Incidental Mutation 'R3952:Vmn1r118'
ID 307995
Institutional Source Beutler Lab
Gene Symbol Vmn1r118
Ensembl Gene ENSMUSG00000094589
Gene Name vomeronasal 1 receptor 118
Synonyms Gm8542
MMRRC Submission 040829-MU
Accession Numbers
Essential gene? Not available question?
Stock # R3952 (G1)
Quality Score 114
Status Not validated
Chromosome 7
Chromosomal Location 20645352-20646272 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 20645933 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 114 (Q114K)
Ref Sequence ENSEMBL: ENSMUSP00000125956 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172322]
AlphaFold L7N273
Predicted Effect probably damaging
Transcript: ENSMUST00000172322
AA Change: Q114K

PolyPhen 2 Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000125956
Gene: ENSMUSG00000094589
AA Change: Q114K

DomainStartEndE-ValueType
Pfam:TAS2R 8 298 6.8e-18 PFAM
Pfam:7tm_1 31 288 3.2e-6 PFAM
Pfam:V1R 41 297 4.5e-16 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency 98% (46/47)
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik T C 10: 100,451,158 (GRCm39) probably benign Het
4932414N04Rik T C 2: 68,494,747 (GRCm39) probably null Het
Abi3bp C T 16: 56,424,401 (GRCm39) T450I possibly damaging Het
Abl1 A T 2: 31,674,549 (GRCm39) T213S probably damaging Het
Apc2 C T 10: 80,150,318 (GRCm39) R1762W probably damaging Het
Arl2 G T 19: 6,184,707 (GRCm39) T182N probably benign Het
Brd8 C G 18: 34,747,497 (GRCm39) probably benign Het
Cdh23 T C 10: 60,493,105 (GRCm39) Y3C probably benign Het
Clca3a2 A G 3: 144,508,822 (GRCm39) Y666H probably damaging Het
Cmya5 A G 13: 93,225,707 (GRCm39) V3127A possibly damaging Het
Copg1 G A 6: 87,882,198 (GRCm39) A598T probably benign Het
Dera A G 6: 137,814,118 (GRCm39) Y100C probably damaging Het
Epha1 C A 6: 42,341,219 (GRCm39) L535F probably damaging Het
Epha4 A T 1: 77,376,353 (GRCm39) Y509N probably damaging Het
Fads2b T C 2: 85,330,548 (GRCm39) probably benign Het
Ggcx G A 6: 72,403,541 (GRCm39) G363R probably benign Het
Hjurp G C 1: 88,204,937 (GRCm39) probably benign Het
Kpna1 A T 16: 35,823,252 (GRCm39) T35S probably benign Het
Map3k20 T G 2: 72,268,644 (GRCm39) I550M probably damaging Het
Mgat4a A G 1: 37,489,495 (GRCm39) probably benign Het
Mrpl48 T A 7: 100,209,130 (GRCm39) probably benign Het
Ncapd2 T C 6: 125,163,747 (GRCm39) K78E probably damaging Het
Ndst1 T C 18: 60,830,211 (GRCm39) N633S probably benign Het
Or10a3n C A 7: 108,493,189 (GRCm39) V142L probably benign Het
Or5w10 T C 2: 87,375,409 (GRCm39) T160A probably damaging Het
Or6c69 A G 10: 129,747,505 (GRCm39) I214T probably benign Het
Pacs2 T C 12: 113,024,733 (GRCm39) S408P probably damaging Het
Pcx C T 19: 4,667,995 (GRCm39) H506Y probably benign Het
Pla2g6 G T 15: 79,197,296 (GRCm39) P93T probably damaging Het
Pramel28 C T 4: 143,692,356 (GRCm39) W215* probably null Het
Prb1b G A 6: 132,289,657 (GRCm39) P56S unknown Het
Rcor1 A G 12: 111,006,169 (GRCm39) probably benign Het
Rtn4ip1 T A 10: 43,785,893 (GRCm39) probably null Het
Sytl2 T A 7: 90,030,700 (GRCm39) probably benign Het
Tia1 T C 6: 86,393,319 (GRCm39) F53S probably damaging Het
Ticrr T C 7: 79,331,817 (GRCm39) L776S probably damaging Het
Tmod1 A G 4: 46,078,315 (GRCm39) N41S probably damaging Het
Ttn T C 2: 76,583,139 (GRCm39) I22585V possibly damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Ugt1a10 C A 1: 88,143,862 (GRCm39) H361N probably damaging Het
Vps39 C T 2: 120,180,656 (GRCm39) R43Q probably benign Het
Vwa5b2 T C 16: 20,417,111 (GRCm39) *603Q probably null Het
Zeb1 G A 18: 5,772,716 (GRCm39) A1002T probably benign Het
Zxdc A G 6: 90,347,449 (GRCm39) probably null Het
Other mutations in Vmn1r118
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4061:Vmn1r118 UTSW 7 20,645,933 (GRCm39) missense probably damaging 0.96
R4062:Vmn1r118 UTSW 7 20,645,933 (GRCm39) missense probably damaging 0.96
R9253:Vmn1r118 UTSW 7 20,645,817 (GRCm39) missense possibly damaging 0.53
Predicted Primers PCR Primer
(F):5'- GCCTACAATGAATCCAGAAGTGG -3'
(R):5'- GACCCAGACAGGTGATTTTAAGC -3'

Sequencing Primer
(F):5'- GTGGAACAGAACAAGTTGCTTTTAG -3'
(R):5'- CCAGACAGGTGATTTTAAGCCACATG -3'
Posted On 2015-04-17