Incidental Mutation 'IGL01398:Vmn2r51'
ID 79522
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r51
Ensembl Gene ENSMUSG00000058685
Gene Name vomeronasal 2, receptor 51
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # IGL01398
Quality Score
Status
Chromosome 7
Chromosomal Location 9821125-9839586 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 9836341 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Lysine at position 147 (E147K)
Ref Sequence ENSEMBL: ENSMUSP00000092459 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094863]
AlphaFold L7N215
Predicted Effect probably benign
Transcript: ENSMUST00000094863
AA Change: E147K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000092459
Gene: ENSMUSG00000058685
AA Change: E147K

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 2.4e-31 PFAM
Pfam:NCD3G 512 565 8.1e-21 PFAM
Pfam:7tm_3 598 833 2.7e-54 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acap1 T C 11: 69,772,548 (GRCm39) D521G probably damaging Het
Apol11b G A 15: 77,522,219 (GRCm39) T26M probably damaging Het
Best2 T A 8: 85,735,956 (GRCm39) Y326F probably damaging Het
Clca3a1 T C 3: 144,722,512 (GRCm39) T287A possibly damaging Het
Cyp26a1 C T 19: 37,686,395 (GRCm39) T13I probably damaging Het
Dhcr7 T C 7: 143,395,056 (GRCm39) S188P probably damaging Het
Eml3 T G 19: 8,911,598 (GRCm39) probably benign Het
Faf1 A T 4: 109,593,793 (GRCm39) I124F probably damaging Het
Fkbp9 T A 6: 56,837,790 (GRCm39) probably benign Het
Foxq1 G A 13: 31,743,434 (GRCm39) D179N probably damaging Het
Frem1 C T 4: 82,868,599 (GRCm39) V1443M possibly damaging Het
Gpnmb T A 6: 49,027,365 (GRCm39) M363K probably benign Het
Grm3 T C 5: 9,535,762 (GRCm39) probably benign Het
Ints3 A G 3: 90,300,130 (GRCm39) L929P probably damaging Het
Myh11 T A 16: 14,019,964 (GRCm39) I1823F probably damaging Het
Nudt9 T C 5: 104,212,979 (GRCm39) *351Q probably null Het
Or2ak6 A T 11: 58,592,593 (GRCm39) H22L probably benign Het
Or4c107 C T 2: 88,789,193 (GRCm39) P128S probably damaging Het
Or8k38 A T 2: 86,488,032 (GRCm39) F257I probably damaging Het
Pgr15l C T X: 96,121,785 (GRCm39) T392I probably benign Het
Sdk1 C A 5: 141,923,332 (GRCm39) L318I probably benign Het
Sult1c2 C A 17: 54,269,180 (GRCm39) V279L possibly damaging Het
Tek T C 4: 94,738,014 (GRCm39) I688T probably damaging Het
Telo2 A T 17: 25,324,748 (GRCm39) D477E probably benign Het
Ubr3 T A 2: 69,789,997 (GRCm39) Y884N probably damaging Het
Upf3a C A 8: 13,836,221 (GRCm39) H92Q probably damaging Het
Vps54 A G 11: 21,245,403 (GRCm39) probably benign Het
Zdhhc14 T C 17: 5,762,738 (GRCm39) I214T possibly damaging Het
Other mutations in Vmn2r51
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01574:Vmn2r51 APN 7 9,836,381 (GRCm39) missense probably damaging 1.00
IGL01743:Vmn2r51 APN 7 9,834,154 (GRCm39) missense probably damaging 0.98
IGL01820:Vmn2r51 APN 7 9,839,409 (GRCm39) missense probably damaging 1.00
IGL02563:Vmn2r51 APN 7 9,834,243 (GRCm39) missense probably benign 0.00
IGL02825:Vmn2r51 APN 7 9,832,046 (GRCm39) splice site probably benign
IGL02834:Vmn2r51 APN 7 9,832,063 (GRCm39) nonsense probably null
R0617:Vmn2r51 UTSW 7 9,834,396 (GRCm39) missense possibly damaging 0.65
R0967:Vmn2r51 UTSW 7 9,834,012 (GRCm39) missense probably damaging 0.97
R1465:Vmn2r51 UTSW 7 9,834,249 (GRCm39) missense probably damaging 1.00
R1465:Vmn2r51 UTSW 7 9,834,249 (GRCm39) missense probably damaging 1.00
R1559:Vmn2r51 UTSW 7 9,836,373 (GRCm39) missense possibly damaging 0.87
R1559:Vmn2r51 UTSW 7 9,836,372 (GRCm39) missense possibly damaging 0.58
R1598:Vmn2r51 UTSW 7 9,839,432 (GRCm39) missense probably benign
R1754:Vmn2r51 UTSW 7 9,833,873 (GRCm39) missense probably benign 0.04
R1836:Vmn2r51 UTSW 7 9,832,091 (GRCm39) nonsense probably null
R1836:Vmn2r51 UTSW 7 9,832,090 (GRCm39) nonsense probably null
R3151:Vmn2r51 UTSW 7 9,833,968 (GRCm39) missense probably damaging 1.00
R4566:Vmn2r51 UTSW 7 9,836,341 (GRCm39) missense probably benign
R4933:Vmn2r51 UTSW 7 9,832,247 (GRCm39) missense probably damaging 1.00
R5004:Vmn2r51 UTSW 7 9,821,932 (GRCm39) missense probably benign
R5050:Vmn2r51 UTSW 7 9,834,349 (GRCm39) missense probably damaging 0.99
R5510:Vmn2r51 UTSW 7 9,836,545 (GRCm39) missense possibly damaging 0.95
R5559:Vmn2r51 UTSW 7 9,826,128 (GRCm39) missense probably damaging 1.00
R6127:Vmn2r51 UTSW 7 9,839,558 (GRCm39) missense probably damaging 1.00
R6154:Vmn2r51 UTSW 7 9,821,921 (GRCm39) missense possibly damaging 0.74
R6304:Vmn2r51 UTSW 7 9,832,164 (GRCm39) missense probably benign 0.00
R6370:Vmn2r51 UTSW 7 9,832,143 (GRCm39) missense probably damaging 1.00
R6471:Vmn2r51 UTSW 7 9,836,510 (GRCm39) missense possibly damaging 0.48
R6800:Vmn2r51 UTSW 7 9,832,191 (GRCm39) missense probably damaging 0.99
R6883:Vmn2r51 UTSW 7 9,834,025 (GRCm39) missense possibly damaging 0.75
R7191:Vmn2r51 UTSW 7 9,834,480 (GRCm39) missense probably null 1.00
R7246:Vmn2r51 UTSW 7 9,836,428 (GRCm39) missense probably benign 0.00
R8939:Vmn2r51 UTSW 7 9,833,953 (GRCm39) missense possibly damaging 0.85
R9154:Vmn2r51 UTSW 7 9,839,480 (GRCm39) missense probably damaging 0.96
R9428:Vmn2r51 UTSW 7 9,833,712 (GRCm39) critical splice donor site probably benign
R9451:Vmn2r51 UTSW 7 9,833,816 (GRCm39) missense probably damaging 1.00
R9729:Vmn2r51 UTSW 7 9,839,479 (GRCm39) missense probably benign 0.00
R9767:Vmn2r51 UTSW 7 9,839,407 (GRCm39) missense probably benign 0.09
Z1176:Vmn2r51 UTSW 7 9,833,835 (GRCm39) missense probably benign 0.12
Z1176:Vmn2r51 UTSW 7 9,821,984 (GRCm39) missense possibly damaging 0.76
Posted On 2013-11-05