Incidental Mutation 'IGL02263:Vmn2r7'
ID 286807
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r7
Ensembl Gene ENSMUSG00000116028
Gene Name vomeronasal 2, receptor 7
Synonyms 4933425M15Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.115) question?
Stock # IGL02263
Quality Score
Status
Chromosome 3
Chromosomal Location 64598081-64627023 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 64598868 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 654 (V654G)
Ref Sequence ENSEMBL: ENSMUSP00000124192 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000161972] [ENSMUST00000168072]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000161972
AA Change: V654G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000124192
Gene: ENSMUSG00000062200
AA Change: V654G

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 90 507 3.8e-77 PFAM
Pfam:NCD3G 549 602 3.4e-17 PFAM
Pfam:7tm_3 635 869 1.1e-47 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000168072
AA Change: V563G

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000131220
Gene: ENSMUSG00000116028
AA Change: V563G

DomainStartEndE-ValueType
Pfam:ANF_receptor 1 416 5.1e-72 PFAM
Pfam:Peripla_BP_6 63 245 6.1e-10 PFAM
Pfam:NCD3G 458 511 1.8e-17 PFAM
Pfam:7tm_3 542 779 4.3e-76 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000177146
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aff3 A G 1: 38,574,680 (GRCm39) V100A probably damaging Het
Agmo T A 12: 37,407,696 (GRCm39) N193K probably damaging Het
Dnah8 A G 17: 30,948,139 (GRCm39) I1910V probably benign Het
Dsg2 T A 18: 20,723,077 (GRCm39) S368T possibly damaging Het
Eif2ak4 A G 2: 118,292,259 (GRCm39) T1270A probably benign Het
Ina T C 19: 47,003,926 (GRCm39) S245P probably damaging Het
Katnb1 A G 8: 95,816,703 (GRCm39) K96R probably damaging Het
Kcnj4 A G 15: 79,369,988 (GRCm39) probably benign Het
Kcnn3 A G 3: 89,568,525 (GRCm39) H601R possibly damaging Het
Lrrc25 C A 8: 71,070,472 (GRCm39) F84L probably benign Het
Ltb A G 17: 35,414,977 (GRCm39) Y259C probably damaging Het
Macc1 T G 12: 119,409,752 (GRCm39) N173K possibly damaging Het
Med17 A T 9: 15,178,772 (GRCm39) N466K probably damaging Het
Ncoa2 A T 1: 13,244,987 (GRCm39) N570K probably damaging Het
Or52ae9 A T 7: 103,390,262 (GRCm39) F62I probably damaging Het
Or5w1 A T 2: 87,486,543 (GRCm39) C241S probably damaging Het
Or8k20 T A 2: 86,106,546 (GRCm39) Y95F probably benign Het
Plb1 T C 5: 32,478,692 (GRCm39) probably benign Het
Ptprk G A 10: 27,951,110 (GRCm39) V12I unknown Het
Rabggta G A 14: 55,956,418 (GRCm39) probably benign Het
Slc41a2 A G 10: 83,149,364 (GRCm39) V193A possibly damaging Het
Thbs1 A G 2: 117,950,361 (GRCm39) N665D probably benign Het
Tm9sf1 T C 14: 55,880,392 (GRCm39) T2A possibly damaging Het
Traf7 C A 17: 24,732,020 (GRCm39) C193F possibly damaging Het
Vmn1r91 A G 7: 19,835,768 (GRCm39) D229G probably benign Het
Other mutations in Vmn2r7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00961:Vmn2r7 APN 3 64,623,234 (GRCm39) missense possibly damaging 0.60
IGL01762:Vmn2r7 APN 3 64,598,856 (GRCm39) missense probably benign 0.39
IGL01903:Vmn2r7 APN 3 64,626,864 (GRCm39) missense probably benign 0.00
IGL02458:Vmn2r7 APN 3 64,600,446 (GRCm39) missense probably damaging 0.97
IGL02593:Vmn2r7 APN 3 64,600,443 (GRCm39) missense probably damaging 1.00
IGL02797:Vmn2r7 APN 3 64,598,666 (GRCm39) missense possibly damaging 0.80
