Incidental Mutation 'IGL01388:Vmn2r27'
ID 79101
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r27
Ensembl Gene ENSMUSG00000072778
Gene Name vomeronasal 2, receptor27
Synonyms EG232367
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL01388
Quality Score
Status
Chromosome 6
Chromosomal Location 124168555-124208743 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 124200791 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Serine at position 389 (P389S)
Ref Sequence ENSEMBL: ENSMUSP00000098528 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100968]
AlphaFold D3YUK6
Predicted Effect possibly damaging
Transcript: ENSMUST00000100968
AA Change: P389S

PolyPhen 2 Score 0.551 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000098528
Gene: ENSMUSG00000072778
AA Change: P389S

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:ANF_receptor 81 475 1.1e-27 PFAM
Pfam:NCD3G 519 570 1.3e-18 PFAM
Pfam:7tm_3 603 838 2.6e-50 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 T G 17: 68,160,034 (GRCm39) probably benign Het
Ces2b A C 8: 105,561,236 (GRCm39) probably benign Het
Col20a1 T A 2: 180,645,264 (GRCm39) M924K probably benign Het
Commd4 G A 9: 57,063,273 (GRCm39) probably benign Het
Ctnna3 A G 10: 63,339,886 (GRCm39) E24G possibly damaging Het
Cyp2a22 C T 7: 26,637,217 (GRCm39) R189H probably benign Het
Gapdhrt T C 14: 11,281,836 (GRCm38) D33G probably damaging Het
Gm20426 T C 6: 90,155,694 (GRCm39) probably benign Het
Gm6802 T G 12: 19,540,546 (GRCm39) noncoding transcript Het
Igkv8-21 A G 6: 70,292,153 (GRCm39) S30P probably benign Het
Lig4 A G 8: 10,023,586 (GRCm39) Y65H probably damaging Het
Mpzl1 T C 1: 165,433,336 (GRCm39) D105G probably benign Het
Myo10 A G 15: 25,736,703 (GRCm39) I451V possibly damaging Het
Nos2 G T 11: 78,848,278 (GRCm39) V1062L probably damaging Het
Oas2 A G 5: 120,886,657 (GRCm39) S170P probably damaging Het
Or1j19 G T 2: 36,677,367 (GRCm39) V277L probably benign Het
Or5w11 T A 2: 87,458,973 (GRCm39) H55Q probably benign Het
Or8b3b A T 9: 38,584,379 (GRCm39) Y120* probably null Het
Or8g37 A G 9: 39,731,298 (GRCm39) D121G probably damaging Het
Pcdh7 T C 5: 57,877,546 (GRCm39) L367P probably damaging Het
Pde3a A G 6: 141,405,464 (GRCm39) T439A probably damaging Het
Plekhm2 T C 4: 141,369,312 (GRCm39) Y124C probably damaging Het
Ppp4r4 T A 12: 103,543,108 (GRCm39) W155R probably damaging Het
Prl7c1 C A 13: 27,960,198 (GRCm39) A115S probably damaging Het
Psg25 T C 7: 18,263,590 (GRCm39) I78V possibly damaging Het
Ptpn9 T A 9: 56,944,002 (GRCm39) V292E probably benign Het
Ptprs G A 17: 56,728,261 (GRCm39) R908C probably damaging Het
Rps6ka1 C T 4: 133,599,275 (GRCm39) V51I probably damaging Het
Scube1 T C 15: 83,504,332 (GRCm39) I492V probably benign Het
Trappc2 G A X: 165,232,775 (GRCm39) probably benign Het
Ubr4 T C 4: 139,187,554 (GRCm39) V739A possibly damaging Het
Unc79 T C 12: 103,136,018 (GRCm39) probably benign Het
Wipi2 T A 5: 142,646,798 (GRCm39) F212I possibly damaging Het
Other mutations in Vmn2r27
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01285:Vmn2r27 APN 6 124,169,370 (GRCm39) missense possibly damaging 0.86
IGL01923:Vmn2r27 APN 6 124,177,484 (GRCm39) missense probably benign 0.20
IGL01954:Vmn2r27 APN 6 124,169,207 (GRCm39) missense probably damaging 1.00
IGL02105:Vmn2r27 APN 6 124,174,308 (GRCm39) splice site probably benign
IGL02586:Vmn2r27 APN 6 124,201,434 (GRCm39) nonsense probably null
IGL03130:Vmn2r27 APN 6 124,169,276 (GRCm39) missense possibly damaging 0.82
IGL03330:Vmn2r27 APN 6 124,207,139 (GRCm39) nonsense probably null
R0124:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0234:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0234:Vmn2r27 UTSW 6 124,208,578 (GRCm39) missense probably benign
R0384:Vmn2r27 UTSW 6 124,200,871 (GRCm39) missense probably benign 0.01
R0582:Vmn2r27 UTSW 6 124,201,249 (GRCm39) missense probably benign 0.02
R0733:Vmn2r27 UTSW 6 124,169,147 (GRCm39) missense probably benign 0.18
R0738:Vmn2r27 UTSW 6 124,200,661 (GRCm39) missense possibly damaging 0.48
