Incidental Mutation 'R7086:Vmn2r87'
ID 549904
Institutional Source Beutler Lab
Gene Symbol Vmn2r87
Ensembl Gene ENSMUSG00000091511
Gene Name vomeronasal 2, receptor 87
Synonyms EG625131
MMRRC Submission 045180-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R7086 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 130307690-130333248 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 130333178 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 24 (T24K)
Ref Sequence ENSEMBL: ENSMUSP00000129215 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164227]
AlphaFold E9PZX4
Predicted Effect probably benign
Transcript: ENSMUST00000164227
AA Change: T24K

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000129215
Gene: ENSMUSG00000091511
AA Change: T24K

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 77 422 1.8e-27 PFAM
Pfam:NCD3G 508 562 1.8e-19 PFAM
Pfam:7tm_3 595 829 8.8e-55 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 98% (60/61)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam30 A G 3: 98,068,635 (GRCm39) H28R probably damaging Het
Adgre4 T C 17: 56,127,649 (GRCm39) I563T probably benign Het
Ankub1 A T 3: 57,597,746 (GRCm39) C75S probably damaging Het
Antxrl G A 14: 33,787,873 (GRCm39) V299I probably benign Het
Arfgef2 T A 2: 166,718,536 (GRCm39) C1442S probably damaging Het
Atp13a3 T C 16: 30,169,881 (GRCm39) D399G possibly damaging Het
Cacna2d1 T A 5: 16,554,414 (GRCm39) Y666N probably damaging Het
Cenpo C T 12: 4,265,307 (GRCm39) E238K probably benign Het
Cfap91 A T 16: 38,127,219 (GRCm39) F512L possibly damaging Het
Chrng C A 1: 87,138,735 (GRCm39) R455S probably benign Het
Cimap1a A G 7: 140,429,402 (GRCm39) H151R probably benign Het
Cluh T A 11: 74,558,166 (GRCm39) H1155Q possibly damaging Het
Col16a1 G A 4: 129,946,773 (GRCm39) probably null Het
Cpne5 G A 17: 29,378,051 (GRCm39) P576L unknown Het
Crocc C A 4: 140,774,368 (GRCm39) V144L possibly damaging Het
Cubn A G 2: 13,324,669 (GRCm39) V2781A probably damaging Het
Cyp8b1 A G 9: 121,744,355 (GRCm39) F326L probably benign Het
Dclk1 G A 3: 55,395,333 (GRCm39) probably null Het
Dennd2b A G 7: 109,124,781 (GRCm39) I1083T probably damaging Het
Dnah7c A G 1: 46,789,285 (GRCm39) R3303G probably benign Het
Dnhd1 G T 7: 105,357,739 (GRCm39) R3191S probably benign Het
Fgfbp3 T G 19: 36,896,103 (GRCm39) S172R possibly damaging Het
Gpr158 G A 2: 21,831,386 (GRCm39) V829I probably benign Het
Gtse1 A G 15: 85,759,750 (GRCm39) D647G probably damaging Het
H2-Q7 T A 17: 35,658,461 (GRCm39) V33E probably damaging Het
Hydin A G 8: 111,326,877 (GRCm39) T4739A possibly damaging Het
Kcnip1 G T 11: 33,584,629 (GRCm39) P175T probably damaging Het
Klhl10 T C 11: 100,347,768 (GRCm39) V608A probably benign Het
Klhl2 A G 8: 65,275,664 (GRCm39) Y80H probably damaging Het
Lnx2 A T 5: 146,956,988 (GRCm39) probably null Het
Lst1 G A 17: 35,404,262 (GRCm39) H59Y probably damaging Het
Mphosph8 G C 14: 56,905,980 (GRCm39) V58L possibly damaging Het
Mpnd C A 17: 56,316,457 (GRCm39) S45R possibly damaging Het
Myh8 A G 11: 67,183,453 (GRCm39) probably null Het
Or12j4 A G 7: 140,046,341 (GRCm39) T76A possibly damaging Het
Or4c52 A G 2: 89,845,594 (GRCm39) I107V probably benign Het
Phox2a A G 7: 101,467,718 (GRCm39) Y5C probably damaging Het
Pkdrej A G 15: 85,704,317 (GRCm39) S540P probably damaging Het
Plcb4 A G 2: 135,849,767 (GRCm39) M1133V probably benign Het
