Incidental Mutation 'IGL00742:Vmn2r5'
ID 14795
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r5
Ensembl Gene ENSMUSG00000068999
Gene Name vomeronasal 2, receptor 5
Synonyms EG667060
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # IGL00742
Quality Score
Status
Chromosome 3
Chromosomal Location 64398242-64417156 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 64398834 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 715 (I715T)
Ref Sequence ENSEMBL: ENSMUSP00000135592 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170270] [ENSMUST00000177184]
AlphaFold K7N788
Predicted Effect possibly damaging
Transcript: ENSMUST00000170270
AA Change: I628T

PolyPhen 2 Score 0.529 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000131925
Gene: ENSMUSG00000068999
AA Change: I628T

DomainStartEndE-ValueType
Pfam:ANF_receptor 1 416 9.9e-78 PFAM
Pfam:NCD3G 458 511 8.5e-18 PFAM
Pfam:7tm_3 542 779 2.3e-74 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000177184
AA Change: I715T

PolyPhen 2 Score 0.667 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000135592
Gene: ENSMUSG00000068999
AA Change: I715T

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:ANF_receptor 86 503 1.8e-80 PFAM
Pfam:NCD3G 545 598 1e-14 PFAM
Pfam:7tm_3 631 865 1.4e-45 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adck5 G T 15: 76,473,300 (GRCm39) A50S possibly damaging Het
Adgrg2 C T X: 159,271,715 (GRCm39) T778M probably damaging Het
Aimp1 G A 3: 132,377,742 (GRCm39) Q208* probably null Het
Auh T C 13: 52,992,138 (GRCm39) E210G probably damaging Het
Cdh20 T G 1: 109,993,356 (GRCm39) N270K probably benign Het
Chrna9 A G 5: 66,128,458 (GRCm39) E218G probably benign Het
Cntn5 G T 9: 9,976,302 (GRCm39) T214K probably damaging Het
Col11a1 A T 3: 113,917,964 (GRCm39) D766V unknown Het
Ddb1 A G 19: 10,588,124 (GRCm39) N203S probably benign Het
Eefsec A T 6: 88,353,261 (GRCm39) L136Q possibly damaging Het
Hdac6 T C X: 7,797,568 (GRCm39) D1019G probably benign Het
Ift88 T A 14: 57,718,843 (GRCm39) probably benign Het
Igf1r T A 7: 67,839,771 (GRCm39) C693S probably benign Het
Il18r1 T A 1: 40,520,151 (GRCm39) S181T probably benign Het
Krt35 T C 11: 99,984,785 (GRCm39) Q291R probably damaging Het
Krt81 G A 15: 101,358,159 (GRCm39) R365C probably benign Het
Lpgat1 A G 1: 191,492,321 (GRCm39) E269G probably benign Het
Lpin3 A G 2: 160,735,918 (GRCm39) D66G probably damaging Het
Map9 T C 3: 82,270,727 (GRCm39) V97A probably benign Het
Mcm3ap A G 10: 76,328,769 (GRCm39) E1129G probably damaging Het
Mmrn1 A T 6: 60,935,104 (GRCm39) H200L probably damaging Het
Mycbp2 A G 14: 103,438,788 (GRCm39) L2031S probably damaging Het
Nfatc1 C T 18: 80,741,229 (GRCm39) R243H probably benign Het
Omg T A 11: 79,394,739 (GRCm39) probably benign Het
Or51ah3 A T 7: 103,210,563 (GRCm39) Y293F probably damaging Het
Postn T A 3: 54,280,315 (GRCm39) N413K possibly damaging Het
Ppp1r3a T C 6: 14,718,608 (GRCm39) T769A probably benign Het
Pvr G A 7: 19,648,784 (GRCm39) P244S probably damaging Het
Rabl6 T C 2: 25,478,699 (GRCm39) E244G probably damaging Het
Satb2 A T 1: 56,870,700 (GRCm39) N428K possibly damaging Het
Svopl A G 6: 38,007,952 (GRCm39) probably null Het
Synpo2 G T 3: 122,907,525 (GRCm39) P597Q probably damaging Het
Tacc3 T A 5: 33,818,578 (GRCm39) H4Q possibly damaging Het
Ugt2b5 C T 5: 87,275,673 (GRCm39) G393S probably damaging Het
Other mutations in Vmn2r5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01139:Vmn2r5 APN 3 64,398,826 (GRCm39) missense probably benign 0.28
IGL03293:Vmn2r5 APN 3 64,398,747 (GRCm39) missense probably benign 0.01
