Incidental Mutation 'R7375:Vmn2r101'
ID 572354
Institutional Source Beutler Lab
Gene Symbol Vmn2r101
Ensembl Gene ENSMUSG00000094892
Gene Name vomeronasal 2, receptor 101
Synonyms EG627576
MMRRC Submission 045458-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.124) question?
Stock # R7375 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 19797493-19832579 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 19831652 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 549 (D549E)
Ref Sequence ENSEMBL: ENSMUSP00000131583 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171914]
AlphaFold E9PZS9
Predicted Effect probably damaging
Transcript: ENSMUST00000171914
AA Change: D549E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000131583
Gene: ENSMUSG00000094892
AA Change: D549E

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 82 466 1.6e-36 PFAM
Pfam:NCD3G 509 562 6.4e-22 PFAM
Pfam:7tm_3 595 830 1.4e-51 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A G 5: 8,968,671 (GRCm39) I337V probably benign Het
Abl2 A G 1: 156,450,184 (GRCm39) D117G probably damaging Het
Arhgap5 T A 12: 52,563,365 (GRCm39) L112* probably null Het
Brinp3 C G 1: 146,777,748 (GRCm39) L732V possibly damaging Het
Ccdc168 A T 1: 44,099,694 (GRCm39) I468N possibly damaging Het
Cfap91 T A 16: 38,155,980 (GRCm39) H81L probably damaging Het
Cmya5 T G 13: 93,228,169 (GRCm39) K2306N probably damaging Het
Col16a1 A C 4: 129,959,294 (GRCm39) K680T unknown Het
Col28a1 T A 6: 7,998,499 (GRCm39) T1137S possibly damaging Het
Crnn A T 3: 93,056,452 (GRCm39) T413S possibly damaging Het
Csf1 A G 3: 107,655,495 (GRCm39) L512P possibly damaging Het
Dlx3 C A 11: 95,011,461 (GRCm39) A105D possibly damaging Het
Dnah3 T G 7: 119,550,900 (GRCm39) T161P probably damaging Het
Dnah7b A G 1: 46,342,794 (GRCm39) D3435G probably damaging Het
Dpp10 A G 1: 123,295,524 (GRCm39) I541T probably benign Het
Efcc1 T C 6: 87,728,838 (GRCm39) V431A possibly damaging Het
Enpp5 T C 17: 44,391,868 (GRCm39) I99T probably benign Het
Gm11232 C T 4: 71,675,583 (GRCm39) W59* probably null Het
Gxylt2 A T 6: 100,727,383 (GRCm39) T166S probably benign Het
Herc6 A T 6: 57,628,791 (GRCm39) probably null Het
Itga2 T C 13: 115,005,753 (GRCm39) I476V probably benign Het
Kcnq5 T C 1: 21,539,710 (GRCm39) T403A possibly damaging Het
Klhl42 A G 6: 146,993,538 (GRCm39) K170R probably benign Het
Klk13 T C 7: 43,370,582 (GRCm39) probably null Het
Krt32 G T 11: 99,972,050 (GRCm39) R433S probably benign Het
Lrp1 G T 10: 127,375,217 (GRCm39) T4461N probably damaging Het
Mapk10 A T 5: 103,124,256 (GRCm39) M256K probably null Het
Mogat2 T C 7: 98,872,905 (GRCm39) K93R probably damaging Het
Myh1 G T 11: 67,101,254 (GRCm39) V677L probably damaging Het
Naip5 G T 13: 100,356,205 (GRCm39) Q1137K not run Het
Naip5 T C 13: 100,356,204 (GRCm39) Q1137R probably benign Het
Oog4 G A 4: 143,165,544 (GRCm39) T201M possibly damaging Het
Or4a70 C T 2: 89,324,036 (GRCm39) G207R possibly damaging Het
Pik3c2a T C 7: 115,975,621 (GRCm39) T649A probably damaging Het
Plec T A 15: 76,061,555 (GRCm39) H2794L possibly damaging Het
Pros1 T A 16: 62,744,913 (GRCm39) N509K probably damaging Het
Psme3ip1 G A 8: 95,309,636 (GRCm39) L119F probably benign Het
Psme4 T A 11: 30,722,700 (GRCm39) probably null Het
Ptprf A G 4: 118,070,011 (GRCm39) V1457A probably benign Het
