Incidental Mutation 'IGL01346:Vmn2r67'
ID 75036
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r67
Ensembl Gene ENSMUSG00000095664
Gene Name vomeronasal 2, receptor 67
Synonyms EG620672
Accession Numbers
Essential gene? Probably non essential (E-score: 0.111) question?
Stock # IGL01346
Quality Score
Status
Chromosome 7
Chromosomal Location 84785448-84805110 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 84786127 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 626 (L626P)
Ref Sequence ENSEMBL: ENSMUSP00000126007 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168730]
AlphaFold K7N6T2
Predicted Effect probably damaging
Transcript: ENSMUST00000168730
AA Change: L626P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000126007
Gene: ENSMUSG00000095664
AA Change: L626P

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:ANF_receptor 77 464 2.1e-31 PFAM
Pfam:NCD3G 507 559 4.8e-19 PFAM
Pfam:7tm_3 590 827 1.4e-53 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3300002I08Rik A G 2: 150,152,980 (GRCm39) V135A unknown Het
Cnot4 A T 6: 35,047,183 (GRCm39) I143N probably damaging Het
Cnot6l A T 5: 96,234,105 (GRCm39) M302K probably damaging Het
Dmxl2 T C 9: 54,322,759 (GRCm39) T1542A probably damaging Het
Dnaaf9 A G 2: 130,633,766 (GRCm39) probably benign Het
Dnhd1 T C 7: 105,363,116 (GRCm39) S3893P probably benign Het
Duox2 A T 2: 122,117,683 (GRCm39) probably benign Het
Dusp1 T C 17: 26,725,295 (GRCm39) N355D probably benign Het
Fam76b T C 9: 13,741,046 (GRCm39) C60R probably damaging Het
Gnptab G A 10: 88,272,041 (GRCm39) V944I possibly damaging Het
Gys1 A G 7: 45,091,961 (GRCm39) Y249C probably damaging Het
Ift88 A T 14: 57,681,862 (GRCm39) E215D probably damaging Het
Kcnu1 T C 8: 26,424,551 (GRCm39) probably benign Het
Lmln C A 16: 32,937,490 (GRCm39) N618K probably benign Het
Lrrc75a T C 11: 62,496,813 (GRCm39) T250A probably damaging Het
Mpp4 A G 1: 59,164,719 (GRCm39) S435P probably damaging Het
Myo1c T A 11: 75,563,076 (GRCm39) V1036E probably damaging Het
Nlrp12 T G 7: 3,289,316 (GRCm39) T399P probably damaging Het
Or2y16 A G 11: 49,335,595 (GRCm39) R306G probably benign Het
Or4c118 A G 2: 88,974,575 (GRCm39) F264S possibly damaging Het
Parp8 A T 13: 117,031,600 (GRCm39) C332S possibly damaging Het
Pdcd11 G A 19: 47,098,053 (GRCm39) V780I probably benign Het
Plekha5 A G 6: 140,480,292 (GRCm39) probably benign Het
Ppt1 T A 4: 122,737,848 (GRCm39) I62K probably damaging Het
Proser3 T C 7: 30,249,071 (GRCm39) N7S probably benign Het
Ptk2b A G 14: 66,414,567 (GRCm39) L311P possibly damaging Het
Rasal2 T C 1: 156,988,786 (GRCm39) N706S probably benign Het
Ripk2 A G 4: 16,132,775 (GRCm39) probably null Het
Setx T A 2: 29,034,821 (GRCm39) H435Q probably damaging Het
Smurf2 T A 11: 106,721,741 (GRCm39) probably benign Het
Snx32 A G 19: 5,547,764 (GRCm39) L182P possibly damaging Het
Stpg2 A G 3: 139,125,635 (GRCm39) probably benign Het
Taar2 A G 10: 23,816,997 (GRCm39) Y179C probably damaging Het
