Incidental Mutation 'R9402:Vmn1r43'
ID 711283
Institutional Source Beutler Lab
Gene Symbol Vmn1r43
Ensembl Gene ENSMUSG00000068231
Gene Name vomeronasal 1 receptor 43
Synonyms V1ra5
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R9402 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 89858934-89876413 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to A at 89869895 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Threonine to Methionine at position 203 (T203M)
Ref Sequence ENSEMBL: ENSMUSP00000086839 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089418] [ENSMUST00000226741] [ENSMUST00000226983] [ENSMUST00000227279] [ENSMUST00000228709]
AlphaFold Q8VIC9
Predicted Effect probably damaging
Transcript: ENSMUST00000089418
AA Change: T203M

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000086839
Gene: ENSMUSG00000068231
AA Change: T203M

DomainStartEndE-ValueType
Pfam:V1R 54 318 2.9e-126 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000226741
AA Change: T203M

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000226983
AA Change: T203M

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably benign
Transcript: ENSMUST00000227279
Predicted Effect probably damaging
Transcript: ENSMUST00000228709
AA Change: T203M

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Meta Mutation Damage Score 0.6329 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730559C18Rik T G 1: 136,227,610 S86R probably benign Het
Abca9 T A 11: 110,158,328 Q218L probably benign Het
Atg2b A G 12: 105,648,423 F1083S probably damaging Het
Bche T C 3: 73,701,323 N257D probably benign Het
Cfap221 T A 1: 119,932,821 M692L probably benign Het
Cfap46 G T 7: 139,635,949 P1530Q unknown Het
Crim1 CCGC CC 17: 78,350,865 probably null Het
Cyp4f39 T C 17: 32,491,209 probably null Het
Daam1 A G 12: 71,959,830 T674A probably benign Het
Elp2 A T 18: 24,626,163 I526L probably benign Het
Exoc4 T A 6: 33,476,143 *523K probably null Het
Fbxl7 G A 15: 26,552,503 S226L probably damaging Het
Fry G A 5: 150,433,696 E1903K possibly damaging Het
Fry G A 5: 150,436,853 R1988K probably damaging Het
Gas1 A T 13: 60,176,202 M206K probably damaging Het
Gbp10 T A 5: 105,233,997 T96S possibly damaging Het
Gm14569 G A X: 36,430,896 P1387S probably damaging Het
Gpaa1 A G 15: 76,332,218 T105A probably benign Het
Hoxc13 C A 15: 102,921,616 C143* probably null Het
Htt T C 5: 34,848,980 I1411T probably damaging Het
Jmy C T 13: 93,499,170 C46Y probably damaging Het
Klhl40 A G 9: 121,780,416 Y453C possibly damaging Het
Krit1 T A 5: 3,822,210 Y460N possibly damaging Het
Lamb3 C A 1: 193,331,396 T526K Het
Lrrc29 T A 8: 105,323,356 Y12F probably benign Het
Luzp1 T A 4: 136,543,182 H905Q probably damaging Het
Lyst T A 13: 13,637,878 H958Q probably benign Het
Magi1 T C 6: 94,283,297 N9S probably benign Het
Mmadhc A T 2: 50,281,107 V231E probably benign Het
Muc5b T A 7: 141,845,414 M364K unknown Het
Nae1 A G 8: 104,528,185 probably null Het
Ndst4 C T 3: 125,724,736 S354L probably benign Het
Nlgn2 A G 11: 69,828,107 F252S Het
Nlrp9a A T 7: 26,570,605 N874I possibly damaging Het
Nodal T C 10: 61,423,600 I272T probably damaging Het
Olfr1234 C A 2: 89,362,779 G217* probably null Het
Olfr1259 A T 2: 89,943,940 Y58* probably null Het
Olfr599 T C 7: 103,338,989 S312P probably benign Het
Olfr645 G A 7: 104,084,403 R226* probably null Het
Orm1 C A 4: 63,345,132 Q61K possibly damaging Het
Pcdh17 T C 14: 84,447,206 V371A probably damaging Het
Pcdhb19 C T 18: 37,499,479 Q776* probably null Het
Phf14 A G 6: 11,933,780 R214G possibly damaging Het
Phf3 G A 1: 30,811,847 T1142M probably damaging Het
Pigz A G 16: 31,945,369 E415G probably damaging Het
Pramel5 T C 4: 144,271,456 T406A probably benign Het
Prtg A G 9: 72,911,971 E1082G probably benign Het
Rtp3 A G 9: 110,985,963 C445R unknown Het