Rad50 A G 11: 53,543,055 (GRCm39) probably null Het
Rfx5 C T 3: 94,866,053 (GRCm39) P451S unknown Het
Scpppq1 G T 5: 104,219,123 (GRCm39) probably null Het
Sdk1 G T 5: 141,984,598 (GRCm39) V728L probably benign Het
Sfxn4 T C 19: 60,847,112 (GRCm39) D57G probably benign Het
Slc10a4 A G 5: 73,169,650 (GRCm39) D425G probably benign Het
Slc17a5 C T 9: 78,495,174 (GRCm39) A26T probably benign Het
Slc22a26 A T 19: 7,760,509 (GRCm39) probably null Het
Slc22a30 A G 19: 8,382,055 (GRCm39) L72P probably damaging Het
Slco6c1 T C 1: 97,009,146 (GRCm39) T447A possibly damaging Het
Slco6d1 A G 1: 98,349,172 (GRCm39) N81S probably damaging Het
Stard9 T C 2: 120,495,483 (GRCm39) probably null Het
Tecpr1 T C 5: 144,145,417 (GRCm39) E610G possibly damaging Het
Tmem81 G T 1: 132,435,301 (GRCm39) V36L possibly damaging Het
Trabd2b G T 4: 114,467,194 (GRCm39) K474N probably benign Het
Tspan33 T C 6: 29,713,519 (GRCm39) F149L probably benign Het
Ttn A G 2: 76,606,683 (GRCm39) Y18076H probably damaging Het
Utrn G A 10: 12,516,764 (GRCm39) R2277C probably damaging Het
Vmn2r107 T A 17: 20,576,138 (GRCm39) I156K probably benign Het
Wwc2 T G 8: 48,316,955 (GRCm39) S713R unknown Het
Xndc1 C A 7: 101,730,687 (GRCm39) probably null Het
Zfp810 A G 9: 22,201,833 (GRCm39) probably null Het
Other mutations in Vmn2r101
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01121:Vmn2r101 APN 17 19,809,936 (GRCm39) missense probably damaging 0.99
IGL02125:Vmn2r101 APN 17 19,809,963 (GRCm39) missense possibly damaging 0.95
IGL02300:Vmn2r101 APN 17 19,832,199 (GRCm39) missense probably damaging 1.00
IGL02682:Vmn2r101 APN 17 19,832,507 (GRCm39) missense possibly damaging 0.82
IGL02825:Vmn2r101 APN 17 19,810,132 (GRCm39) missense probably benign 0.00
IGL02862:Vmn2r101 APN 17 19,831,867 (GRCm39) missense probably damaging 1.00
IGL02943:Vmn2r101 APN 17 19,831,666 (GRCm39) missense probably damaging 0.99
R0371:Vmn2r101 UTSW 17 19,810,394 (GRCm39) missense probably benign 0.07
R0462:Vmn2r101 UTSW 17 19,810,431 (GRCm39) missense probably benign 0.04
R0492:Vmn2r101 UTSW 17 19,809,245 (GRCm39) missense probably damaging 1.00
R0654:Vmn2r101 UTSW 17 19,810,373 (GRCm39) missense probably benign 0.01
R1120:Vmn2r101 UTSW 17 19,797,723 (GRCm39) splice site probably benign
R1323:Vmn2r101 UTSW 17 19,832,313 (GRCm39) missense probably damaging 1.00
R1323:Vmn2r101 UTSW 17 19,832,313 (GRCm39) missense probably damaging 1.00
R1676:Vmn2r101 UTSW 17 19,832,184 (GRCm39) missense probably benign 0.00
R2023:Vmn2r101 UTSW 17 19,810,368 (GRCm39) nonsense probably null
R2149:Vmn2r101 UTSW 17 19,809,225 (GRCm39) missense probably benign 0.00
R2350:Vmn2r101 UTSW 17 19,810,045 (GRCm39) missense probably benign 0.01
R2760:Vmn2r101 UTSW 17 19,809,901 (GRCm39) missense probably benign 0.14
R3085:Vmn2r101 UTSW 17 19,809,077 (GRCm39) splice site probably null
R3086:Vmn2r101 UTSW 17 19,809,077 (GRCm39) splice site probably null
R3719:Vmn2r101 UTSW 17 19,809,811 (GRCm39) missense possibly damaging 0.50
R3771:Vmn2r101 UTSW 17 19,809,919 (GRCm39) missense probably benign
R3773:Vmn2r101 UTSW 17 19,809,919 (GRCm39) missense probably benign
R4225:Vmn2r101 UTSW 17 19,831,951 (GRCm39) missense probably damaging 1.00
R4248:Vmn2r101 UTSW 17 19,809,376 (GRCm39) missense probably damaging 1.00
R4290:Vmn2r101 UTSW 17 19,832,303 (GRCm39) missense probably damaging 1.00