Tenm2 G A 11: 35,918,232 (GRCm39) R1843* probably null Het
Tmco4 T C 4: 138,748,260 (GRCm39) I280T probably damaging Het
Tuba4a C A 1: 75,193,921 (GRCm39) C46F probably damaging Het
Ubr1 A G 2: 120,703,603 (GRCm39) probably null Het
Vldlr A T 19: 27,217,081 (GRCm39) I45L possibly damaging Het
Vmn2r120 C A 17: 57,852,232 (GRCm39) G28V probably benign Het
Vmn2r37 C A 7: 9,209,680 (GRCm39) V611L probably benign Het
Wdr19 C T 5: 65,379,082 (GRCm39) probably benign Het
Zfp595 T A 13: 67,464,749 (GRCm39) K505* probably null Het
Other mutations in Vmn2r67
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00096:Vmn2r67 APN 7 84,801,138 (GRCm39) missense probably damaging 1.00
IGL01373:Vmn2r67 APN 7 84,785,834 (GRCm39) missense probably benign 0.10
IGL01674:Vmn2r67 APN 7 84,785,651 (GRCm39) missense probably damaging 1.00
IGL01978:Vmn2r67 APN 7 84,800,649 (GRCm39) critical splice donor site probably null
IGL02013:Vmn2r67 APN 7 84,800,863 (GRCm39) missense probably benign 0.09
IGL02115:Vmn2r67 APN 7 84,800,787 (GRCm39) missense probably damaging 0.99
IGL02250:Vmn2r67 APN 7 84,805,008 (GRCm39) missense probably benign
IGL02252:Vmn2r67 APN 7 84,805,008 (GRCm39) missense probably benign
IGL02328:Vmn2r67 APN 7 84,799,898 (GRCm39) missense probably benign 0.41
IGL02740:Vmn2r67 APN 7 84,785,818 (GRCm39) missense probably damaging 1.00
IGL02940:Vmn2r67 APN 7 84,785,951 (GRCm39) missense probably benign 0.07
IGL03237:Vmn2r67 APN 7 84,799,118 (GRCm39) missense probably damaging 1.00
R0512:Vmn2r67 UTSW 7 84,799,900 (GRCm39) missense probably damaging 1.00
R1029:Vmn2r67 UTSW 7 84,785,974 (GRCm39) missense probably damaging 1.00
R1193:Vmn2r67 UTSW 7 84,800,653 (GRCm39) missense probably damaging 0.98
R1282:Vmn2r67 UTSW 7 84,785,932 (GRCm39) missense probably benign
R1416:Vmn2r67 UTSW 7 84,800,824 (GRCm39) missense probably benign 0.06
R1429:Vmn2r67 UTSW 7 84,802,031 (GRCm39) missense possibly damaging 0.65
R1462:Vmn2r67 UTSW 7 84,805,046 (GRCm39) missense probably benign 0.00
R1462:Vmn2r67 UTSW 7 84,805,046 (GRCm39) missense probably benign 0.00
R1970:Vmn2r67 UTSW 7 84,801,013 (GRCm39) missense probably benign
R2229:Vmn2r67 UTSW 7 84,801,250 (GRCm39) missense probably benign 0.21
R2246:Vmn2r67 UTSW 7 84,785,764 (GRCm39) missense probably damaging 1.00
R2262:Vmn2r67 UTSW 7 84,786,182 (GRCm39) missense probably damaging 0.96
R2398:Vmn2r67 UTSW 7 84,785,921 (GRCm39) missense probably damaging 1.00
R4249:Vmn2r67 UTSW 7 84,799,722 (GRCm39) splice site probably null
R4666:Vmn2r67 UTSW 7 84,799,831 (GRCm39) missense probably benign
R4669:Vmn2r67 UTSW 7 84,799,732 (GRCm39) missense probably benign 0.11
R4966:Vmn2r67 UTSW 7 84,785,593 (GRCm39) missense probably damaging 1.00
R5264:Vmn2r67 UTSW 7 84,801,453 (GRCm39) missense probably damaging 1.00
R5296:Vmn2r67 UTSW 7 84,786,230 (GRCm39) missense probably damaging 1.00
R5327:Vmn2r67 UTSW 7 84,785,698 (GRCm39) missense probably damaging 1.00
R5401:Vmn2r67 UTSW 7 84,785,765 (GRCm39) missense probably damaging 1.00
