Incidental Mutation 'R8559:Vmn2r103'
ID 660955
Institutional Source Beutler Lab
Gene Symbol Vmn2r103
Ensembl Gene ENSMUSG00000091771
Gene Name vomeronasal 2, receptor 103
Synonyms EG627636
MMRRC Submission 068522-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R8559 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 19993625-20032798 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 20032646 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 807 (M807V)
Ref Sequence ENSEMBL: ENSMUSP00000126756 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172203]
AlphaFold E9PWW0
Predicted Effect probably benign
Transcript: ENSMUST00000172203
AA Change: M807V

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000126756
Gene: ENSMUSG00000091771
AA Change: M807V

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 82 449 1.3e-37 PFAM
Pfam:NCD3G 509 562 3.5e-22 PFAM
Pfam:7tm_3 595 830 1.1e-51 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr6 T A 10: 89,568,048 (GRCm39) H19L probably benign Het
Adamts9 A T 6: 92,784,117 (GRCm39) V1579E probably benign Het
Arhgap40 C T 2: 158,383,721 (GRCm39) R435C probably damaging Het
Atp1a4 T C 1: 172,078,897 (GRCm39) D207G probably damaging Het
Btaf1 A G 19: 36,964,273 (GRCm39) N948S probably benign Het
Calcr G A 6: 3,692,603 (GRCm39) P417L probably damaging Het
Ccn2 CCCGCCAACCGC CCCGC 10: 24,471,966 (GRCm39) probably null Het
Cep250 T A 2: 155,834,656 (GRCm39) S2194T probably damaging Het
Clcn6 C T 4: 148,111,032 (GRCm39) V102M possibly damaging Het
Cog2 T C 8: 125,269,647 (GRCm39) S396P probably benign Het
Col28a1 C A 6: 8,166,681 (GRCm39) R265L unknown Het
Cpa6 C T 1: 10,478,574 (GRCm39) W254* probably null Het
Crtc2 T A 3: 90,170,904 (GRCm39) M659K possibly damaging Het
Dnah7c A G 1: 46,764,299 (GRCm39) Y3020C probably damaging Het
Dok2 C A 14: 71,014,968 (GRCm39) H232N probably benign Het
Edem3 A G 1: 151,694,169 (GRCm39) E834G probably benign Het
Elac2 T A 11: 64,872,502 (GRCm39) probably null Het
Epx T A 11: 87,755,618 (GRCm39) I689F probably damaging Het
Exd2 G A 12: 80,522,631 (GRCm39) R30H probably benign Het
Gja1 T C 10: 56,264,304 (GRCm39) L221P probably damaging Het
Gli3 T A 13: 15,834,717 (GRCm39) L400Q probably damaging Het
Gm8439 T A 4: 120,458,008 (GRCm39) W50R unknown Het
Greb1 T A 12: 16,746,436 (GRCm39) D1278V probably damaging Het
Grin3a C A 4: 49,770,555 (GRCm39) C739F probably damaging Het
Gucy2g C A 19: 55,198,786 (GRCm39) V786F probably benign Het
Hmcn1 G A 1: 150,551,789 (GRCm39) T2605I probably benign Het
Hmgxb3 T A 18: 61,288,491 (GRCm39) T459S probably benign Het
Ift172 T C 5: 31,413,921 (GRCm39) H1469R probably damaging Het
Il1rap A G 16: 26,530,884 (GRCm39) I407V probably benign Het
Inppl1 G T 7: 101,478,834 (GRCm39) S555* probably null Het
Krt8 T C 15: 101,909,979 (GRCm39) M142V probably benign Het
Lrrk1 T A 7: 65,932,075 (GRCm39) N1049I possibly damaging Het
Megf10 G A 18: 57,373,699 (GRCm39) A166T probably damaging Het
Mei4 A T 9: 81,907,684 (GRCm39) H338L probably benign Het
Mfsd2b T C 12: 4,921,471 (GRCm39) T33A possibly damaging Het
Mgat3 A T 15: 80,096,370 (GRCm39) Y399F probably damaging Het
Mtmr4 C T 11: 87,494,950 (GRCm39) T414I probably damaging Het
Muc4 T C 16: 32,754,715 (GRCm38) S1530P unknown Het
Myl4 T C 11: 104,474,930 (GRCm39) V93A possibly damaging Het
N4bp2 T A 5: 65,982,628 (GRCm39) S1627R possibly damaging Het
Narf T G 11: 121,141,258 (GRCm39) probably null Het
