Incidental Mutation 'R6774:Vmn2r103'
ID 532315
Institutional Source Beutler Lab
Gene Symbol Vmn2r103
Ensembl Gene ENSMUSG00000091771
Gene Name vomeronasal 2, receptor 103
Synonyms EG627636
MMRRC Submission 044890-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R6774 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 19773363-19812536 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 19773511 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 50 (H50R)
Ref Sequence ENSEMBL: ENSMUSP00000126756 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172203]
AlphaFold E9PWW0
Predicted Effect probably benign
Transcript: ENSMUST00000172203
AA Change: H50R

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000126756
Gene: ENSMUSG00000091771
AA Change: H50R

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
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.8%
Validation Efficiency 98% (53/54)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A T 9: 57,256,625 (GRCm38) I822N probably damaging Het
9930111J21Rik1 A G 11: 48,947,316 (GRCm38) S815P possibly damaging Het
A430033K04Rik A G 5: 138,646,450 (GRCm38) Y199C probably benign Het
Afap1l1 A T 18: 61,755,661 (GRCm38) V113E probably benign Het
Ahnak2 C T 12: 112,773,738 (GRCm38) C494Y possibly damaging Het
Atr A T 9: 95,927,213 (GRCm38) E1981D probably benign Het
Bmp7 A G 2: 172,872,958 (GRCm38) Y353H probably damaging Het
Capn11 C T 17: 45,657,330 (GRCm38) probably benign Het
Ccdc103 T C 11: 102,882,693 (GRCm38) F47S probably damaging Het
Cmas A G 6: 142,764,421 (GRCm38) Y130C possibly damaging Het
Cntn5 T C 9: 10,144,217 (GRCm38) Y149C probably damaging Het
Col12a1 A C 9: 79,706,337 (GRCm38) S75R possibly damaging Het
Crat G A 2: 30,413,183 (GRCm38) H31Y probably damaging Het
Dnah7a A G 1: 53,698,651 (GRCm38) V41A probably benign Het
F5 C T 1: 164,186,878 (GRCm38) R573C probably damaging Het
Gcc2 A G 10: 58,281,439 (GRCm38) N1170S possibly damaging Het
Gm29666 A T 15: 84,914,059 (GRCm38) C100* probably null Het
Gm3573 A T 14: 42,187,515 (GRCm38) Y158N possibly damaging Het
Gm5346 T A 8: 43,625,183 (GRCm38) H668L probably benign Het
Gm597 A T 1: 28,776,893 (GRCm38) I686N probably benign Het
Gtf3c1 G T 7: 125,641,621 (GRCm38) A1968E possibly damaging Het
Heg1 C A 16: 33,738,268 (GRCm38) T815K probably damaging Het
Herc1 TCCC TCC 9: 66,501,188 (GRCm38) probably null Het
Kif17 A G 4: 138,274,995 (GRCm38) Y170C probably damaging Het
Kti12 G A 4: 108,848,455 (GRCm38) G189R probably benign Het
Lrp4 G A 2: 91,511,504 (GRCm38) A1821T probably benign Het
Mamdc4 T C 2: 25,566,936 (GRCm38) I610V probably benign Het
Mmp1b T C 9: 7,387,914 (GRCm38) K27E probably benign Het
Mob4 A G 1: 55,148,429 (GRCm38) probably null Het
Myc G A 15: 61,988,279 (GRCm38) probably null Het
Myo5c A T 9: 75,289,186 (GRCm38) I1305F probably benign Het
Nprl3 A G 11: 32,237,381 (GRCm38) V292A probably damaging Het
Ntng2 T C 2: 29,197,090 (GRCm38) T373A probably damaging Het
Olfr1200 C T 2: 88,767,884 (GRCm38) V144I probably benign Het
Olfr161 T A 16: 3,592,516 (GRCm38) V40D probably damaging Het
Olfr469 T A 7: 107,823,188 (GRCm38) T94S probably benign Het
Olfr863-ps1 A T 9: 19,941,774 (GRCm38) L222H unknown Het