R5510:Vmn2r67 UTSW 7 84,801,023 (GRCm39) missense probably benign 0.39
R5574:Vmn2r67 UTSW 7 84,801,099 (GRCm39) missense probably benign 0.00
R5643:Vmn2r67 UTSW 7 84,799,151 (GRCm39) nonsense probably null
R5914:Vmn2r67 UTSW 7 84,801,044 (GRCm39) missense probably damaging 1.00
R6248:Vmn2r67 UTSW 7 84,799,768 (GRCm39) missense probably damaging 0.99
R6291:Vmn2r67 UTSW 7 84,799,142 (GRCm39) missense possibly damaging 0.88
R6309:Vmn2r67 UTSW 7 84,801,124 (GRCm39) missense probably benign
R6442:Vmn2r67 UTSW 7 84,805,046 (GRCm39) missense possibly damaging 0.82
R6665:Vmn2r67 UTSW 7 84,785,900 (GRCm39) missense probably benign 0.07
R6701:Vmn2r67 UTSW 7 84,802,023 (GRCm39) missense probably damaging 1.00
R6848:Vmn2r67 UTSW 7 84,801,840 (GRCm39) missense probably benign 0.00
R6852:Vmn2r67 UTSW 7 84,801,361 (GRCm39) missense probably damaging 0.99
R6991:Vmn2r67 UTSW 7 84,804,953 (GRCm39) missense possibly damaging 0.55
R7143:Vmn2r67 UTSW 7 84,801,846 (GRCm39) missense probably benign
R7197:Vmn2r67 UTSW 7 84,785,774 (GRCm39) missense possibly damaging 0.77
R7393:Vmn2r67 UTSW 7 84,805,086 (GRCm39) missense probably null 0.87
R7420:Vmn2r67 UTSW 7 84,785,944 (GRCm39) missense possibly damaging 0.52
R7622:Vmn2r67 UTSW 7 84,785,662 (GRCm39) missense probably damaging 1.00
R7664:Vmn2r67 UTSW 7 84,805,019 (GRCm39) missense probably benign 0.21
R7665:Vmn2r67 UTSW 7 84,801,196 (GRCm39) nonsense probably null
R7896:Vmn2r67 UTSW 7 84,785,920 (GRCm39) missense probably damaging 1.00
R7913:Vmn2r67 UTSW 7 84,801,036 (GRCm39) missense possibly damaging 0.87
R8026:Vmn2r67 UTSW 7 84,785,924 (GRCm39) missense probably damaging 1.00
R8114:Vmn2r67 UTSW 7 84,805,097 (GRCm39) missense probably benign 0.01
R8317:Vmn2r67 UTSW 7 84,785,834 (GRCm39) missense probably benign 0.10
R8363:Vmn2r67 UTSW 7 84,804,969 (GRCm39) missense probably benign 0.00
R8421:Vmn2r67 UTSW 7 84,785,893 (GRCm39) missense probably damaging 0.98
R8444:Vmn2r67 UTSW 7 84,785,854 (GRCm39) missense probably benign 0.01
R8751:Vmn2r67 UTSW 7 84,801,450 (GRCm39) missense probably benign 0.01
R8810:Vmn2r67 UTSW 7 84,786,346 (GRCm39) missense probably damaging 1.00
R8811:Vmn2r67 UTSW 7 84,799,895 (GRCm39) missense probably damaging 0.98
R9215:Vmn2r67 UTSW 7 84,802,008 (GRCm39) missense probably benign 0.00
R9342:Vmn2r67 UTSW 7 84,785,788 (GRCm39) missense probably benign 0.00
R9433:Vmn2r67 UTSW 7 84,804,917 (GRCm39) missense possibly damaging 0.60
R9453:Vmn2r67 UTSW 7 84,800,697 (GRCm39) missense probably benign 0.32
R9471:Vmn2r67 UTSW 7 84,799,723 (GRCm39) critical splice donor site probably null
R9526:Vmn2r67 UTSW 7 84,785,834 (GRCm39) missense probably benign 0.10
R9538:Vmn2r67 UTSW 7 84,801,327 (GRCm39) missense
R9544:Vmn2r67 UTSW 7 84,786,317 (GRCm39) missense possibly damaging 0.53
R9574:Vmn2r67 UTSW 7 84,786,017 (GRCm39) missense probably benign 0.00
R9599:Vmn2r67 UTSW 7 84,804,941 (GRCm39) missense probably damaging 0.96
R9768:Vmn2r67 UTSW 7 84,802,037 (GRCm39) missense probably benign 0.23
Posted On 2013-10-07