R4291:Vmn2r101 UTSW 17 19,832,303 (GRCm39) missense probably damaging 1.00
R4293:Vmn2r101 UTSW 17 19,832,303 (GRCm39) missense probably damaging 1.00
R4307:Vmn2r101 UTSW 17 19,810,423 (GRCm39) missense probably damaging 1.00
R4721:Vmn2r101 UTSW 17 19,832,287 (GRCm39) missense probably damaging 0.99
R4829:Vmn2r101 UTSW 17 19,832,229 (GRCm39) missense probably benign 0.03
R5022:Vmn2r101 UTSW 17 19,831,649 (GRCm39) critical splice acceptor site probably null
R5110:Vmn2r101 UTSW 17 19,831,897 (GRCm39) missense possibly damaging 0.92
R5244:Vmn2r101 UTSW 17 19,831,788 (GRCm39) missense probably damaging 1.00
R5397:Vmn2r101 UTSW 17 19,809,104 (GRCm39) missense probably damaging 1.00
R5875:Vmn2r101 UTSW 17 19,809,092 (GRCm39) missense probably damaging 0.99
R5944:Vmn2r101 UTSW 17 19,809,769 (GRCm39) missense probably benign 0.00
R6216:Vmn2r101 UTSW 17 19,811,267 (GRCm39) missense probably benign 0.00
R6334:Vmn2r101 UTSW 17 19,810,112 (GRCm39) missense possibly damaging 0.83
R6512:Vmn2r101 UTSW 17 19,809,146 (GRCm39) missense probably damaging 1.00
R6607:Vmn2r101 UTSW 17 19,832,296 (GRCm39) missense probably damaging 1.00
R6965:Vmn2r101 UTSW 17 19,811,284 (GRCm39) missense probably benign 0.00
R7101:Vmn2r101 UTSW 17 19,809,350 (GRCm39) missense probably null 0.14
R7183:Vmn2r101 UTSW 17 19,832,440 (GRCm39) missense probably damaging 1.00
R7344:Vmn2r101 UTSW 17 19,832,059 (GRCm39) missense probably benign 0.38
R7574:Vmn2r101 UTSW 17 19,831,899 (GRCm39) missense possibly damaging 0.91
R7575:Vmn2r101 UTSW 17 19,831,654 (GRCm39) missense probably benign 0.01
R7592:Vmn2r101 UTSW 17 19,811,443 (GRCm39) splice site probably null
R7626:Vmn2r101 UTSW 17 19,832,192 (GRCm39) nonsense probably null
R7715:Vmn2r101 UTSW 17 19,832,177 (GRCm39) missense probably damaging 1.00
R7730:Vmn2r101 UTSW 17 19,831,950 (GRCm39) missense possibly damaging 0.81
R8078:Vmn2r101 UTSW 17 19,810,507 (GRCm39) missense probably benign 0.07
R8228:Vmn2r101 UTSW 17 19,811,284 (GRCm39) missense probably benign 0.00
R8283:Vmn2r101 UTSW 17 19,832,253 (GRCm39) missense probably damaging 1.00
R8712:Vmn2r101 UTSW 17 19,811,397 (GRCm39) missense probably benign 0.24
R8765:Vmn2r101 UTSW 17 19,809,245 (GRCm39) missense probably damaging 1.00
R9091:Vmn2r101 UTSW 17 19,810,244 (GRCm39) missense probably benign
R9092:Vmn2r101 UTSW 17 19,809,807 (GRCm39) missense probably benign 0.07
R9113:Vmn2r101 UTSW 17 19,811,288 (GRCm39) missense possibly damaging 0.56
R9158:Vmn2r101 UTSW 17 19,809,161 (GRCm39) missense probably benign 0.00
R9168:Vmn2r101 UTSW 17 19,809,138 (GRCm39) missense probably damaging 1.00
R9235:Vmn2r101 UTSW 17 19,810,238 (GRCm39) missense probably damaging 0.99
R9270:Vmn2r101 UTSW 17 19,810,244 (GRCm39) missense probably benign
R9290:Vmn2r101 UTSW 17 19,811,395 (GRCm39) missense probably benign 0.05
R9296:Vmn2r101 UTSW 17 19,810,047 (GRCm39) missense probably damaging 0.98
R9602:Vmn2r101 UTSW 17 19,831,780 (GRCm39) nonsense probably null
R9706:Vmn2r101 UTSW 17 19,809,925 (GRCm39) missense probably damaging 1.00
Z1088:Vmn2r101 UTSW 17 19,809,237 (GRCm39) missense possibly damaging 0.78
Predicted Primers PCR Primer
(F):5'- GGCTCTACTGAATGAACAAAGTGG -3'
(R):5'- TCTGTGTTTCACAAAGATGCC -3'

Sequencing Primer
(F):5'- GGAAGCAACAAAGTTCACTTTATCAG -3'
(R):5'- CTGTGTTTCACAAAGATGCCAATAAC -3'
Posted On 2019-09-13