Incidental Mutation 'R3025:Vmn1r57'
ID 265798
Institutional Source Beutler Lab
Gene Symbol Vmn1r57
Ensembl Gene ENSMUSG00000091652
Gene Name vomeronasal 1 receptor 57
Synonyms Gm7519
MMRRC Submission 040541-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # R3025 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 5223477-5224409 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 5223714 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 80 (K80*)
Ref Sequence ENSEMBL: ENSMUSP00000153848 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170780] [ENSMUST00000227798] [ENSMUST00000228062]
AlphaFold K7N731
Predicted Effect probably null
Transcript: ENSMUST00000170780
AA Change: K80*
SMART Domains Protein: ENSMUSP00000131917
Gene: ENSMUSG00000091652
AA Change: K80*

DomainStartEndE-ValueType
Pfam:TAS2R 1 290 1.7e-12 PFAM
Pfam:7tm_1 20 279 1.8e-6 PFAM
Pfam:V1R 32 289 1.1e-19 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000227798
AA Change: K80*
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227864
Predicted Effect probably null
Transcript: ENSMUST00000228062
AA Change: K80*
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ace T A 11: 105,864,919 (GRCm39) probably null Het
Akap6 A G 12: 53,186,926 (GRCm39) T1447A probably benign Het
Atp13a2 C T 4: 140,721,659 (GRCm39) R250C probably damaging Het
Cacna1a T A 8: 85,306,854 (GRCm39) probably null Het
Chd6 GATCAT GAT 2: 160,808,472 (GRCm39) probably benign Het
Cptp T C 4: 155,951,678 (GRCm39) E5G possibly damaging Het
Dnajc16 C A 4: 141,501,922 (GRCm39) V303F probably benign Het
Gm10842 T C 11: 105,037,902 (GRCm39) S62P unknown Het
Gm17509 T C 13: 117,357,112 (GRCm39) probably benign Het
Homer1 C T 13: 93,538,582 (GRCm39) Q142* probably null Het
Kcnb2 C A 1: 15,781,059 (GRCm39) Q644K possibly damaging Het
Map3k19 T C 1: 127,766,290 (GRCm39) probably null Het
Msh4 T A 3: 153,569,128 (GRCm39) H621L probably damaging Het
Ogfod1 A T 8: 94,789,680 (GRCm39) E460D probably damaging Het
Or6c65 T A 10: 129,603,542 (GRCm39) F59Y probably damaging Het
Or8k41 A T 2: 86,314,083 (GRCm39) M1K probably null Het
Rp1 G A 1: 4,422,898 (GRCm39) R61W probably damaging Het
Scaf4 A T 16: 90,048,826 (GRCm39) H329Q unknown Het
Sec61a1 A T 6: 88,489,202 (GRCm39) D166E probably damaging Het
Tars2 C T 3: 95,654,952 (GRCm39) R63H possibly damaging Het
Vmn2r106 A G 17: 20,499,147 (GRCm39) W255R probably benign Het
Wdr49 C G 3: 75,240,663 (GRCm39) C402S possibly damaging Het
Other mutations in Vmn1r57
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01770:Vmn1r57 APN 7 5,223,667 (GRCm39) missense possibly damaging 0.61
IGL03124:Vmn1r57 APN 7 5,224,021 (GRCm39) missense possibly damaging 0.91
R1779:Vmn1r57 UTSW 7 5,223,576 (GRCm39) missense possibly damaging 0.89
R3917:Vmn1r57 UTSW 7 5,223,630 (GRCm39) missense probably damaging 1.00
R4093:Vmn1r57 UTSW 7 5,223,856 (GRCm39) missense possibly damaging 0.80
R4552:Vmn1r57 UTSW 7 5,223,667 (GRCm39) missense possibly damaging 0.61
R4628:Vmn1r57 UTSW 7 5,223,972 (GRCm39) missense probably damaging 1.00
R5186:Vmn1r57 UTSW 7 5,224,107 (GRCm39) missense probably benign 0.08
R5290:Vmn1r57 UTSW 7 5,224,319 (GRCm39) missense probably damaging 1.00
R5559:Vmn1r57 UTSW 7 5,223,898 (GRCm39) missense probably damaging 1.00
R6372:Vmn1r57 UTSW 7 5,223,826 (GRCm39) missense possibly damaging 0.61
R7105:Vmn1r57 UTSW 7 5,223,499 (GRCm39) missense probably damaging 1.00
R7220:Vmn1r57 UTSW 7 5,223,559 (GRCm39) missense probably null 1.00
R7835:Vmn1r57 UTSW 7 5,224,138 (GRCm39) missense probably benign 0.44
R7872:Vmn1r57 UTSW 7 5,223,613 (GRCm39) missense possibly damaging 0.48
R8310:Vmn1r57 UTSW 7 5,224,024 (GRCm39) missense probably damaging 1.00
R9679:Vmn1r57 UTSW 7 5,224,230 (GRCm39) missense probably benign 0.09
R9681:Vmn1r57 UTSW 7 5,224,069 (GRCm39) missense probably damaging 0.99
X0064:Vmn1r57 UTSW 7 5,223,760 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGGCAACATCCTTCTGTTTGTC -3'
(R):5'- CTGTGGACCACTGACATTCATTG -3'

Sequencing Primer
(F):5'- GTCCATAACTTCTCTCCAAACTTGAC -3'
(R):5'- CCACTGACATTCATTGGGATGTAAGC -3'
Posted On 2015-02-05