Pard3 T C 8: 127,410,747 (GRCm38) L859P probably damaging Het
Ppcs T C 4: 119,419,088 (GRCm38) D100G probably damaging Het
Prkdc G T 16: 15,725,461 (GRCm38) probably null Het
Pwwp2b T C 7: 139,255,987 (GRCm38) V448A probably benign Het
Rapgef4 A G 2: 72,225,775 (GRCm38) K624R probably benign Het
Synj2 C T 17: 6,038,015 (GRCm38) S1447L possibly damaging Het
Tfap2a T A 13: 40,728,754 (GRCm38) N25I probably damaging Het
Tnxb C A 17: 34,709,632 (GRCm38) Y2673* probably null Het
Trim27 T A 13: 21,192,454 (GRCm38) H457Q probably damaging Het
Trim72 T G 7: 128,010,386 (GRCm38) F453L probably damaging Het
Ubr5 A T 15: 38,015,135 (GRCm38) M877K probably damaging Het
Usp10 T C 8: 119,951,972 (GRCm38) L564P probably benign Het
Usp54 A G 14: 20,577,228 (GRCm38) V454A probably damaging Het
Uspl1 T A 5: 149,214,094 (GRCm38) D701E probably benign Het
Zfp35 G A 18: 24,002,958 (GRCm38) V120I possibly damaging Het
Zfp712 T C 13: 67,041,504 (GRCm38) T320A probably benign Het
Other mutations in Vmn2r103
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Vmn2r103 APN 17 19,793,102 (GRCm38) missense probably damaging 0.98
IGL00939:Vmn2r103 APN 17 19,794,965 (GRCm38) missense probably benign 0.00
IGL01120:Vmn2r103 APN 17 19,792,997 (GRCm38) missense probably benign 0.06
IGL01403:Vmn2r103 APN 17 19,792,967 (GRCm38) missense probably benign
IGL01404:Vmn2r103 APN 17 19,812,434 (GRCm38) missense probably damaging 1.00
IGL01713:Vmn2r103 APN 17 19,794,068 (GRCm38) missense probably damaging 1.00
IGL01802:Vmn2r103 APN 17 19,799,208 (GRCm38) missense probably benign
IGL02251:Vmn2r103 APN 17 19,793,969 (GRCm38) missense possibly damaging 0.84
IGL02466:Vmn2r103 APN 17 19,773,369 (GRCm38) missense probably benign
IGL02555:Vmn2r103 APN 17 19,811,611 (GRCm38) missense probably damaging 1.00
IGL02668:Vmn2r103 APN 17 19,794,127 (GRCm38) missense probably benign 0.03
IGL02715:Vmn2r103 APN 17 19,793,956 (GRCm38) missense probably damaging 0.97
IGL02735:Vmn2r103 APN 17 19,812,248 (GRCm38) missense probably benign 0.27
IGL03101:Vmn2r103 APN 17 19,773,520 (GRCm38) missense probably damaging 0.98
R0003:Vmn2r103 UTSW 17 19,811,979 (GRCm38) missense probably damaging 0.99
R0052:Vmn2r103 UTSW 17 19,811,641 (GRCm38) missense probably benign 0.01
R0375:Vmn2r103 UTSW 17 19,793,464 (GRCm38) missense probably benign 0.12
R0375:Vmn2r103 UTSW 17 19,792,859 (GRCm38) missense probably benign 0.06
R0755:Vmn2r103 UTSW 17 19,773,568 (GRCm38) missense probably benign 0.01
R0837:Vmn2r103 UTSW 17 19,793,927 (GRCm38) missense probably damaging 0.99
R1345:Vmn2r103 UTSW 17 19,794,247 (GRCm38) missense probably damaging 1.00
R1396:Vmn2r103 UTSW 17 19,792,968 (GRCm38) missense probably benign
R1488:Vmn2r103 UTSW 17 19,793,660 (GRCm38) missense probably damaging 0.97
R1533:Vmn2r103 UTSW 17 19,773,400 (GRCm38) missense probably benign 0.01
R1590:Vmn2r103 UTSW 17 19,794,234 (GRCm38) missense probably benign
R1928:Vmn2r103 UTSW 17 19,811,767 (GRCm38) missense possibly damaging 0.95
R1942:Vmn2r103 UTSW 17 19,812,300 (GRCm38) missense probably benign 0.02
R2071:Vmn2r103 UTSW 17 19,793,794 (GRCm38) missense probably benign
R2219:Vmn2r103 UTSW 17 19,793,647 (GRCm38) missense probably damaging 1.00
R2442:Vmn2r103 UTSW 17 19,773,531 (GRCm38) missense probably benign 0.00
