Incidental Mutation 'R2442:Vmn2r103'
ID 249841
Institutional Source Beutler Lab
Gene Symbol Vmn2r103
Ensembl Gene ENSMUSG00000091771
Gene Name vomeronasal 2, receptor 103
Synonyms EG627636
MMRRC Submission 040400-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R2442 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 19773363-19812536 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 19773531 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 57 (K57E)
Ref Sequence ENSEMBL: ENSMUSP00000126756 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172203]
AlphaFold E9PWW0
Predicted Effect probably benign
Transcript: ENSMUST00000172203
AA Change: K57E

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000126756
Gene: ENSMUSG00000091771
AA Change: K57E

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: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A G 17: 24,328,632 (GRCm38) V256A probably benign Het
Acap1 T C 11: 69,889,491 (GRCm38) N42S possibly damaging Het
Apoo-ps C A 13: 107,414,640 (GRCm38) noncoding transcript Het
Bri3 C T 5: 144,244,601 (GRCm38) T39I probably benign Het
Bsn A G 9: 108,106,920 (GRCm38) S3312P unknown Het
Camkmt C A 17: 85,090,775 (GRCm38) A17E possibly damaging Het
Cc2d2a G T 5: 43,671,305 (GRCm38) probably null Het
Ccdc122 G T 14: 77,091,958 (GRCm38) M150I possibly damaging Het
Celf4 A G 18: 25,753,459 (GRCm38) F57L probably damaging Het
Cep192 T A 18: 67,824,688 (GRCm38) F564Y possibly damaging Het
Ces1c T C 8: 93,123,212 (GRCm38) D38G probably damaging Het
Cts7 C A 13: 61,355,617 (GRCm38) G178* probably null Het
Dcc A T 18: 71,456,883 (GRCm38) Y681N probably damaging Het
Dhx29 A G 13: 112,946,974 (GRCm38) E521G possibly damaging Het
Dnase2a T C 8: 84,908,993 (GRCm38) V35A probably damaging Het
Eif3l A G 15: 79,085,607 (GRCm38) M268V probably damaging Het
Foxc1 A G 13: 31,808,798 (GRCm38) M531V unknown Het
Grin2c A G 11: 115,251,134 (GRCm38) Y820H probably damaging Het
Ifit1bl1 G A 19: 34,594,889 (GRCm38) A56V probably benign Het
Iqsec1 T C 6: 90,689,883 (GRCm38) E524G possibly damaging Het
Kcnt2 A G 1: 140,376,353 (GRCm38) I154V possibly damaging Het
Kdm1b T A 13: 47,062,975 (GRCm38) Y274N probably benign Het
Kntc1 T A 5: 123,810,859 (GRCm38) L1889Q probably damaging Het
Lama1 A G 17: 67,768,317 (GRCm38) T1010A probably benign Het
Mmp11 T C 10: 75,927,245 (GRCm38) N171S probably benign Het
Myom1 A G 17: 71,110,735 (GRCm38) E1409G probably damaging Het
N4bp1 A G 8: 86,862,040 (GRCm38) I90T probably damaging Het
Olfr1263 T C 2: 90,015,341 (GRCm38) V137A probably benign Het
Plcb4 T C 2: 135,950,382 (GRCm38) S342P probably damaging Het
Plg A G 17: 12,410,960 (GRCm38) E627G probably benign Het
Rsf1 CG CGACGGCGGAG 7: 97,579,908 (GRCm38) probably benign Het
Sla2 G A 2: 156,875,942 (GRCm38) R137C probably damaging Het
Slc7a14 A G 3: 31,230,320 (GRCm38) I289T probably damaging Het
Srpr G A 9: 35,212,001 (GRCm38) G43S possibly damaging Het
Tbc1d9 T C 8: 83,166,076 (GRCm38) M1T probably null Het
Tcte2 A T 17: 13,714,077 (GRCm38) I90N possibly damaging Het
Trim30c G A 7: 104,382,274 (GRCm38) P445S probably damaging Het
Trrap A G 5: 144,817,966 (GRCm38) Q1984R probably damaging Het
Ubn2 T C 6: 38,491,005 (GRCm38) S885P probably benign Het
Unc45a A G 7: 80,339,669 (GRCm38) F17S probably damaging Het
Uts2b C T 16: 27,361,032 (GRCm38) V75I probably benign Het
Vmn2r82 A G 10: 79,385,376 (GRCm38) S524G probably damaging 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
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
R6774:Vmn2r103 UTSW 17 19,773,511 (GRCm38) missense probably benign 0.14
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'- CCATGTATAAATAGGATGTTCACCTGG -3'
(R):5'- TCTGCCTGAGTGAGGAAAATGTTC -3'

Sequencing Primer
(F):5'- CAGGCTCTTGCAAATTCC -3'
(R):5'- CCTGAGTGAGGAAAATGTTCTAAATG -3'
Posted On 2014-11-12