IGL03047:Vmn2r7 UTSW 3 64,614,639 (GRCm39) missense possibly damaging 0.81
PIT4504001:Vmn2r7 UTSW 3 64,623,397 (GRCm39) missense probably benign 0.01
R0193:Vmn2r7 UTSW 3 64,598,460 (GRCm39) missense probably damaging 1.00
R0329:Vmn2r7 UTSW 3 64,598,439 (GRCm39) missense probably damaging 1.00
R0609:Vmn2r7 UTSW 3 64,623,900 (GRCm39) missense probably benign 0.44
R0735:Vmn2r7 UTSW 3 64,623,788 (GRCm39) missense probably benign 0.02
R0941:Vmn2r7 UTSW 3 64,624,000 (GRCm39) missense probably benign
R1065:Vmn2r7 UTSW 3 64,614,559 (GRCm39) missense possibly damaging 0.82
R1378:Vmn2r7 UTSW 3 64,599,025 (GRCm39) missense possibly damaging 0.59
R1445:Vmn2r7 UTSW 3 64,632,223 (GRCm39) missense probably benign 0.01
R1506:Vmn2r7 UTSW 3 64,614,500 (GRCm39) missense probably benign
R1509:Vmn2r7 UTSW 3 64,623,881 (GRCm39) nonsense probably null
R1519:Vmn2r7 UTSW 3 64,623,876 (GRCm39) missense possibly damaging 0.95
R1706:Vmn2r7 UTSW 3 64,598,880 (GRCm39) missense possibly damaging 0.79
R2113:Vmn2r7 UTSW 3 64,599,025 (GRCm39) missense possibly damaging 0.59
R3725:Vmn2r7 UTSW 3 64,632,412 (GRCm39) missense possibly damaging 0.65
R3874:Vmn2r7 UTSW 3 64,627,032 (GRCm39) missense possibly damaging 0.69
R3902:Vmn2r7 UTSW 3 64,626,937 (GRCm39) missense possibly damaging 0.46
R4084:Vmn2r7 UTSW 3 64,600,414 (GRCm39) missense probably benign 0.08
R4117:Vmn2r7 UTSW 3 64,623,138 (GRCm39) intron probably benign
R4333:Vmn2r7 UTSW 3 64,598,199 (GRCm39) missense probably damaging 1.00
R4551:Vmn2r7 UTSW 3 64,598,110 (GRCm39) missense possibly damaging 0.86
R4643:Vmn2r7 UTSW 3 64,623,825 (GRCm39) missense probably damaging 1.00
R4654:Vmn2r7 UTSW 3 64,626,864 (GRCm39) missense probably benign 0.00
R5091:Vmn2r7 UTSW 3 64,598,205 (GRCm39) missense possibly damaging 0.63
R5109:Vmn2r7 UTSW 3 64,598,088 (GRCm39) missense probably null 0.84
R5372:Vmn2r7 UTSW 3 64,623,745 (GRCm39) missense probably damaging 1.00
R5415:Vmn2r7 UTSW 3 64,623,658 (GRCm39) missense probably benign 0.07
R5740:Vmn2r7 UTSW 3 64,614,654 (GRCm39) missense probably benign
R5977:Vmn2r7 UTSW 3 64,623,464 (GRCm39) nonsense probably null
R6019:Vmn2r7 UTSW 3 64,623,643 (GRCm39) missense probably damaging 1.00
R6058:Vmn2r7 UTSW 3 64,632,436 (GRCm39) missense probably benign 0.00
R6139:Vmn2r7 UTSW 3 64,623,339 (GRCm39) missense probably damaging 1.00
R6696:Vmn2r7 UTSW 3 64,614,495 (GRCm39) missense probably benign 0.01
R6887:Vmn2r7 UTSW 3 64,598,248 (GRCm39) missense probably damaging 1.00
R6918:Vmn2r7 UTSW 3 64,598,760 (GRCm39) missense probably benign 0.03
R6949:Vmn2r7 UTSW 3 64,598,542 (GRCm39) missense probably damaging 0.99
R6980:Vmn2r7 UTSW 3 64,623,987 (GRCm39) missense possibly damaging 0.67
R7196:Vmn2r7 UTSW 3 64,623,198 (GRCm39) missense probably benign 0.00
R7286:Vmn2r7 UTSW 3 64,598,301 (GRCm39) missense probably benign 0.00
R7455:Vmn2r7 UTSW 3 64,624,014 (GRCm39) missense probably benign
R7557:Vmn2r7 UTSW 3 64,632,394 (GRCm39) missense probably benign
R7864:Vmn2r7 UTSW 3 64,598,947 (GRCm39) missense probably benign 0.10
R8046:Vmn2r7 UTSW 3 64,614,479 (GRCm39) missense probably damaging 1.00
R8068:Vmn2r7 UTSW 3 64,623,507 (GRCm39) missense probably benign 0.01
R8252:Vmn2r7 UTSW 3 64,600,527 (GRCm39) missense probably benign 0.00
R8814:Vmn2r7 UTSW 3 64,623,984 (GRCm39) missense probably benign 0.14
R9497:Vmn2r7 UTSW 3 64,614,474 (GRCm39) missense probably benign 0.04
R9722:Vmn2r7 UTSW 3 64,598,407 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16