Plxnc1 T C 10: 94,667,297 (GRCm39) M1126V probably benign Het
Ppm1l A G 3: 69,225,186 (GRCm39) Y96C probably damaging Het
Prpsap1 T C 11: 116,368,109 (GRCm39) T234A probably benign Het
R3hcc1l T C 19: 42,570,409 (GRCm39) V668A probably damaging Het
Rapgef2 A G 3: 78,993,353 (GRCm39) S712P probably benign Het
Rcc2 T C 4: 140,435,280 (GRCm39) C100R probably benign Het
Recql4 C A 15: 76,589,753 (GRCm39) G764V unknown Het
Rlbp1 A G 7: 79,029,813 (GRCm39) I140T possibly damaging Het
Samsn1 T C 16: 75,667,794 (GRCm39) T261A probably benign Het
Sgtb T C 13: 104,254,924 (GRCm39) S65P possibly damaging Het
Spag9 T C 11: 93,988,690 (GRCm39) V920A probably benign Het
Spata31 T A 13: 65,070,043 (GRCm39) S730R probably benign Het
Spta1 C T 1: 174,027,050 (GRCm39) A841V probably damaging Het
Tnfaip1 T C 11: 78,416,265 (GRCm39) S273G probably benign Het
Vezf1 T C 11: 87,969,364 (GRCm39) V371A probably benign Het
Vmn1r67 G A 7: 10,181,044 (GRCm39) V103I possibly damaging Het
Wdr43 G A 17: 71,923,434 (GRCm39) G60D probably benign Het
Xkr4 G A 1: 3,287,185 (GRCm39) T335I probably damaging Het
Zdhhc23 A T 16: 43,791,873 (GRCm39) I300N probably damaging Het
Zfp729b T C 13: 67,741,056 (GRCm39) K403R probably damaging Het
Other mutations in Vmn2r87
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01090:Vmn2r87 APN 10 130,333,247 (GRCm39) start codon destroyed probably null 1.00
IGL01295:Vmn2r87 APN 10 130,307,878 (GRCm39) missense probably damaging 1.00
IGL01411:Vmn2r87 APN 10 130,308,429 (GRCm39) missense probably benign 0.03
IGL01680:Vmn2r87 APN 10 130,315,586 (GRCm39) nonsense probably null
IGL01822:Vmn2r87 APN 10 130,307,991 (GRCm39) missense probably damaging 1.00
IGL01835:Vmn2r87 APN 10 130,314,978 (GRCm39) missense probably damaging 1.00
IGL01965:Vmn2r87 APN 10 130,314,924 (GRCm39) missense possibly damaging 0.49
IGL02562:Vmn2r87 APN 10 130,314,513 (GRCm39) missense probably damaging 1.00
IGL02665:Vmn2r87 APN 10 130,333,049 (GRCm39) missense probably benign 0.16
IGL03202:Vmn2r87 APN 10 130,333,091 (GRCm39) missense probably benign
FR4304:Vmn2r87 UTSW 10 130,314,583 (GRCm39) missense probably benign 0.01
FR4340:Vmn2r87 UTSW 10 130,314,583 (GRCm39) missense probably benign 0.01
FR4342:Vmn2r87 UTSW 10 130,314,583 (GRCm39) missense probably benign 0.01
FR4589:Vmn2r87 UTSW 10 130,314,583 (GRCm39) missense probably benign 0.01
LCD18:Vmn2r87 UTSW 10 130,314,583 (GRCm39) missense probably benign 0.01
R0344:Vmn2r87 UTSW 10 130,315,806 (GRCm39) missense probably damaging 1.00
R0374:Vmn2r87 UTSW 10 130,307,848 (GRCm39) missense probably damaging 1.00
R0384:Vmn2r87 UTSW 10 130,307,712 (GRCm39) missense probably benign
R1144:Vmn2r87 UTSW 10 130,312,098 (GRCm39) splice site probably benign
R1172:Vmn2r87 UTSW 10 130,313,453 (GRCm39) missense probably benign 0.03
R1860:Vmn2r87 UTSW 10 130,315,755 (GRCm39) missense probably benign 0.00
R1866:Vmn2r87 UTSW 10 130,308,441 (GRCm39) missense possibly damaging 0.88
R1897:Vmn2r87 UTSW 10 130,307,829 (GRCm39) missense probably damaging 1.00
R2360:Vmn2r87 UTSW 10 130,315,631 (GRCm39) missense probably damaging 0.99
R2909:Vmn2r87 UTSW 10 130,314,865 (GRCm39) missense probably damaging 0.99
R3874:Vmn2r87 UTSW 10 130,315,856 (GRCm39) missense possibly damaging 0.62
R4113:Vmn2r87 UTSW 10 130,315,691 (GRCm39) missense probably benign
R4190:Vmn2r87 UTSW 10 130,308,556 (GRCm39) missense probably damaging 1.00
R4197:Vmn2r87 UTSW 10 130,315,779 (GRCm39) missense possibly damaging 0.55
