Incidental Mutation 'R7434:Vmn1r103'
ID 576627
Institutional Source Beutler Lab
Gene Symbol Vmn1r103
Ensembl Gene ENSMUSG00000096663
Gene Name vomeronasal 1 receptor 103
Synonyms Gm8474
MMRRC Submission 045511-MU
Accession Numbers
Essential gene? Not available question?
Stock # R7434 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 20243542-20244459 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 20244435 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 9 (K9E)
Ref Sequence ENSEMBL: ENSMUSP00000128293 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163461]
AlphaFold K7N6X7
Predicted Effect probably damaging
Transcript: ENSMUST00000163461
AA Change: K9E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000128293
Gene: ENSMUSG00000096663
AA Change: K9E

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 3.1e-15 PFAM
Pfam:7tm_1 40 289 1.8e-8 PFAM
Pfam:V1R 41 296 1.4e-16 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (43/43)
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl1 T C 4: 86,344,115 (GRCm39) V1731A probably damaging Het
Bcat2 A G 7: 45,225,429 (GRCm39) probably null Het
Bcl6 T G 16: 23,788,798 (GRCm39) E523D possibly damaging Het
Cdcp3 C T 7: 130,881,212 (GRCm39) S1828F unknown Het
Col4a2 T A 8: 11,471,250 (GRCm39) N503K probably damaging Het
Cyb5r1 G A 1: 134,335,576 (GRCm39) C166Y probably benign Het
Cyp2w1 T C 5: 139,342,775 (GRCm39) V490A possibly damaging Het
Erich6b A G 14: 75,901,024 (GRCm39) I113V probably benign Het
Fabp12 C T 3: 10,312,738 (GRCm39) V95I probably benign Het
Gask1b T A 3: 79,848,669 (GRCm39) F472I probably damaging Het
Gpr3 T C 4: 132,938,448 (GRCm39) M75V probably benign Het
Grm5 T G 7: 87,779,682 (GRCm39) S1073A probably benign Het
Hoxc9 A G 15: 102,892,414 (GRCm39) K209R probably damaging Het
Irgm2 T G 11: 58,110,291 (GRCm39) V6G probably benign Het
Jakmip2 A G 18: 43,690,444 (GRCm39) V627A possibly damaging Het
Kansl1l C G 1: 66,801,262 (GRCm39) S568T probably damaging Het
Lims1 A G 10: 58,230,301 (GRCm39) T21A probably benign Het
Lpar2 G T 8: 70,279,165 (GRCm39) A320S probably benign Het
Lpcat4 A G 2: 112,073,400 (GRCm39) N235S probably damaging Het
Ly6g2 T C 15: 75,088,567 (GRCm39) F12L probably benign Het
Meis1 A T 11: 18,835,542 (GRCm39) S359T unknown Het
Mtor C T 4: 148,549,416 (GRCm39) T600I probably benign Het
Ncbp1 T C 4: 46,149,910 (GRCm39) S144P probably damaging Het
Ncor1 T C 11: 62,274,025 (GRCm39) E205G probably damaging Het
Nid1 T C 13: 13,643,049 (GRCm39) I329T probably benign Het
Nos3 T C 5: 24,587,633 (GRCm39) I1031T probably damaging Het
Nyap1 A G 5: 137,734,530 (GRCm39) S168P probably damaging Het
Or56a4 A G 7: 104,806,106 (GRCm39) V261A probably damaging Het
Pam T A 1: 97,903,515 (GRCm39) K73* probably null Het
Pcdhga11 T C 18: 37,891,005 (GRCm39) V671A probably benign Het
Ptpn18 G A 1: 34,512,445 (GRCm39) D417N possibly damaging Het
Ric1 A G 19: 29,552,180 (GRCm39) D317G probably damaging Het
Scn1a T C 2: 66,103,389 (GRCm39) E1957G probably benign Het
Srcap T C 7: 127,159,414 (GRCm39) S3097P unknown Het
Tas2r113 C T 6: 132,870,272 (GRCm39) T100I probably benign Het
Tnni1 A G 1: 135,735,260 (GRCm39) D57G Het
Trim29 G A 9: 43,246,428 (GRCm39) V575I probably damaging Het
Trpv3 G A 11: 73,179,087 (GRCm39) V499M probably damaging Het
Ubr1 C T 2: 120,693,161 (GRCm39) M1748I probably benign Het
Upk1a A T 7: 30,306,617 (GRCm39) M99K probably damaging Het
Usp16 T A 16: 87,276,207 (GRCm39) L515* probably null Het
Vwde A G 6: 13,187,639 (GRCm39) V616A probably benign Het
Zfp101 A T 17: 33,600,564 (GRCm39) S397R possibly damaging Het
Other mutations in Vmn1r103
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7032:Vmn1r103 UTSW 7 20,243,780 (GRCm39) missense possibly damaging 0.85
R7194:Vmn1r103 UTSW 7 20,244,438 (GRCm39) missense probably benign
R8786:Vmn1r103 UTSW 7 20,243,676 (GRCm39) missense probably benign 0.00
R9686:Vmn1r103 UTSW 7 20,244,353 (GRCm39) missense possibly damaging 0.50
Predicted Primers PCR Primer
(F):5'- TCTTGCCACCATGTGACTGAAG -3'
(R):5'- AGGCAATTTACCTGTAGTGTGATAG -3'

Sequencing Primer
(F):5'- CTTGCCACCATGTGACTGAAGAATTC -3'
(R):5'- ACCTGTAGTGTGATAGAATAGTGTC -3'
Posted On 2019-10-07