Incidental Mutation 'IGL02048:Vmn2r11'
ID 184993
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r11
Ensembl Gene ENSMUSG00000091450
Gene Name vomeronasal 2, receptor 11
Synonyms EG384219
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL02048
Quality Score
Status
Chromosome 5
Chromosomal Location 109194739-109207318 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 109202658 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 140 (I140V)
Ref Sequence ENSEMBL: ENSMUSP00000133218 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164875]
AlphaFold E9Q4X4
Predicted Effect probably benign
Transcript: ENSMUST00000164875
AA Change: I140V

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000133218
Gene: ENSMUSG00000091450
AA Change: I140V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 167 475 1.6e-29 PFAM
Pfam:NCD3G 520 574 9.1e-19 PFAM
Pfam:7tm_3 607 842 4.6e-55 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca1 C T 4: 53,069,831 (GRCm39) D1288N probably damaging Het
Abcc1 T C 16: 14,229,383 (GRCm39) F372L probably damaging Het
Adcy2 G T 13: 69,036,186 (GRCm39) N158K possibly damaging Het
Apba1 A G 19: 23,915,000 (GRCm39) probably null Het
Arap3 T C 18: 38,130,032 (GRCm39) E43G possibly damaging Het
Bet1 A T 6: 4,082,456 (GRCm39) probably null Het
Blm A G 7: 80,152,709 (GRCm39) probably benign Het
Brinp1 T C 4: 68,681,379 (GRCm39) I384V probably benign Het
Cyp3a13 T C 5: 137,917,257 (GRCm39) probably benign Het
Dlg5 A T 14: 24,222,271 (GRCm39) I480N possibly damaging Het
Exoc3l4 A G 12: 111,394,917 (GRCm39) K538R probably benign Het
Flna G T X: 73,272,106 (GRCm39) T2008K probably benign Het
Hc T A 2: 34,886,039 (GRCm39) Q1388L probably benign Het
Ifitm1 T C 7: 140,548,205 (GRCm39) S13P probably benign Het
Il1rapl2 A G X: 137,690,398 (GRCm39) I288V probably benign Het
Il31 C T 5: 123,618,553 (GRCm39) V157M possibly damaging Het
N4bp2l1 A G 5: 150,500,103 (GRCm39) probably null Het
Nell1 T C 7: 49,869,355 (GRCm39) I210T probably damaging Het
Or52b3 T C 7: 102,204,090 (GRCm39) Y200H probably damaging Het
Or7e176 T A 9: 20,171,784 (GRCm39) I216N possibly damaging Het
Phf1 A G 17: 27,153,515 (GRCm39) probably benign Het
Phf10 G A 17: 15,165,411 (GRCm39) P482S probably benign Het
Ppp6r3 T G 19: 3,523,848 (GRCm39) M522L possibly damaging Het
Qtrt1 T C 9: 21,328,651 (GRCm39) L205P probably damaging Het
Xylt2 C T 11: 94,557,171 (GRCm39) E107K possibly damaging Het
Zfp512b A T 2: 181,231,715 (GRCm39) F155Y possibly damaging Het
Zfyve27 A G 19: 42,174,296 (GRCm39) D314G probably damaging Het
Other mutations in Vmn2r11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00925:Vmn2r11 APN 5 109,194,885 (GRCm39) missense probably benign 0.00
IGL01677:Vmn2r11 APN 5 109,201,823 (GRCm39) missense possibly damaging 0.50
IGL02559:Vmn2r11 APN 5 109,200,046 (GRCm39) missense probably damaging 0.98
IGL02879:Vmn2r11 APN 5 109,201,704 (GRCm39) missense possibly damaging 0.95
IGL03084:Vmn2r11 APN 5 109,207,209 (GRCm39) missense probably benign 0.00
IGL03163:Vmn2r11 APN 5 109,201,692 (GRCm39) missense probably benign 0.41
IGL03289:Vmn2r11 APN 5 109,196,788 (GRCm39) splice site probably benign
IGL03294:Vmn2r11 APN 5 109,201,935 (GRCm39) missense probably benign 0.22
R0233:Vmn2r11 UTSW 5 109,201,968 (GRCm39) missense probably benign 0.16
R0233:Vmn2r11 UTSW 5 109,201,968 (GRCm39) missense probably benign 0.16
R0421:Vmn2r11 UTSW 5 109,207,294 (GRCm39) missense probably benign 0.00
R0549:Vmn2r11 UTSW 5 109,199,963 (GRCm39) missense possibly damaging 0.80
R0628:Vmn2r11 UTSW 5 109,195,597 (GRCm39) missense possibly damaging 0.88
R1523:Vmn2r11 UTSW 5 109,201,707 (GRCm39) missense probably benign 0.25
R1660:Vmn2r11 UTSW 5 109,201,724 (GRCm39) missense possibly damaging 0.79
