Incidental Mutation 'R6439:Vmn1r183'
ID 518935
Institutional Source Beutler Lab
Gene Symbol Vmn1r183
Ensembl Gene ENSMUSG00000066723
Gene Name vomeronasal 1 receptor 183
Synonyms V1rd15, LOC209824
MMRRC Submission 044577-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R6439 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 23754199-23755116 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 23754704 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 169 (D169G)
Ref Sequence ENSEMBL: ENSMUSP00000083176 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086012]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000086012
AA Change: D169G

PolyPhen 2 Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000083176
Gene: ENSMUSG00000066723
AA Change: D169G

DomainStartEndE-ValueType
Pfam:TAS2R 8 297 5.6e-15 PFAM
Pfam:7tm_1 31 285 1.4e-9 PFAM
Pfam:V1R 41 296 2.5e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205855
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.5%
Validation Efficiency 100% (35/35)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130401M01Rik T C 15: 57,895,444 (GRCm39) D18G probably null Het
A530064D06Rik A G 17: 48,473,653 (GRCm39) V88A probably damaging Het
Abhd6 T C 14: 8,055,589 (GRCm38) L272P probably damaging Het
Adam25 C T 8: 41,207,627 (GRCm39) R298C possibly damaging Het
Adam34l T C 8: 44,078,988 (GRCm39) N412S probably damaging Het
Afap1l2 T C 19: 56,916,818 (GRCm39) N219D possibly damaging Het
Brd3 A G 2: 27,353,938 (GRCm39) F58S probably damaging Het
Ceacam3 G A 7: 16,892,253 (GRCm39) R332H possibly damaging Het
Cfap57 C A 4: 118,446,172 (GRCm39) probably null Het
Chd2 A G 7: 73,130,154 (GRCm39) F834L probably damaging Het
Crocc2 A G 1: 93,111,126 (GRCm39) K140E possibly damaging Het
Fam117b A G 1: 60,020,731 (GRCm39) T534A probably benign Het
Fchsd1 C T 18: 38,102,487 (GRCm39) V14I probably damaging Het
Grid2ip A T 5: 143,359,257 (GRCm39) E291V probably damaging Het
Hbp1 A G 12: 31,987,720 (GRCm39) L146S probably damaging Het
Hr A G 14: 70,799,276 (GRCm39) D616G possibly damaging Het
Igfbp5 A C 1: 72,902,300 (GRCm39) probably null Het
Jak2 C T 19: 29,287,022 (GRCm39) probably null Het
Mpl T C 4: 118,305,750 (GRCm39) D425G probably damaging Het
Ms4a4c T C 19: 11,398,676 (GRCm39) S165P probably benign Het
Mycbp2 A G 14: 103,392,911 (GRCm39) S3217P probably benign Het
Nfatc3 T A 8: 106,810,502 (GRCm39) L426* probably null Het
Or4f47 T C 2: 111,972,509 (GRCm39) V73A probably benign Het
Or5ak24 T C 2: 85,261,068 (GRCm39) Y35C probably damaging Het
Or7a42 T A 10: 78,791,818 (GRCm39) Y260N probably damaging Het
Phf1 G T 17: 27,155,586 (GRCm39) V384L probably benign Het
Rangap1 T C 15: 81,596,336 (GRCm39) T259A probably benign Het
Rec8 A G 14: 55,856,076 (GRCm39) N6S possibly damaging Het
Rmdn2 G A 17: 79,934,971 (GRCm39) probably benign Het
Scin T C 12: 40,118,945 (GRCm39) Y617C probably damaging Het
Ttc13 T C 8: 125,400,221 (GRCm39) S744G probably benign Het
Ttc14 T C 3: 33,862,968 (GRCm39) probably benign Het
Uggt1 T C 1: 36,214,032 (GRCm39) E219G possibly damaging Het
Vmn1r72 A T 7: 11,413,064 (GRCm39) probably null Het
Zfp326 T G 5: 106,036,584 (GRCm39) M76R probably null Het
Other mutations in Vmn1r183
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00987:Vmn1r183 APN 7 23,754,649 (GRCm39) missense probably damaging 1.00
IGL01813:Vmn1r183 APN 7 23,754,985 (GRCm39) missense probably benign 0.19
IGL03377:Vmn1r183 APN 7 23,754,817 (GRCm39) missense possibly damaging 0.70
PIT4791001:Vmn1r183 UTSW 7 23,754,266 (GRCm39) missense probably damaging 0.99
R0463:Vmn1r183 UTSW 7 23,754,926 (GRCm39) missense probably damaging 1.00
R0616:Vmn1r183 UTSW 7 23,754,250 (GRCm39) missense probably benign 0.03
R0666:Vmn1r183 UTSW 7 23,754,601 (GRCm39) missense probably benign
R3928:Vmn1r183 UTSW 7 23,754,997 (GRCm39) missense probably damaging 0.98
R4425:Vmn1r183 UTSW 7 23,754,973 (GRCm39) missense probably benign 0.00
R4767:Vmn1r183 UTSW 7 23,754,531 (GRCm39) frame shift probably null
R4835:Vmn1r183 UTSW 7 23,754,564 (GRCm39) missense probably benign 0.07
R5267:Vmn1r183 UTSW 7 23,754,971 (GRCm39) missense possibly damaging 0.90
R5693:Vmn1r183 UTSW 7 23,754,227 (GRCm39) missense possibly damaging 0.94
R6291:Vmn1r183 UTSW 7 23,754,982 (GRCm39) missense possibly damaging 0.70
R7073:Vmn1r183 UTSW 7 23,754,926 (GRCm39) missense probably damaging 1.00
R8732:Vmn1r183 UTSW 7 23,754,890 (GRCm39) missense possibly damaging 0.89
Predicted Primers PCR Primer
(F):5'- TGTTCCACCTGTGTCCTGAG -3'
(R):5'- TTGGTTGCTCTGGACTCAGC -3'

Sequencing Primer
(F):5'- ACCTGTGTCCTGAGTATCCATCAG -3'
(R):5'- TGGACTCAGCTTGGCCTCTG -3'
Posted On 2018-05-24