R2889:Vmn2r103 UTSW 17 19,793,600 (GRCm38) missense probably damaging 1.00
R3762:Vmn2r103 UTSW 17 19,812,149 (GRCm38) missense probably damaging 0.98
R4014:Vmn2r103 UTSW 17 19,793,604 (GRCm38) missense possibly damaging 0.67
R4331:Vmn2r103 UTSW 17 19,794,233 (GRCm38) missense probably benign 0.00
R4630:Vmn2r103 UTSW 17 19,793,696 (GRCm38) missense probably benign 0.04
R4631:Vmn2r103 UTSW 17 19,793,696 (GRCm38) missense probably benign 0.04
R4632:Vmn2r103 UTSW 17 19,793,696 (GRCm38) missense probably benign 0.04
R4660:Vmn2r103 UTSW 17 19,811,815 (GRCm38) missense probably damaging 1.00
R4801:Vmn2r103 UTSW 17 19,795,076 (GRCm38) missense probably benign 0.06
R4802:Vmn2r103 UTSW 17 19,795,076 (GRCm38) missense probably benign 0.06
R4931:Vmn2r103 UTSW 17 19,811,769 (GRCm38) missense probably benign 0.01
R4995:Vmn2r103 UTSW 17 19,773,511 (GRCm38) missense probably benign 0.14
R5309:Vmn2r103 UTSW 17 19,793,034 (GRCm38) missense probably benign 0.01
R5312:Vmn2r103 UTSW 17 19,793,034 (GRCm38) missense probably benign 0.01
R5329:Vmn2r103 UTSW 17 19,812,171 (GRCm38) missense probably damaging 1.00
R5611:Vmn2r103 UTSW 17 19,793,642 (GRCm38) missense probably damaging 0.99
R5684:Vmn2r103 UTSW 17 19,792,989 (GRCm38) missense probably benign 0.02
R5715:Vmn2r103 UTSW 17 19,794,939 (GRCm38) missense probably benign 0.17
R5907:Vmn2r103 UTSW 17 19,812,453 (GRCm38) missense possibly damaging 0.67
R6029:Vmn2r103 UTSW 17 19,794,216 (GRCm38) nonsense probably null
R6114:Vmn2r103 UTSW 17 19,812,325 (GRCm38) missense probably damaging 0.99
R6285:Vmn2r103 UTSW 17 19,812,144 (GRCm38) missense probably benign
R6292:Vmn2r103 UTSW 17 19,793,604 (GRCm38) missense possibly damaging 0.67
R6334:Vmn2r103 UTSW 17 19,794,082 (GRCm38) missense probably damaging 0.97
R6501:Vmn2r103 UTSW 17 19,811,904 (GRCm38) missense probably benign 0.29
R6710:Vmn2r103 UTSW 17 19,811,977 (GRCm38) missense probably damaging 1.00
R6981:Vmn2r103 UTSW 17 19,793,477 (GRCm38) missense probably benign 0.00
R7768:Vmn2r103 UTSW 17 19,812,052 (GRCm38) missense probably damaging 0.99
R7816:Vmn2r103 UTSW 17 19,794,214 (GRCm38) missense probably benign 0.06
R7885:Vmn2r103 UTSW 17 19,793,123 (GRCm38) missense probably benign 0.25
R8002:Vmn2r103 UTSW 17 19,799,249 (GRCm38) missense probably damaging 1.00
R8031:Vmn2r103 UTSW 17 19,793,497 (GRCm38) missense probably benign 0.00
R8140:Vmn2r103 UTSW 17 19,811,796 (GRCm38) missense probably damaging 1.00
R8186:Vmn2r103 UTSW 17 19,811,943 (GRCm38) missense probably damaging 1.00
R8559:Vmn2r103 UTSW 17 19,812,384 (GRCm38) missense probably benign 0.01
R9413:Vmn2r103 UTSW 17 19,811,896 (GRCm38) missense possibly damaging 0.54
R9591:Vmn2r103 UTSW 17 19,811,659 (GRCm38) missense possibly damaging 0.70
R9652:Vmn2r103 UTSW 17 19,793,765 (GRCm38) missense probably benign 0.01
R9680:Vmn2r103 UTSW 17 19,799,263 (GRCm38) nonsense probably null
R9743:Vmn2r103 UTSW 17 19,812,213 (GRCm38) missense probably damaging 1.00
Z1088:Vmn2r103 UTSW 17 19,795,047 (GRCm38) missense probably benign 0.08
Predicted Primers PCR Primer
(F):5'- TGGCATTCTCAATCCCTTGG -3'
(R):5'- TGCCTGAGTGAGGAAAATGTTC -3'

Sequencing Primer
(F):5'- AACGATGAACCAAGCATATATGTAC -3'
(R):5'- CCTGAGTGAGGAAAATGTTCTAAATG -3'
Posted On 2018-08-29