Nbas A C 12: 13,402,809 (GRCm39) I788L probably benign Het
Nlrc3 A G 16: 3,783,146 (GRCm39) S104P probably benign Het
Or14j6 A T 17: 38,214,719 (GRCm39) Y94F probably benign Het
Or4a68 T A 2: 89,270,528 (GRCm39) I32F probably benign Het
Or4c11 A T 2: 88,695,527 (GRCm39) I193L probably benign Het
Or8k3 A G 2: 86,058,988 (GRCm39) V109A probably benign Het
Ppp4r4 A T 12: 103,559,420 (GRCm39) T534S probably benign Het
Prg3 A G 2: 84,819,680 (GRCm39) E58G probably benign Het
Prima1 A G 12: 103,163,512 (GRCm39) V153A possibly damaging Het
Rp1 A T 1: 4,419,784 (GRCm39) Y443N probably damaging Het
Rpgrip1 T C 14: 52,386,714 (GRCm39) S882P unknown Het
Scn1a T A 2: 66,118,077 (GRCm39) D412V probably damaging Het
Srcin1 T C 11: 97,427,975 (GRCm39) T180A probably damaging Het
Suox A G 10: 128,506,600 (GRCm39) L476P probably damaging Het
Tas2r104 T C 6: 131,662,388 (GRCm39) Y107C probably damaging Het
Tubg2 T C 11: 101,047,610 (GRCm39) V65A probably damaging Het
Ubn1 T C 16: 4,882,634 (GRCm39) V365A possibly damaging Het
Vmn2r75 T A 7: 85,815,480 (GRCm39) Y128F possibly damaging Het
Vps13b A T 15: 35,876,788 (GRCm39) I2814F probably damaging Het
Vps54 T C 11: 21,214,815 (GRCm39) Y108H probably damaging Het
Wdr6 T A 9: 108,452,593 (GRCm39) E430V probably benign Het
Zfp619 T A 7: 39,186,559 (GRCm39) V863E probably benign Het
Other mutations in Vmn2r103
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Vmn2r103 APN 17 20,013,364 (GRCm39) missense probably damaging 0.98
IGL00939:Vmn2r103 APN 17 20,015,227 (GRCm39) missense probably benign 0.00
IGL01120:Vmn2r103 APN 17 20,013,259 (GRCm39) missense probably benign 0.06
IGL01403:Vmn2r103 APN 17 20,013,229 (GRCm39) missense probably benign
IGL01404:Vmn2r103 APN 17 20,032,696 (GRCm39) missense probably damaging 1.00
IGL01713:Vmn2r103 APN 17 20,014,330 (GRCm39) missense probably damaging 1.00
IGL01802:Vmn2r103 APN 17 20,019,470 (GRCm39) missense probably benign
IGL02251:Vmn2r103 APN 17 20,014,231 (GRCm39) missense possibly damaging 0.84
IGL02466:Vmn2r103 APN 17 19,993,631 (GRCm39) missense probably benign
IGL02555:Vmn2r103 APN 17 20,031,873 (GRCm39) missense probably damaging 1.00
IGL02668:Vmn2r103 APN 17 20,014,389 (GRCm39) missense probably benign 0.03
IGL02715:Vmn2r103 APN 17 20,014,218 (GRCm39) missense probably damaging 0.97
IGL02735:Vmn2r103 APN 17 20,032,510 (GRCm39) missense probably benign 0.27
IGL03101:Vmn2r103 APN 17 19,993,782 (GRCm39) missense probably damaging 0.98
R0003:Vmn2r103 UTSW 17 20,032,241 (GRCm39) missense probably damaging 0.99
R0052:Vmn2r103 UTSW 17 20,031,903 (GRCm39) missense probably benign 0.01
R0375:Vmn2r103 UTSW 17 20,013,726 (GRCm39) missense probably benign 0.12
R0375:Vmn2r103 UTSW 17 20,013,121 (GRCm39) missense probably benign 0.06
R0755:Vmn2r103 UTSW 17 19,993,830 (GRCm39) missense probably benign 0.01
R0837:Vmn2r103 UTSW 17 20,014,189 (GRCm39) missense probably damaging 0.99
R1345:Vmn2r103 UTSW 17 20,014,509 (GRCm39) missense probably damaging 1.00
R1396:Vmn2r103 UTSW 17 20,013,230 (GRCm39) missense probably benign
R1488:Vmn2r103 UTSW 17 20,013,922 (GRCm39) missense probably damaging 0.97
R1533:Vmn2r103 UTSW 17 19,993,662 (GRCm39) missense probably benign 0.01
R1590:Vmn2r103 UTSW 17 20,014,496 (GRCm39) missense probably benign
R1928:Vmn2r103 UTSW 17 20,032,029 (GRCm39) missense possibly damaging 0.95
R1942:Vmn2r103 UTSW 17 20,032,562 (GRCm39) missense probably benign 0.02