Scn3b A T 9: 40,282,556 E193V probably damaging Het
Scn7a A T 2: 66,680,112 N1315K probably damaging Het
Snx14 C T 9: 88,407,437 G254D probably damaging Het
Srbd1 T C 17: 86,099,277 D560G probably benign Het
Srp72 T A 5: 76,976,482 L65* probably null Het
Steap1 T A 5: 5,740,664 I95F Het
Taf3 A G 2: 9,951,112 probably null Het
Taok2 T C 7: 126,870,228 N1143D Het
Tas2r114 C T 6: 131,689,931 G45S possibly damaging Het
Tcerg1l T C 7: 138,209,822 K548E probably damaging Het
Tcp1 T A 17: 12,922,618 L328Q probably benign Het
Tns2 A G 15: 102,113,188 H1096R probably damaging Het
Trps1 A T 15: 50,846,256 Y233N probably damaging Het
Tubgcp6 A G 15: 89,102,861 V1303A probably benign Het
Ugt1a2 T C 1: 88,200,962 F109S possibly damaging Het
Zfp748 A G 13: 67,545,392 V54A probably benign Het
Other mutations in Vmn1r43
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01748:Vmn1r43 APN 6 89870312 missense probably damaging 1.00
IGL02476:Vmn1r43 APN 6 89870061 missense possibly damaging 0.95
IGL02958:Vmn1r43 APN 6 89870049 missense probably benign 0.09
R0413:Vmn1r43 UTSW 6 89869848 missense probably damaging 1.00
R1662:Vmn1r43 UTSW 6 89869590 missense possibly damaging 0.76
R1668:Vmn1r43 UTSW 6 89869701 missense probably benign 0.01
R4419:Vmn1r43 UTSW 6 89869647 missense probably benign 0.01
R4719:Vmn1r43 UTSW 6 89869855 missense probably benign 0.02
R4798:Vmn1r43 UTSW 6 89869910 missense probably benign 0.01
R5520:Vmn1r43 UTSW 6 89869746 missense probably damaging 0.98
R5643:Vmn1r43 UTSW 6 89870372 missense probably damaging 1.00
R5644:Vmn1r43 UTSW 6 89870372 missense probably damaging 1.00
R5717:Vmn1r43 UTSW 6 89869923 missense probably damaging 1.00
R6647:Vmn1r43 UTSW 6 89869859 missense probably damaging 1.00
R6914:Vmn1r43 UTSW 6 89870337 missense probably benign 0.02
R6942:Vmn1r43 UTSW 6 89870337 missense probably benign 0.02
R7092:Vmn1r43 UTSW 6 89869903 missense probably benign 0.02
R7402:Vmn1r43 UTSW 6 89869821 missense probably benign 0.02
R7457:Vmn1r43 UTSW 6 89870190 missense probably damaging 0.98
R7572:Vmn1r43 UTSW 6 89869565 missense possibly damaging 0.93
R7807:Vmn1r43 UTSW 6 89870237 missense probably benign 0.07
R8406:Vmn1r43 UTSW 6 89870432 missense possibly damaging 0.55
R8696:Vmn1r43 UTSW 6 89870339 missense probably damaging 0.99
R8859:Vmn1r43 UTSW 6 89869955 missense probably damaging 1.00
R8894:Vmn1r43 UTSW 6 89869764 missense probably benign 0.02
R9072:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9073:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9075:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9076:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9237:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9239:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9240:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9293:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9383:Vmn1r43 UTSW 6 89869570 missense possibly damaging 0.94
R9398:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9399:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9401:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9594:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9595:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9596:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9624:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9628:Vmn1r43 UTSW 6 89869895 missense probably damaging 1.00
R9656:Vmn1r43 UTSW 6 89870458 missense possibly damaging 0.47
X0020:Vmn1r43 UTSW 6 89870334 missense probably benign 0.00
Z1177:Vmn1r43 UTSW 6 89870485 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GGTCATGAGCATCAGGATGG -3'
(R):5'- CCATCATTCTTAGTCCCAGAAGC -3'

Sequencing Primer
(F):5'- CATCAGGATGGTCTGGGTAGCAC -3'
(R):5'- GTCCCAGAAGCTCCTGTTTATCAAAG -3'
Posted On 2022-05-16