Incidental Mutation 'IGL03027:Vmn2r66'
ID 408251
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r66
Ensembl Gene ENSMUSG00000094950
Gene Name vomeronasal 2, receptor 66
Synonyms F830104D24Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # IGL03027
Quality Score
Status
Chromosome 7
Chromosomal Location 84643853-84661228 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 84644777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000122645 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000124773]
AlphaFold A0A3B2W842
Predicted Effect probably benign
Transcript: ENSMUST00000124773
SMART Domains Protein: ENSMUSP00000122645
Gene: ENSMUSG00000094950

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 463 5e-31 PFAM
Pfam:NCD3G 507 559 6e-21 PFAM
Pfam:7tm_3 589 827 3.8e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrf1 A T 17: 43,607,605 (GRCm39) Y108F probably damaging Het
Afap1 T C 5: 36,119,094 (GRCm39) I243T probably benign Het
Ano5 A G 7: 51,216,025 (GRCm39) D320G probably damaging Het
Arhgef1 T A 7: 24,623,157 (GRCm39) I423K probably damaging Het
Casp9 A G 4: 141,539,584 (GRCm39) E410G probably benign Het
Ccdc39 A C 3: 33,884,267 (GRCm39) H358Q probably benign Het
Ces5a A T 8: 94,249,742 (GRCm39) probably null Het
Clip1 A T 5: 123,759,919 (GRCm39) M935K probably benign Het
Col12a1 A G 9: 79,548,833 (GRCm39) Y2171H probably benign Het
Cyp2f2 A T 7: 26,831,996 (GRCm39) N417I possibly damaging Het
Dock3 G A 9: 106,870,677 (GRCm39) P579L probably damaging Het
Dock7 T C 4: 98,866,164 (GRCm39) M1209V probably benign Het
Dock7 T C 4: 98,958,450 (GRCm39) T334A possibly damaging Het
Dst A T 1: 34,225,106 (GRCm39) I1171F possibly damaging Het
Eya1 G T 1: 14,241,190 (GRCm39) H576N probably damaging Het
Fam117a A G 11: 95,268,399 (GRCm39) T267A probably benign Het
Fam43a C T 16: 30,419,922 (GRCm39) R169C probably damaging Het
Gabra6 T C 11: 42,205,980 (GRCm39) H291R probably damaging Het
Gm7145 T C 1: 117,895,417 (GRCm39) S27P probably benign Het
Gpt C T 15: 76,582,289 (GRCm39) probably benign Het
Grip2 A G 6: 91,755,852 (GRCm39) I586T probably benign Het
Hif1a C T 12: 73,987,251 (GRCm39) P448L probably benign Het
Hmcn1 C T 1: 150,684,290 (GRCm39) V427I probably benign Het
Ipo8 C A 6: 148,678,737 (GRCm39) V954L probably benign Het
Kdm5a G T 6: 120,351,951 (GRCm39) probably null Het
Klhl36 T A 8: 120,603,229 (GRCm39) S495T probably benign Het
Lpar5 T A 6: 125,059,203 (GRCm39) L308Q probably damaging Het
Lrp2 T G 2: 69,367,897 (GRCm39) D205A probably benign Het
Lrriq1 A G 10: 103,063,057 (GRCm39) I83T probably benign Het
Mapk8ip2 A T 15: 89,342,310 (GRCm39) D507V probably damaging Het
Mical1 T C 10: 41,355,501 (GRCm39) probably benign Het
Myef2 T A 2: 124,930,954 (GRCm39) H539L possibly damaging Het
Myh7 T C 14: 55,221,007 (GRCm39) E972G probably damaging Het
Naip5 A G 13: 100,359,524 (GRCm39) Y571H probably benign Het