R0835:Vmn2r27 UTSW 6 124,177,583 (GRCm39) missense probably damaging 0.99
R1183:Vmn2r27 UTSW 6 124,177,491 (GRCm39) missense probably benign
R1401:Vmn2r27 UTSW 6 124,168,591 (GRCm39) nonsense probably null
R1484:Vmn2r27 UTSW 6 124,177,474 (GRCm39) missense probably damaging 0.96
R1536:Vmn2r27 UTSW 6 124,177,649 (GRCm39) missense probably damaging 1.00
R1539:Vmn2r27 UTSW 6 124,168,730 (GRCm39) missense probably damaging 1.00
R1565:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1595:Vmn2r27 UTSW 6 124,208,574 (GRCm39) missense probably benign 0.00
R1614:Vmn2r27 UTSW 6 124,200,893 (GRCm39) missense probably benign 0.01
R1742:Vmn2r27 UTSW 6 124,177,636 (GRCm39) missense possibly damaging 0.48
R1816:Vmn2r27 UTSW 6 124,207,330 (GRCm39) nonsense probably null
R1822:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1824:Vmn2r27 UTSW 6 124,208,593 (GRCm39) missense probably benign
R1870:Vmn2r27 UTSW 6 124,201,170 (GRCm39) missense probably benign 0.11
R1942:Vmn2r27 UTSW 6 124,200,722 (GRCm39) missense probably damaging 1.00
R1962:Vmn2r27 UTSW 6 124,200,793 (GRCm39) missense possibly damaging 0.70
R2069:Vmn2r27 UTSW 6 124,201,442 (GRCm39) missense probably damaging 1.00
R2075:Vmn2r27 UTSW 6 124,177,510 (GRCm39) missense possibly damaging 0.85
R2379:Vmn2r27 UTSW 6 124,201,342 (GRCm39) missense possibly damaging 0.89
R3748:Vmn2r27 UTSW 6 124,207,351 (GRCm39) missense probably benign 0.35
R4384:Vmn2r27 UTSW 6 124,201,115 (GRCm39) missense probably benign 0.05
R4392:Vmn2r27 UTSW 6 124,207,135 (GRCm39) missense probably benign 0.01
R4758:Vmn2r27 UTSW 6 124,208,596 (GRCm39) missense possibly damaging 0.87
R5018:Vmn2r27 UTSW 6 124,201,141 (GRCm39) missense probably benign 0.02
R5235:Vmn2r27 UTSW 6 124,169,013 (GRCm39) missense probably damaging 0.99
R5718:Vmn2r27 UTSW 6 124,169,103 (GRCm39) missense possibly damaging 0.66
R5859:Vmn2r27 UTSW 6 124,177,647 (GRCm39) missense probably damaging 1.00
R5958:Vmn2r27 UTSW 6 124,208,686 (GRCm39) missense probably benign 0.00
R6044:Vmn2r27 UTSW 6 124,208,731 (GRCm39) missense probably benign
R6086:Vmn2r27 UTSW 6 124,168,958 (GRCm39) missense probably damaging 1.00
R6396:Vmn2r27 UTSW 6 124,201,125 (GRCm39) nonsense probably null
R6546:Vmn2r27 UTSW 6 124,169,369 (GRCm39) missense possibly damaging 0.49
R6746:Vmn2r27 UTSW 6 124,177,552 (GRCm39) missense possibly damaging 0.47
R6976:Vmn2r27 UTSW 6 124,201,312 (GRCm39) nonsense probably null
R7091:Vmn2r27 UTSW 6 124,200,904 (GRCm39) missense possibly damaging 0.85
R7145:Vmn2r27 UTSW 6 124,168,711 (GRCm39) missense probably benign
R7176:Vmn2r27 UTSW 6 124,168,995 (GRCm39) missense probably benign 0.01
R7382:Vmn2r27 UTSW 6 124,174,276 (GRCm39) missense probably damaging 1.00
R7482:Vmn2r27 UTSW 6 124,201,220 (GRCm39) missense probably damaging 1.00
R7853:Vmn2r27 UTSW 6 124,168,980 (GRCm39) missense probably damaging 1.00
R7859:Vmn2r27 UTSW 6 124,201,201 (GRCm39) missense probably benign 0.00
R7959:Vmn2r27 UTSW 6 124,169,040 (GRCm39) missense probably benign
R8266:Vmn2r27 UTSW 6 124,168,937 (GRCm39) missense probably benign 0.00
R8353:Vmn2r27 UTSW 6 124,169,404 (GRCm39) missense probably damaging 0.99
R8394:Vmn2r27 UTSW 6 124,168,776 (GRCm39) missense possibly damaging 0.71
R8463:Vmn2r27 UTSW 6 124,169,168 (GRCm39) missense probably damaging 1.00
R8477:Vmn2r27 UTSW 6 124,201,200 (GRCm39) missense probably benign 0.11
R8705:Vmn2r27 UTSW 6 124,207,188 (GRCm39) missense probably damaging 1.00
R8752:Vmn2r27 UTSW 6 124,201,018 (GRCm39) missense probably benign 0.00
R9109:Vmn2r27 UTSW 6 124,174,224 (GRCm39) missense possibly damaging 0.95
R9140:Vmn2r27 UTSW 6 124,169,207 (GRCm39) missense probably damaging 1.00
R9157:Vmn2r27 UTSW 6 124,201,244 (GRCm39) missense probably benign 0.09
R9431:Vmn2r27 UTSW 6 124,168,856 (GRCm39) missense probably damaging 1.00
R9477:Vmn2r27 UTSW 6 124,168,910 (GRCm39) missense probably damaging 0.99
R9758:Vmn2r27 UTSW 6 124,168,637 (GRCm39) missense possibly damaging 0.89
Z1177:Vmn2r27 UTSW 6 124,168,860 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-05