably damaging Het
Polr1b A G 2: 128,944,899 (GRCm39) E65G probably damaging Het
Ppp1r10 T G 17: 36,238,904 (GRCm39) probably null Het
Prag1 C T 8: 36,606,655 (GRCm39) R799C probably damaging Het
Prb1c T A 6: 132,340,008 (GRCm39) probably null Het
Ptch1 T C 13: 63,681,421 (GRCm39) N485S probably benign Het
Rgsl1 T C 1: 153,683,454 (GRCm39) T19A probably damaging Het
Sgpl1 A C 10: 60,937,507 (GRCm39) S507A probably benign Het
Sgpp2 A G 1: 78,393,819 (GRCm39) D274G probably benign Het
Skap1 A G 11: 96,603,843 (GRCm39) D211G possibly damaging Het
Smc3 A G 19: 53,627,189 (GRCm39) T830A probably benign Het
Smpd2 G A 10: 41,364,074 (GRCm39) T215I possibly damaging Het
Sntg2 T G 12: 30,276,891 (GRCm39) Y387S possibly damaging Het
Sorl1 T G 9: 41,948,355 (GRCm39) D810A probably damaging Het
Spop T A 11: 95,372,909 (GRCm39) I217N probably damaging Het
Stac2 T C 11: 97,934,345 (GRCm39) R120G possibly damaging Het
Stau1 A T 2: 166,791,266 (GRCm39) *496R probably null Het
Tmeff2 C T 1: 50,967,206 (GRCm39) R34C probably damaging Het
Treml2 C T 17: 48,609,739 (GRCm39) A57V possibly damaging Het
Vmn2r15 T C 5: 109,445,250 (GRCm39) D58G probably benign Het
Vmn2r7 T C 3: 64,598,666 (GRCm39) I721M possibly damaging Het
Vwa8 T A 14: 79,162,702 (GRCm39) C161S probably benign Het
Other mutations in Vmn2r70
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00978:Vmn2r70 APN 7 85,213,007 (GRCm39) missense probably benign 0.00
IGL01140:Vmn2r70 APN 7 85,214,379 (GRCm39) nonsense probably null
IGL01287:Vmn2r70 APN 7 85,218,227 (GRCm39) nonsense probably null
IGL01581:Vmn2r70 APN 7 85,213,122 (GRCm39) splice site probably null
IGL01632:Vmn2r70 APN 7 85,215,280 (GRCm39) missense probably benign 0.00
IGL01725:Vmn2r70 APN 7 85,208,594 (GRCm39) missense probably damaging 1.00
IGL02244:Vmn2r70 APN 7 85,214,211 (GRCm39) missense probably benign
IGL02288:Vmn2r70 APN 7 85,214,342 (GRCm39) missense probably benign 0.31
IGL02313:Vmn2r70 APN 7 85,214,376 (GRCm39) missense probably damaging 0.99
IGL02591:Vmn2r70 APN 7 85,214,153 (GRCm39) missense probably damaging 0.96
IGL02725:Vmn2r70 APN 7 85,214,553 (GRCm39) missense possibly damaging 0.46
R0045:Vmn2r70 UTSW 7 85,215,252 (GRCm39) missense probably damaging 1.00
R0729:Vmn2r70 UTSW 7 85,215,112 (GRCm39) missense probably benign 0.00
R0967:Vmn2r70 UTSW 7 85,208,827 (GRCm39) missense probably damaging 0.99
R1217:Vmn2r70 UTSW 7 85,208,269 (GRCm39) missense probably damaging 1.00
R1351:Vmn2r70 UTSW 7 85,214,262 (GRCm39) missense probably damaging 1.00
R1387:Vmn2r70 UTSW 7 85,207,969 (GRCm39) missense probably benign 0.12
R1483:Vmn2r70 UTSW 7 85,208,375 (GRCm39) missense probably benign 0.04
R1796:Vmn2r70 UTSW 7 85,213,011 (GRCm39) nonsense probably null
R1809:Vmn2r70 UTSW 7 85,215,130 (GRCm39) missense probably benign 0.23
R2154:Vmn2r70 UTSW 7 85,212,923 (GRCm39) missense possibly damaging 0.67