R4201:Vmn2r87 UTSW 10 130,308,448 (GRCm39) missense probably benign 0.03
R4202:Vmn2r87 UTSW 10 130,308,448 (GRCm39) missense probably benign 0.03
R4368:Vmn2r87 UTSW 10 130,315,676 (GRCm39) missense probably benign 0.44
R4485:Vmn2r87 UTSW 10 130,315,678 (GRCm39) nonsense probably null
R4537:Vmn2r87 UTSW 10 130,308,054 (GRCm39) missense probably benign 0.12
R4590:Vmn2r87 UTSW 10 130,315,014 (GRCm39) missense possibly damaging 0.69
R4752:Vmn2r87 UTSW 10 130,314,336 (GRCm39) nonsense probably null
R4873:Vmn2r87 UTSW 10 130,308,367 (GRCm39) missense probably damaging 1.00
R4875:Vmn2r87 UTSW 10 130,308,367 (GRCm39) missense probably damaging 1.00
R4923:Vmn2r87 UTSW 10 130,314,435 (GRCm39) missense probably damaging 0.99
R4970:Vmn2r87 UTSW 10 130,314,422 (GRCm39) missense probably damaging 1.00
R5049:Vmn2r87 UTSW 10 130,308,298 (GRCm39) missense probably damaging 0.96
R5112:Vmn2r87 UTSW 10 130,314,422 (GRCm39) missense probably damaging 1.00
R5187:Vmn2r87 UTSW 10 130,333,208 (GRCm39) missense probably null 0.99
R5618:Vmn2r87 UTSW 10 130,315,817 (GRCm39) missense probably damaging 1.00
R6057:Vmn2r87 UTSW 10 130,308,226 (GRCm39) missense probably benign 0.02
R6220:Vmn2r87 UTSW 10 130,315,807 (GRCm39) missense probably benign 0.01
R6287:Vmn2r87 UTSW 10 130,314,291 (GRCm39) critical splice donor site probably null
R6383:Vmn2r87 UTSW 10 130,314,869 (GRCm39) missense probably damaging 1.00
R6576:Vmn2r87 UTSW 10 130,314,654 (GRCm39) missense probably benign 0.05
R6742:Vmn2r87 UTSW 10 130,308,396 (GRCm39) missense probably damaging 1.00
R7162:Vmn2r87 UTSW 10 130,313,416 (GRCm39) missense probably benign 0.08
R7419:Vmn2r87 UTSW 10 130,307,992 (GRCm39) missense probably damaging 1.00
R7425:Vmn2r87 UTSW 10 130,314,761 (GRCm39) missense probably damaging 1.00
R7443:Vmn2r87 UTSW 10 130,308,588 (GRCm39) missense probably damaging 1.00
R7571:Vmn2r87 UTSW 10 130,314,940 (GRCm39) missense probably damaging 0.99
R7663:Vmn2r87 UTSW 10 130,308,054 (GRCm39) missense probably damaging 0.97
R7716:Vmn2r87 UTSW 10 130,308,018 (GRCm39) missense probably benign 0.09
R7793:Vmn2r87 UTSW 10 130,313,413 (GRCm39) missense probably benign 0.05
R7806:Vmn2r87 UTSW 10 130,315,679 (GRCm39) missense probably benign
R7841:Vmn2r87 UTSW 10 130,333,095 (GRCm39) missense probably benign 0.31
R8326:Vmn2r87 UTSW 10 130,308,180 (GRCm39) missense possibly damaging 0.67
R8411:Vmn2r87 UTSW 10 130,308,126 (GRCm39) missense probably damaging 0.99
R8445:Vmn2r87 UTSW 10 130,313,335 (GRCm39) missense probably damaging 1.00
R8540:Vmn2r87 UTSW 10 130,314,762 (GRCm39) missense possibly damaging 0.74
R8892:Vmn2r87 UTSW 10 130,308,105 (GRCm39) missense probably damaging 0.99
R9093:Vmn2r87 UTSW 10 130,308,165 (GRCm39) missense probably benign 0.08
R9623:Vmn2r87 UTSW 10 130,315,794 (GRCm39) missense probably damaging 1.00
R9667:Vmn2r87 UTSW 10 130,314,776 (GRCm39) missense probably damaging 1.00
R9797:Vmn2r87 UTSW 10 130,312,064 (GRCm39) missense probably benign 0.44
R9797:Vmn2r87 UTSW 10 130,308,138 (GRCm39) missense probably damaging 0.99
Z1088:Vmn2r87 UTSW 10 130,308,183 (GRCm39) missense probably damaging 0.98
Z1176:Vmn2r87 UTSW 10 130,307,713 (GRCm39) missense probably benign 0.04
Predicted Primers PCR Primer
(F):5'- AGAATCCACAGTTTGTGTACACAG -3'
(R):5'- TGTCCAGGGAGCATGACATAG -3'

Sequencing Primer
(F):5'- CCATAGGTTTCTCCATTGTC -3'
(R):5'- AAGTGGTAATTATATTCAGACAGCAG -3'
Posted On 2019-05-15