R1827:Vmn2r11 UTSW 5 109,199,938 (GRCm39) missense probably benign 0.01
R1913:Vmn2r11 UTSW 5 109,202,654 (GRCm39) missense probably benign
R2260:Vmn2r11 UTSW 5 109,201,657 (GRCm39) nonsense probably null
R2400:Vmn2r11 UTSW 5 109,199,928 (GRCm39) missense probably benign 0.03
R3933:Vmn2r11 UTSW 5 109,201,260 (GRCm39) missense probably damaging 0.97
R4091:Vmn2r11 UTSW 5 109,202,616 (GRCm39) critical splice donor site probably null
R4624:Vmn2r11 UTSW 5 109,200,101 (GRCm39) missense probably damaging 0.99
R4762:Vmn2r11 UTSW 5 109,195,436 (GRCm39) missense probably damaging 1.00
R5256:Vmn2r11 UTSW 5 109,202,658 (GRCm39) missense probably benign 0.26
R5370:Vmn2r11 UTSW 5 109,195,421 (GRCm39) missense probably damaging 1.00
R5419:Vmn2r11 UTSW 5 109,207,224 (GRCm39) missense possibly damaging 0.55
R5516:Vmn2r11 UTSW 5 109,195,032 (GRCm39) missense probably damaging 0.98
R5643:Vmn2r11 UTSW 5 109,194,869 (GRCm39) missense probably damaging 1.00
R5671:Vmn2r11 UTSW 5 109,202,772 (GRCm39) missense probably benign 0.03
R5679:Vmn2r11 UTSW 5 109,202,708 (GRCm39) missense probably benign 0.00
R5739:Vmn2r11 UTSW 5 109,207,114 (GRCm39) critical splice donor site probably null
R5746:Vmn2r11 UTSW 5 109,201,560 (GRCm39) missense probably benign 0.41
R5995:Vmn2r11 UTSW 5 109,194,921 (GRCm39) missense probably damaging 1.00
R6147:Vmn2r11 UTSW 5 109,202,700 (GRCm39) missense probably benign 0.04
R6220:Vmn2r11 UTSW 5 109,201,434 (GRCm39) missense probably benign 0.09
R6374:Vmn2r11 UTSW 5 109,201,679 (GRCm39) missense possibly damaging 0.65
R6491:Vmn2r11 UTSW 5 109,196,800 (GRCm39) missense possibly damaging 0.95
R6804:Vmn2r11 UTSW 5 109,201,350 (GRCm39) missense probably damaging 1.00
R6814:Vmn2r11 UTSW 5 109,194,976 (GRCm39) missense possibly damaging 0.81
R6872:Vmn2r11 UTSW 5 109,194,976 (GRCm39) missense possibly damaging 0.81
R7014:Vmn2r11 UTSW 5 109,201,289 (GRCm39) missense probably damaging 1.00
R7041:Vmn2r11 UTSW 5 109,202,816 (GRCm39) missense probably damaging 1.00
R7043:Vmn2r11 UTSW 5 109,200,098 (GRCm39) missense probably benign 0.00
R7050:Vmn2r11 UTSW 5 109,202,657 (GRCm39) missense probably benign 0.05
R7184:Vmn2r11 UTSW 5 109,201,281 (GRCm39) missense probably damaging 1.00
R7388:Vmn2r11 UTSW 5 109,202,742 (GRCm39) missense probably benign 0.05
R7477:Vmn2r11 UTSW 5 109,207,214 (GRCm39) missense possibly damaging 0.67
R7524:Vmn2r11 UTSW 5 109,201,848 (GRCm39) missense probably benign 0.01
R7682:Vmn2r11 UTSW 5 109,195,481 (GRCm39) missense probably benign 0.02
R7715:Vmn2r11 UTSW 5 109,195,307 (GRCm39) missense probably damaging 0.99
R7869:Vmn2r11 UTSW 5 109,199,986 (GRCm39) missense probably damaging 1.00
R8094:Vmn2r11 UTSW 5 109,201,626 (GRCm39) missense probably damaging 1.00
R8277:Vmn2r11 UTSW 5 109,202,833 (GRCm39) missense probably benign 0.00
R8506:Vmn2r11 UTSW 5 109,207,270 (GRCm39) missense probably benign 0.00
R8676:Vmn2r11 UTSW 5 109,201,626 (GRCm39) missense probably damaging 1.00
R8701:Vmn2r11 UTSW 5 109,195,556 (GRCm39) missense probably damaging 1.00
R8749:Vmn2r11 UTSW 5 109,195,319 (GRCm39) missense probably damaging 0.97
R9046:Vmn2r11 UTSW 5 109,202,850 (GRCm39) missense probably benign 0.00
R9138:Vmn2r11 UTSW 5 109,201,904 (GRCm39) missense probably damaging 1.00
R9267:Vmn2r11 UTSW 5 109,199,929 (GRCm39) missense possibly damaging 0.93
R9306:Vmn2r11 UTSW 5 109,196,831 (GRCm39) missense probably damaging 1.00
R9384:Vmn2r11 UTSW 5 109,201,266 (GRCm39) missense probably damaging 1.00
R9443:Vmn2r11 UTSW 5 109,195,159 (GRCm39) nonsense probably null
R9520:Vmn2r11 UTSW 5 109,201,455 (GRCm39) missense probably benign 0.35
R9596:Vmn2r11 UTSW 5 109,201,563 (GRCm39) missense possibly damaging 0.67
R9677:Vmn2r11 UTSW 5 109,201,332 (GRCm39) missense
Posted On 2014-05-07