R2173:Vmn2r70 UTSW 7 85,214,290 (GRCm39) missense probably benign
R2334:Vmn2r70 UTSW 7 85,208,800 (GRCm39) missense probably benign 0.05
R2871:Vmn2r70 UTSW 7 85,208,227 (GRCm39) missense probably damaging 1.00
R2871:Vmn2r70 UTSW 7 85,208,227 (GRCm39) missense probably damaging 1.00
R3975:Vmn2r70 UTSW 7 85,208,540 (GRCm39) missense probably benign 0.00
R4525:Vmn2r70 UTSW 7 85,208,787 (GRCm39) missense probably damaging 1.00
R4527:Vmn2r70 UTSW 7 85,208,787 (GRCm39) missense probably damaging 1.00
R4535:Vmn2r70 UTSW 7 85,214,541 (GRCm39) missense probably damaging 1.00
R5181:Vmn2r70 UTSW 7 85,208,387 (GRCm39) missense probably damaging 0.99
R5600:Vmn2r70 UTSW 7 85,212,935 (GRCm39) missense probably benign 0.07
R5641:Vmn2r70 UTSW 7 85,208,572 (GRCm39) missense probably damaging 0.99
R5726:Vmn2r70 UTSW 7 85,208,315 (GRCm39) missense probably damaging 1.00
R5943:Vmn2r70 UTSW 7 85,215,199 (GRCm39) missense probably benign 0.09
R6166:Vmn2r70 UTSW 7 85,215,189 (GRCm39) missense probably benign 0.25
R6272:Vmn2r70 UTSW 7 85,208,194 (GRCm39) missense probably damaging 1.00
R6324:Vmn2r70 UTSW 7 85,208,087 (GRCm39) missense probably benign 0.01
R6429:Vmn2r70 UTSW 7 85,208,276 (GRCm39) missense probably damaging 1.00
R6449:Vmn2r70 UTSW 7 85,214,157 (GRCm39) missense probably damaging 1.00
R6512:Vmn2r70 UTSW 7 85,215,305 (GRCm39) missense probably benign
R7000:Vmn2r70 UTSW 7 85,208,819 (GRCm39) missense probably damaging 0.99
R7141:Vmn2r70 UTSW 7 85,208,044 (GRCm39) missense probably benign
R7153:Vmn2r70 UTSW 7 85,214,262 (GRCm39) missense probably damaging 1.00
R7424:Vmn2r70 UTSW 7 85,213,076 (GRCm39) missense probably damaging 1.00
R7565:Vmn2r70 UTSW 7 85,214,499 (GRCm39) missense probably benign 0.35
R7567:Vmn2r70 UTSW 7 85,214,243 (GRCm39) missense probably benign 0.41
R7593:Vmn2r70 UTSW 7 85,215,312 (GRCm39) nonsense probably null
R7660:Vmn2r70 UTSW 7 85,218,130 (GRCm39) missense probably damaging 0.99
R7806:Vmn2r70 UTSW 7 85,208,401 (GRCm39) missense probably benign
R7892:Vmn2r70 UTSW 7 85,208,588 (GRCm39) missense possibly damaging 0.58
R7965:Vmn2r70 UTSW 7 85,211,071 (GRCm39) missense probably damaging 0.96
R8052:Vmn2r70 UTSW 7 85,212,923 (GRCm39) missense probably benign
R8251:Vmn2r70 UTSW 7 85,215,186 (GRCm39) nonsense probably null
R8814:Vmn2r70 UTSW 7 85,215,169 (GRCm39) missense probably benign 0.00
R8934:Vmn2r70 UTSW 7 85,211,188 (GRCm39) missense possibly damaging 0.87
R9225:Vmn2r70 UTSW 7 85,208,242 (GRCm39) missense probably damaging 1.00
R9322:Vmn2r70 UTSW 7 85,208,498 (GRCm39) missense possibly damaging 0.92
R9430:Vmn2r70 UTSW 7 85,215,240 (GRCm39) missense probably benign 0.10
R9477:Vmn2r70 UTSW 7 85,218,244 (GRCm39) missense possibly damaging 0.50
Z1088:Vmn2r70 UTSW 7 85,213,968 (GRCm39) missense possibly damaging 0.53
Z1176:Vmn2r70 UTSW 7 85,218,253 (GRCm39) missense probably benign 0.00
Posted On 2015-12-18