Incidental Mutation 'R2023:Vmn2r101'
ID 220196
Institutional Source Beutler Lab
Gene Symbol Vmn2r101
Ensembl Gene ENSMUSG00000094892
Gene Name vomeronasal 2, receptor 101
Synonyms EG627576
MMRRC Submission 040032-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.124) question?
Stock # R2023 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 19797493-19832579 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 19810368 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 385 (R385*)
Ref Sequence ENSEMBL: ENSMUSP00000131583 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171914]
AlphaFold E9PZS9
Predicted Effect probably null
Transcript: ENSMUST00000171914
AA Change: R385*
SMART Domains Protein: ENSMUSP00000131583
Gene: ENSMUSG00000094892
AA Change: R385*

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 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 92.4%
Validation Efficiency 97% (60/62)
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik1 A G 11: 48,839,247 (GRCm39) S447P possibly damaging Het
9930111J21Rik2 A G 11: 48,911,144 (GRCm39) F430L probably benign Het
Acap2 A G 16: 30,938,233 (GRCm39) V297A probably damaging Het
Adam3 G A 8: 25,179,479 (GRCm39) R613C possibly damaging Het
Akt1 C T 12: 112,626,071 (GRCm39) R67Q probably benign Het
Ambp T C 4: 63,069,702 (GRCm39) Y108C probably damaging Het
Apob A G 12: 8,061,090 (GRCm39) I3158V probably benign Het
Bank1 T C 3: 136,031,679 (GRCm39) T8A probably benign Het
Casp8ap2 T C 4: 32,644,560 (GRCm39) V1211A probably benign Het
Ccdc88a G T 11: 29,413,546 (GRCm39) E695* probably null Het
Cep68 A C 11: 20,189,888 (GRCm39) S375A probably benign Het
Cfap44 A G 16: 44,236,375 (GRCm39) I417V probably benign Het
Chrna2 T A 14: 66,379,677 (GRCm39) H5Q probably benign Het
Cog7 A T 7: 121,536,193 (GRCm39) I549K probably damaging Het
Col28a1 C A 6: 8,083,783 (GRCm39) S558I possibly damaging Het
Cyp4f14 A G 17: 33,125,505 (GRCm39) I385T probably damaging Het
Dynlt4 A G 4: 116,985,504 (GRCm39) E109G possibly damaging Het
Erap1 T A 13: 74,814,627 (GRCm39) V451E probably benign Het
Frem1 G T 4: 82,831,795 (GRCm39) T1988K probably benign Het
Gm10277 TC T 11: 77,676,828 (GRCm39) probably null Het
Gm5616 A G 9: 48,361,928 (GRCm39) noncoding transcript Het
Gm5709 T C 3: 59,543,142 (GRCm39) noncoding transcript Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Hsd11b1 T C 1: 192,922,686 (GRCm39) T124A probably benign Het
Itpr3 T A 17: 27,321,785 (GRCm39) M1054K possibly damaging Het
Kars1 T C 8: 112,728,484 (GRCm39) N200S probably benign Het
Kdm2a C A 19: 4,372,492 (GRCm39) R951L probably damaging Het
Ldhd T A 8: 112,356,578 (GRCm39) H61L probably damaging Het
Macf1 G T 4: 123,366,523 (GRCm39) A2746E probably damaging Het
Micall2 A G 5: 139,703,266 (GRCm39) V190A possibly damaging Het
Mis18bp1 A T 12: 65,195,883 (GRCm39) V627E probably damaging Het
Muc4 A T 16: 32,574,054 (GRCm39) T711S probably benign Het
Notch4 T C 17: 34,806,502 (GRCm39) L1813P probably damaging Het
Nox3 A G 17: 3,744,296 (GRCm39) probably benign Het
Or4b1d G T 2: 89,969,200 (GRCm39) C94* probably null Het
Or5p63 A G 7: 107,811,049 (GRCm39) L229P probably damaging Het
Or6c1b T A 10: 129,273,451 (GRCm39) Y257N probably damaging Het
Osbpl2 C A 2: 179,791,969 (GRCm39) probably null Het
Pamr1 T A 2: 102,464,880 (GRCm39) M343K probably benign Het
Pcdh15 T G 10: 74,467,025 (GRCm39) S1684A possibly damaging Het
Pgr T A 9: 8,958,399 (GRCm39) V802D probably damaging Het
Pgs1 A G 11: 117,893,228 (GRCm39) E55G probably benign Het
Pkd2 T A 5: 104,614,744 (GRCm39) probably null Het
Ppp3r2 T C 4: 49,681,723 (GRCm39) I76V probably benign Het
Ptprd C T 4: 75,875,341 (GRCm39) E1240K probably damaging Het
Recql5 G A 11: 115,784,466 (GRCm39) T878I probably benign Het
Rnf17 A G 14: 56,669,036 (GRCm39) D233G possibly damaging Het
Sectm1a A G 11: 120,960,408 (GRCm39) probably benign Het
Smo A G 6: 29,754,715 (GRCm39) N262D possibly damaging Het
Srcin1 A G 11: 97,416,872 (GRCm39) S931P probably benign Het
Tcof1 C T 18: 60,966,605 (GRCm39) G329R probably damaging Het
Thsd7a G A 6: 12,327,535 (GRCm39) H1446Y probably benign Het
Tlr11 A G 14: 50,600,026 (GRCm39) T671A probably damaging Het
Tmem171 C A 13: 98,828,733 (GRCm39) W139L probably damaging Het
Vps13c A T 9: 67,843,567 (GRCm39) probably benign Het
Wdr87-ps G T 7: 29,230,959 (GRCm39) noncoding transcript Het
Zfp287 A C 11: 62,605,808 (GRCm39) Y366* probably null Het
Zfp456 A T 13: 67,514,616 (GRCm39) C363* probably null Het
Zfp523 A G 17: 28,419,978 (GRCm39) probably benign Het
Zfp667 A C 7: 6,308,416 (GRCm39) K361N possibly damaging 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
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
R7375:Vmn2r101 UTSW 17 19,831,652 (GRCm39) missense probably damaging 1.00
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'- AGACTCATTCCATGGAAGCC -3'
(R):5'- TGCAAATCTCTTATGCCAGAGTG -3'

Sequencing Primer
(F):5'- CCATGGAAGCCTAATTTTTAAGCAC -3'
(R):5'- TCTCTTATGCCAGAGTGATGAC -3'
Posted On 2014-08-25