Nfasc T A 1: 132,538,207 (GRCm39) N478I probably damaging Het
Or6c1b A G 10: 129,272,780 (GRCm39) Y33C probably damaging Het
Pde2a A T 7: 101,130,627 (GRCm39) Q89L probably benign Het
Ppard C A 17: 28,518,765 (GRCm39) T422K possibly damaging Het
Ppp1r13b G T 12: 111,796,830 (GRCm39) Y904* probably null Het
Ptx4 T A 17: 25,344,022 (GRCm39) I424K possibly damaging Het
Rab19 A G 6: 39,360,927 (GRCm39) D25G probably damaging Het
Rbl2 T A 8: 91,805,534 (GRCm39) I197N possibly damaging Het
Rttn A G 18: 88,997,814 (GRCm39) D273G probably damaging Het
Sec16a G A 2: 26,313,601 (GRCm39) R1920C probably benign Het
Sec23b A T 2: 144,429,465 (GRCm39) N731I possibly damaging Het
Serpinb9d G A 13: 33,386,698 (GRCm39) W255* probably null Het
Sim2 G A 16: 93,910,351 (GRCm39) probably benign Het
Tbl3 T C 17: 24,920,167 (GRCm39) probably null Het
Tmem176b C T 6: 48,812,573 (GRCm39) A131T probably damaging Het
Tmem181a T A 17: 6,348,494 (GRCm39) V332D probably damaging Het
Trgc1 G T 13: 19,398,563 (GRCm39) G97* probably null Het
Tuba3b T A 6: 145,565,117 (GRCm39) L195Q probably damaging Het
Ubc A T 5: 125,464,565 (GRCm39) V254D probably damaging Het
Ube4b G T 4: 149,465,734 (GRCm39) P239T probably damaging Het
Vars1 G T 17: 35,232,663 (GRCm39) M862I probably damaging Het
Wdr59 G A 8: 112,188,824 (GRCm39) A720V probably damaging Het
Zfhx3 G A 8: 109,519,820 (GRCm39) R314Q probably damaging Het
Other mutations in Vmn2r66
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00321:Vmn2r66 APN 7 84,656,299 (GRCm39) missense probably benign
IGL01562:Vmn2r66 APN 7 84,656,495 (GRCm39) missense probably benign 0.03
IGL01689:Vmn2r66 APN 7 84,657,033 (GRCm39) missense probably damaging 1.00
IGL02237:Vmn2r66 APN 7 84,643,908 (GRCm39) missense probably benign
IGL02415:Vmn2r66 APN 7 84,656,020 (GRCm39) missense probably damaging 0.97
IGL02439:Vmn2r66 APN 7 84,654,455 (GRCm39) splice site probably benign
IGL02545:Vmn2r66 APN 7 84,655,798 (GRCm39) missense possibly damaging 0.50
IGL02708:Vmn2r66 APN 7 84,655,796 (GRCm39) missense probably benign 0.00
IGL02794:Vmn2r66 APN 7 84,644,623 (GRCm39) missense probably benign 0.00
IGL02885:Vmn2r66 APN 7 84,644,723 (GRCm39) missense probably benign 0.00
IGL02975:Vmn2r66 APN 7 84,656,182 (GRCm39) missense probably damaging 0.98
IGL03081:Vmn2r66 APN 7 84,657,138 (GRCm39) missense probably benign
PIT4131001:Vmn2r66 UTSW 7 84,644,301 (GRCm39) missense probably damaging 1.00
R0098:Vmn2r66 UTSW 7 84,654,965 (GRCm39) missense probably damaging 1.00
R0504:Vmn2r66 UTSW 7 84,656,023 (GRCm39) missense probably damaging 0.99
R0557:Vmn2r66 UTSW 7 84,643,972 (GRCm39) missense probably damaging 1.00
R0617:Vmn2r66 UTSW 7 84,644,484 (GRCm39) missense probably benign 0.02
R0883:Vmn2r66 UTSW 7 84,657,070 (GRCm39) missense probably benign
R1159:Vmn2r66 UTSW 7 84,644,613 (GRCm39) missense probably benign 0.44
R1168:Vmn2r66 UTSW 7 84,656,062 (GRCm39) missense possibly damaging 0.46