PIT4581001:Vmn2r5 UTSW 3 64,411,348 (GRCm39) nonsense probably null
R0063:Vmn2r5 UTSW 3 64,411,221 (GRCm39) missense probably benign 0.01
R0142:Vmn2r5 UTSW 3 64,400,009 (GRCm39) missense probably damaging 1.00
R0193:Vmn2r5 UTSW 3 64,398,951 (GRCm39) missense possibly damaging 0.91
R0219:Vmn2r5 UTSW 3 64,411,734 (GRCm39) missense probably damaging 0.99
R0313:Vmn2r5 UTSW 3 64,411,248 (GRCm39) missense probably benign
R0620:Vmn2r5 UTSW 3 64,411,235 (GRCm39) nonsense probably null
R0726:Vmn2r5 UTSW 3 64,411,186 (GRCm39) missense probably benign 0.01
R1073:Vmn2r5 UTSW 3 64,398,726 (GRCm39) nonsense probably null
R1549:Vmn2r5 UTSW 3 64,411,421 (GRCm39) missense probably damaging 1.00
R1581:Vmn2r5 UTSW 3 64,398,640 (GRCm39) missense probably damaging 1.00
R1624:Vmn2r5 UTSW 3 64,417,116 (GRCm39) missense probably benign 0.19
R1973:Vmn2r5 UTSW 3 64,411,642 (GRCm39) missense probably damaging 1.00
R1974:Vmn2r5 UTSW 3 64,411,642 (GRCm39) missense probably damaging 1.00
R1975:Vmn2r5 UTSW 3 64,411,642 (GRCm39) missense probably damaging 1.00
R1977:Vmn2r5 UTSW 3 64,411,642 (GRCm39) missense probably damaging 1.00
R2189:Vmn2r5 UTSW 3 64,417,014 (GRCm39) missense probably benign 0.27
R2484:Vmn2r5 UTSW 3 64,411,392 (GRCm39) missense possibly damaging 0.94
R4573:Vmn2r5 UTSW 3 64,411,339 (GRCm39) missense probably damaging 0.98
R5243:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R5384:Vmn2r5 UTSW 3 64,416,931 (GRCm39) missense probably benign 0.02
R5385:Vmn2r5 UTSW 3 64,416,931 (GRCm39) missense probably benign 0.02
R5587:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R5588:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R5589:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R5590:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R5739:Vmn2r5 UTSW 3 64,411,497 (GRCm39) missense probably damaging 1.00
R6113:Vmn2r5 UTSW 3 64,398,820 (GRCm39) missense probably benign 0.03
R6739:Vmn2r5 UTSW 3 64,398,637 (GRCm39) missense probably damaging 0.97
R7106:Vmn2r5 UTSW 3 64,399,104 (GRCm39) missense probably benign 0.05
R7304:Vmn2r5 UTSW 3 64,411,671 (GRCm39) missense probably damaging 0.97
R7402:Vmn2r5 UTSW 3 64,403,176 (GRCm39) missense probably benign 0.05
R7477:Vmn2r5 UTSW 3 64,399,060 (GRCm39) missense probably damaging 1.00
R7571:Vmn2r5 UTSW 3 64,411,825 (GRCm39) missense probably damaging 1.00
R7678:Vmn2r5 UTSW 3 64,416,943 (GRCm39) missense probably benign
R7874:Vmn2r5 UTSW 3 64,398,453 (GRCm39) missense probably damaging 1.00
R8110:Vmn2r5 UTSW 3 64,398,709 (GRCm39) missense probably benign 0.00
R8223:Vmn2r5 UTSW 3 64,398,726 (GRCm39) nonsense probably null
R8767:Vmn2r5 UTSW 3 64,415,103 (GRCm39) missense possibly damaging 0.79
R8896:Vmn2r5 UTSW 3 64,411,203 (GRCm39) missense probably benign 0.00
R8948:Vmn2r5 UTSW 3 64,398,522 (GRCm39) missense probably damaging 1.00
R8950:Vmn2r5 UTSW 3 64,398,522 (GRCm39) missense probably damaging 1.00
R8962:Vmn2r5 UTSW 3 64,398,564 (GRCm39) missense probably damaging 1.00
R9012:Vmn2r5 UTSW 3 64,411,915 (GRCm39) missense probably damaging 1.00
R9109:Vmn2r5 UTSW 3 64,411,411 (GRCm39) missense possibly damaging 0.58
R9126:Vmn2r5 UTSW 3 64,399,159 (GRCm39) missense probably benign 0.13
R9192:Vmn2r5 UTSW 3 64,398,938 (GRCm39) nonsense probably null
R9221:Vmn2r5 UTSW 3 64,411,721 (GRCm39) nonsense probably null
R9375:Vmn2r5 UTSW 3 64,411,316 (GRCm39) missense probably damaging 1.00
R9529:Vmn2r5 UTSW 3 64,400,018 (GRCm39) missense probably benign 0.06
Z1088:Vmn2r5 UTSW 3 64,416,963 (GRCm39) missense probably benign 0.02
Z1177:Vmn2r5 UTSW 3 64,398,472 (GRCm39) missense probably damaging 1.00
Posted On 2012-12-06