Incidental Mutation 'R4460:Vmn1r203'
ID 330112
Institutional Source Beutler Lab
Gene Symbol Vmn1r203
Ensembl Gene ENSMUSG00000069289
Gene Name vomeronasal 1 receptor 203
Synonyms V1rh11
MMRRC Submission 041719-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R4460 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 22708221-22709156 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 22708852 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 211 (M211K)
Ref Sequence ENSEMBL: ENSMUSP00000154399 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091729] [ENSMUST00000227520] [ENSMUST00000228889]
AlphaFold Q8R273
Predicted Effect probably damaging
Transcript: ENSMUST00000091729
AA Change: M211K

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000089322
Gene: ENSMUSG00000069289
AA Change: M211K

DomainStartEndE-ValueType
transmembrane domain 19 41 N/A INTRINSIC
Pfam:V1R 43 304 5.8e-35 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137651
Predicted Effect probably damaging
Transcript: ENSMUST00000227520
AA Change: M211K

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000228889
AA Change: M211K

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Btbd8 A G 5: 107,651,631 (GRCm39) T687A possibly damaging Het
C030048H21Rik A G 2: 26,145,875 (GRCm39) probably null Het
Cav1 A G 6: 17,306,471 (GRCm39) D8G probably damaging Het
Celf6 G A 9: 59,510,327 (GRCm39) R103H probably damaging Het
Ctr9 A G 7: 110,646,101 (GRCm39) I698V probably benign Het
Cts6 G C 13: 61,343,272 (GRCm39) I316M probably benign Het
Dnajc13 C A 9: 104,058,262 (GRCm39) R1496L probably damaging Het
Dscam A G 16: 96,411,519 (GRCm39) Y1786H probably damaging Het
Fcgbpl1 C T 7: 27,852,281 (GRCm39) T1268I probably benign Het
Itga2 C G 13: 114,980,019 (GRCm39) D1061H probably damaging Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Klhl26 T C 8: 70,904,194 (GRCm39) Y538C probably damaging Het
Ltk A G 2: 119,586,094 (GRCm39) probably null Het
Med20 T C 17: 47,929,842 (GRCm39) V93A probably benign Het
Mmp9 G T 2: 164,790,958 (GRCm39) K115N probably damaging Het
Mroh5 A T 15: 73,663,645 (GRCm39) D339E probably damaging Het
Muc1 A T 3: 89,138,870 (GRCm39) D493V probably damaging Het
Mx1 G T 16: 97,255,281 (GRCm39) S113R probably damaging Het
Nlrp9c T A 7: 26,077,523 (GRCm39) H698L probably damaging Het
Nol9 T G 4: 152,142,293 (GRCm39) L641R probably damaging Het
Pla2g4e T G 2: 120,016,863 (GRCm39) H226P possibly damaging Het
Pou2f1 A G 1: 165,722,575 (GRCm39) F337L probably damaging Het
Prkn A T 17: 12,280,533 (GRCm39) D463V probably damaging Het
Ptcd1 G T 5: 145,096,316 (GRCm39) A259E probably benign Het
Ptov1 T C 7: 44,515,000 (GRCm39) M204V probably benign Het
Rasal2 A G 1: 157,003,402 (GRCm39) F419S possibly damaging Het
Rbbp8nl A G 2: 179,922,764 (GRCm39) S210P probably benign Het
Rgmb C A 17: 16,027,888 (GRCm39) R277L probably benign Het
Snx2 A G 18: 53,309,516 (GRCm39) E22G probably benign Het
Snx30 A T 4: 59,885,022 (GRCm39) R221* probably null Het
Tmem143 C T 7: 45,556,376 (GRCm39) T97I probably damaging Het
Ttn A C 2: 76,644,991 (GRCm39) F12955V probably damaging Het
Ubr2 C T 17: 47,255,971 (GRCm39) probably null Het
Vmn2r121 G A X: 123,038,281 (GRCm39) P580S probably benign Het
Zfp804b A T 5: 6,821,481 (GRCm39) D491E probably damaging Het
Other mutations in Vmn1r203
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01356:Vmn1r203 APN 13 22,708,947 (GRCm39) missense probably damaging 1.00
IGL01527:Vmn1r203 APN 13 22,708,447 (GRCm39) missense possibly damaging 0.89
IGL01808:Vmn1r203 APN 13 22,708,717 (GRCm39) missense probably benign 0.02
IGL01887:Vmn1r203 APN 13 22,709,046 (GRCm39) missense probably benign 0.00
IGL02340:Vmn1r203 APN 13 22,708,997 (GRCm39) nonsense probably null
IGL02543:Vmn1r203 APN 13 22,709,074 (GRCm39) missense probably damaging 1.00
IGL02684:Vmn1r203 APN 13 22,708,539 (GRCm39) missense possibly damaging 0.95
BB005:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
BB015:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
PIT4519001:Vmn1r203 UTSW 13 22,708,765 (GRCm39) missense probably benign 0.01
R0544:Vmn1r203 UTSW 13 22,708,443 (GRCm39) missense possibly damaging 0.94
R1365:Vmn1r203 UTSW 13 22,708,756 (GRCm39) missense probably benign 0.00
R1396:Vmn1r203 UTSW 13 22,708,678 (GRCm39) missense probably benign 0.01
R1794:Vmn1r203 UTSW 13 22,708,521 (GRCm39) missense probably damaging 1.00
R2010:Vmn1r203 UTSW 13 22,708,617 (GRCm39) missense possibly damaging 0.56
R2169:Vmn1r203 UTSW 13 22,708,905 (GRCm39) nonsense probably null
R2333:Vmn1r203 UTSW 13 22,709,113 (GRCm39) missense probably damaging 1.00
R2418:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R2419:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R4322:Vmn1r203 UTSW 13 22,708,408 (GRCm39) missense probably damaging 1.00
R4686:Vmn1r203 UTSW 13 22,708,528 (GRCm39) missense probably damaging 1.00
R5526:Vmn1r203 UTSW 13 22,708,273 (GRCm39) missense probably benign 0.01
R6240:Vmn1r203 UTSW 13 22,708,899 (GRCm39) missense possibly damaging 0.89
R6607:Vmn1r203 UTSW 13 22,708,891 (GRCm39) missense probably benign 0.23
R7575:Vmn1r203 UTSW 13 22,708,588 (GRCm39) missense probably benign 0.12
R7928:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
R8375:Vmn1r203 UTSW 13 22,709,154 (GRCm39) makesense probably null
R8421:Vmn1r203 UTSW 13 22,709,154 (GRCm39) makesense probably null
R8424:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense probably damaging 1.00
R8845:Vmn1r203 UTSW 13 22,708,720 (GRCm39) missense possibly damaging 0.81
R8933:Vmn1r203 UTSW 13 22,708,691 (GRCm39) missense possibly damaging 0.69
R8956:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R9493:Vmn1r203 UTSW 13 22,708,423 (GRCm39) missense probably damaging 1.00
Z1177:Vmn1r203 UTSW 13 22,708,579 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- GAACCTAATCCATTCCATTAGAAGC -3'
(R):5'- AAAGTTGCATAACCAAGGGCC -3'

Sequencing Primer
(F):5'- TCCATTCCATTAGAAGCACAAGTCTG -3'
(R):5'- GGGCCAGAAAATTTCGAGTGTTTAC -3'
Posted On 2015-07-21