R1172:Vmn2r66 UTSW 7 84,654,799 (GRCm39) missense probably benign 0.04
R1175:Vmn2r66 UTSW 7 84,654,799 (GRCm39) missense probably benign 0.04
R1538:Vmn2r66 UTSW 7 84,644,166 (GRCm39) missense possibly damaging 0.84
R1658:Vmn2r66 UTSW 7 84,656,955 (GRCm39) missense probably benign 0.07
R1937:Vmn2r66 UTSW 7 84,644,344 (GRCm39) missense probably damaging 0.99
R1989:Vmn2r66 UTSW 7 84,661,201 (GRCm39) missense probably benign 0.01
R2698:Vmn2r66 UTSW 7 84,644,607 (GRCm39) missense probably damaging 1.00
R2890:Vmn2r66 UTSW 7 84,661,027 (GRCm39) splice site probably null
R3686:Vmn2r66 UTSW 7 84,644,397 (GRCm39) missense probably damaging 0.96
R4152:Vmn2r66 UTSW 7 84,654,800 (GRCm39) missense probably benign 0.08
R4500:Vmn2r66 UTSW 7 84,657,162 (GRCm39) missense probably damaging 1.00
R4618:Vmn2r66 UTSW 7 84,644,296 (GRCm39) missense possibly damaging 0.62
R4656:Vmn2r66 UTSW 7 84,661,204 (GRCm39) missense possibly damaging 0.87
R4668:Vmn2r66 UTSW 7 84,643,905 (GRCm39) missense probably damaging 1.00
R4942:Vmn2r66 UTSW 7 84,656,980 (GRCm39) missense probably damaging 1.00
R5163:Vmn2r66 UTSW 7 84,656,017 (GRCm39) missense probably benign 0.01
R5223:Vmn2r66 UTSW 7 84,657,093 (GRCm39) missense probably benign
R5377:Vmn2r66 UTSW 7 84,656,026 (GRCm39) missense probably damaging 0.99
R5512:Vmn2r66 UTSW 7 84,657,149 (GRCm39) missense probably damaging 1.00
R5611:Vmn2r66 UTSW 7 84,654,951 (GRCm39) nonsense probably null
R5749:Vmn2r66 UTSW 7 84,655,979 (GRCm39) nonsense probably null
R6131:Vmn2r66 UTSW 7 84,644,224 (GRCm39) missense probably damaging 1.00
R6183:Vmn2r66 UTSW 7 84,644,766 (GRCm39) missense possibly damaging 0.81
R6509:Vmn2r66 UTSW 7 84,656,054 (GRCm39) missense probably benign 0.12
R6930:Vmn2r66 UTSW 7 84,661,216 (GRCm39) missense possibly damaging 0.80
R6992:Vmn2r66 UTSW 7 84,654,436 (GRCm39) missense possibly damaging 0.90
R7015:Vmn2r66 UTSW 7 84,644,766 (GRCm39) missense possibly damaging 0.81
R7302:Vmn2r66 UTSW 7 84,654,423 (GRCm39) missense probably benign 0.00
R7516:Vmn2r66 UTSW 7 84,661,176 (GRCm39) missense possibly damaging 0.51
R7763:Vmn2r66 UTSW 7 84,654,909 (GRCm39) missense probably benign 0.01
R7814:Vmn2r66 UTSW 7 84,656,472 (GRCm39) missense probably benign 0.02
R8077:Vmn2r66 UTSW 7 84,656,093 (GRCm39) missense probably benign
R8307:Vmn2r66 UTSW 7 84,656,270 (GRCm39) missense probably benign
R8315:Vmn2r66 UTSW 7 84,643,932 (GRCm39) missense possibly damaging 0.90
R8490:Vmn2r66 UTSW 7 84,654,794 (GRCm39) critical splice donor site probably null
R8511:Vmn2r66 UTSW 7 84,656,026 (GRCm39) missense probably damaging 0.99
R8781:Vmn2r66 UTSW 7 84,644,355 (GRCm39) nonsense probably null
R8812:Vmn2r66 UTSW 7 84,654,893 (GRCm39) missense probably damaging 0.99
R9203:Vmn2r66 UTSW 7 84,654,950 (GRCm39) missense probably benign 0.01
R9277:Vmn2r66 UTSW 7 84,661,164 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02