R2071:Vmn2r103 UTSW 17 20,014,056 (GRCm39) missense probably benign
R2219:Vmn2r103 UTSW 17 20,013,909 (GRCm39) missense probably damaging 1.00
R2442:Vmn2r103 UTSW 17 19,993,793 (GRCm39) missense probably benign 0.00
R2889:Vmn2r103 UTSW 17 20,013,862 (GRCm39) missense probably damaging 1.00
R3762:Vmn2r103 UTSW 17 20,032,411 (GRCm39) missense probably damaging 0.98
R4014:Vmn2r103 UTSW 17 20,013,866 (GRCm39) missense possibly damaging 0.67
R4331:Vmn2r103 UTSW 17 20,014,495 (GRCm39) missense probably benign 0.00
R4630:Vmn2r103 UTSW 17 20,013,958 (GRCm39) missense probably benign 0.04
R4631:Vmn2r103 UTSW 17 20,013,958 (GRCm39) missense probably benign 0.04
R4632:Vmn2r103 UTSW 17 20,013,958 (GRCm39) missense probably benign 0.04
R4660:Vmn2r103 UTSW 17 20,032,077 (GRCm39) missense probably damaging 1.00
R4801:Vmn2r103 UTSW 17 20,015,338 (GRCm39) missense probably benign 0.06
R4802:Vmn2r103 UTSW 17 20,015,338 (GRCm39) missense probably benign 0.06
R4931:Vmn2r103 UTSW 17 20,032,031 (GRCm39) missense probably benign 0.01
R4995:Vmn2r103 UTSW 17 19,993,773 (GRCm39) missense probably benign 0.14
R5309:Vmn2r103 UTSW 17 20,013,296 (GRCm39) missense probably benign 0.01
R5312:Vmn2r103 UTSW 17 20,013,296 (GRCm39) missense probably benign 0.01
R5329:Vmn2r103 UTSW 17 20,032,433 (GRCm39) missense probably damaging 1.00
R5611:Vmn2r103 UTSW 17 20,013,904 (GRCm39) missense probably damaging 0.99
R5684:Vmn2r103 UTSW 17 20,013,251 (GRCm39) missense probably benign 0.02
R5715:Vmn2r103 UTSW 17 20,015,201 (GRCm39) missense probably benign 0.17
R5907:Vmn2r103 UTSW 17 20,032,715 (GRCm39) missense possibly damaging 0.67
R6029:Vmn2r103 UTSW 17 20,014,478 (GRCm39) nonsense probably null
R6114:Vmn2r103 UTSW 17 20,032,587 (GRCm39) missense probably damaging 0.99
R6285:Vmn2r103 UTSW 17 20,032,406 (GRCm39) missense probably benign
R6292:Vmn2r103 UTSW 17 20,013,866 (GRCm39) missense possibly damaging 0.67
R6334:Vmn2r103 UTSW 17 20,014,344 (GRCm39) missense probably damaging 0.97
R6501:Vmn2r103 UTSW 17 20,032,166 (GRCm39) missense probably benign 0.29
R6710:Vmn2r103 UTSW 17 20,032,239 (GRCm39) missense probably damaging 1.00
R6774:Vmn2r103 UTSW 17 19,993,773 (GRCm39) missense probably benign 0.14
R6981:Vmn2r103 UTSW 17 20,013,739 (GRCm39) missense probably benign 0.00
R7768:Vmn2r103 UTSW 17 20,032,314 (GRCm39) missense probably damaging 0.99
R7816:Vmn2r103 UTSW 17 20,014,476 (GRCm39) missense probably benign 0.06
R7885:Vmn2r103 UTSW 17 20,013,385 (GRCm39) missense probably benign 0.25
R8002:Vmn2r103 UTSW 17 20,019,511 (GRCm39) missense probably damaging 1.00
R8031:Vmn2r103 UTSW 17 20,013,759 (GRCm39) missense probably benign 0.00
R8140:Vmn2r103 UTSW 17 20,032,058 (GRCm39) missense probably damaging 1.00
R8186:Vmn2r103 UTSW 17 20,032,205 (GRCm39) missense probably damaging 1.00
R9413:Vmn2r103 UTSW 17 20,032,158 (GRCm39) missense possibly damaging 0.54
R9591:Vmn2r103 UTSW 17 20,031,921 (GRCm39) missense possibly damaging 0.70
R9652:Vmn2r103 UTSW 17 20,014,027 (GRCm39) missense probably benign 0.01
R9680:Vmn2r103 UTSW 17 20,019,525 (GRCm39) nonsense probably null
R9743:Vmn2r103 UTSW 17 20,032,475 (GRCm39) missense probably damaging 1.00
Z1088:Vmn2r103 UTSW 17 20,015,309 (GRCm39) missense probably benign 0.08
Predicted Primers PCR Primer
(F):5'- GGGATATCTCTGCTTCTTGGCC -3'
(R):5'- GAGCAGTTGAATCACCAGAGC -3'

Sequencing Primer
(F):5'- TGGCCCTTGGAAGTTACACCATG -3'
(R):5'- TTGAATCACCAGAGCAAACATGG -3'
Posted On 2021-03-08