Incidental Mutation 'R7285:Vmn1r233'
ID565961
Institutional Source Beutler Lab
Gene Symbol Vmn1r233
Ensembl Gene ENSMUSG00000045575
Gene Namevomeronasal 1 receptor 233
SynonymsV1rf5
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.061) question?
Stock #R7285 (G1)
Quality Score225.009
Status Validated
Chromosome17
Chromosomal Location20993727-20994686 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 20993959 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Threonine at position 243 (I243T)
Ref Sequence ENSEMBL: ENSMUSP00000062473 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056339]
Predicted Effect probably damaging
Transcript: ENSMUST00000056339
AA Change: I243T

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000062473
Gene: ENSMUSG00000045575
AA Change: I243T

DomainStartEndE-ValueType
Pfam:TAS2R 8 304 4.8e-11 PFAM
Pfam:7tm_1 11 297 7.9e-7 PFAM
Pfam:V1R 40 303 1.3e-24 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (58/58)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210016F16Rik T C 13: 58,384,385 Y119C probably damaging Het
Abca12 A T 1: 71,349,155 C185* probably null Het
Abcc3 C T 11: 94,357,047 A1207T probably benign Het
Adam1b T G 5: 121,500,993 D663A probably damaging Het
Arhgap12 A T 18: 6,111,920 L148Q probably damaging Het
Cdh4 A T 2: 179,797,465 Q135L probably benign Het
Clca3b T C 3: 144,837,758 I437V probably benign Het
Cldn15 A T 5: 136,972,473 H124L probably benign Het
Cyp4a30b T C 4: 115,456,651 M143T probably damaging Het
Dgcr2 A T 16: 17,845,080 C353* probably null Het
Dhcr24 T A 4: 106,571,519 probably null Het
Dock1 T G 7: 134,745,008 L223R probably benign Het
Ece1 T A 4: 137,913,763 probably null Het
Efcab5 A G 11: 77,137,344 V387A probably benign Het
Efcab5 A G 11: 77,138,215 F97L possibly damaging Het
Eme2 A T 17: 24,894,569 probably null Het
Enpp1 G A 10: 24,660,161 T447I probably benign Het
Fam222b T C 11: 78,143,181 S17P probably benign Het
Fbln1 A G 15: 85,237,628 I317V probably benign Het
Fn1 T C 1: 71,637,339 K578E probably damaging Het
Fscb A T 12: 64,471,549 S1048T unknown Het
Fsd1l T A 4: 53,682,200 probably null Het
Gm340 A G 19: 41,584,315 K503R possibly damaging Het
Hexa T A 9: 59,563,939 I492K probably benign Het
Inpp5e G A 2: 26,397,858 A642V probably benign Het
Ints11 C T 4: 155,886,111 A241V probably damaging Het
Irs2 A G 8: 11,006,797 L545P probably damaging Het
Katnal2 G A 18: 76,993,575 A409V probably benign Het
Kif13a C T 13: 46,752,455 V671M possibly damaging Het
Lbx2 A G 6: 83,087,896 K138R probably damaging Het
Lpp G A 16: 24,977,279 A558T probably damaging Het
Lypla1 T C 1: 4,841,098 I202T probably benign Het
Magi3 G A 3: 104,034,114 P842S probably benign Het
Meioc G A 11: 102,666,342 V25M probably benign Het
Mthfr C T 4: 148,053,599 T557I probably benign Het
Nbeal1 G C 1: 60,237,151 V684L probably benign Het
Olfr1165-ps A T 2: 88,101,705 I94N probably damaging Het
Olfr314 T A 11: 58,786,484 Y83* probably null Het
Osbpl10 A T 9: 115,223,703 I440F probably damaging Het
Otx2 G A 14: 48,661,465 A36V probably benign Het
Parg A G 14: 32,210,508 Y435C probably damaging Het
Parvb A T 15: 84,282,784 D100V possibly damaging Het
Prss27 A G 17: 24,045,691 H276R probably benign Het
Prune1 T A 3: 95,255,046 S439C probably damaging Het
Pudp C G 18: 50,568,216 E149Q possibly damaging Het
Sin3a C A 9: 57,127,299 T1252N possibly damaging Het
Sptbn2 A G 19: 4,737,443 D927G probably benign Het
Stx18 C T 5: 38,104,907 T89I possibly damaging Het
Ticrr T C 7: 79,660,862 S175P possibly damaging Het
Tinag T C 9: 77,045,661 T14A probably benign Het
Tmco3 G A 8: 13,319,605 probably null Het
Trpm1 G T 7: 64,209,981 E396* probably null Het
Txndc11 A G 16: 11,084,299 Y684H probably damaging Het
Usp47 G A 7: 112,093,108 E926K probably benign Het
Ythdf3 T A 3: 16,203,885 probably null Het
Zfp12 A G 5: 143,244,689 K289R probably damaging Het
Zfp950 T A 19: 61,119,112 H511L probably benign Het
Other mutations in Vmn1r233
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01843:Vmn1r233 APN 17 20994599 missense probably damaging 1.00
IGL01912:Vmn1r233 APN 17 20994205 missense probably benign 0.02
IGL02642:Vmn1r233 APN 17 20994029 missense probably damaging 0.97
IGL02730:Vmn1r233 APN 17 20993795 missense possibly damaging 0.81
IGL02754:Vmn1r233 APN 17 20994625 missense probably benign 0.37
IGL02754:Vmn1r233 APN 17 20994624 missense probably benign
BB008:Vmn1r233 UTSW 17 20993863 missense probably benign
BB018:Vmn1r233 UTSW 17 20993863 missense probably benign
R0368:Vmn1r233 UTSW 17 20994607 missense possibly damaging 0.93
R1894:Vmn1r233 UTSW 17 20993732 missense probably benign 0.02
R2507:Vmn1r233 UTSW 17 20993848 missense probably benign 0.29
R4609:Vmn1r233 UTSW 17 20994415 missense possibly damaging 0.79
R4662:Vmn1r233 UTSW 17 20994131 missense probably benign 0.16
R4686:Vmn1r233 UTSW 17 20994106 missense probably benign 0.33
R4721:Vmn1r233 UTSW 17 20994617 missense probably benign
R5559:Vmn1r233 UTSW 17 20994577 missense possibly damaging 0.74
R5651:Vmn1r233 UTSW 17 20994017 missense probably benign 0.00
R6642:Vmn1r233 UTSW 17 20993740 missense probably damaging 1.00
R7931:Vmn1r233 UTSW 17 20993863 missense probably benign
R7936:Vmn1r233 UTSW 17 20993975 nonsense probably null
R7984:Vmn1r233 UTSW 17 20994155 missense probably damaging 0.99
R8059:Vmn1r233 UTSW 17 20994436 missense probably benign 0.06
Z1176:Vmn1r233 UTSW 17 20994658 missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- CTTTTCAAGGGCAGGCAGAAG -3'
(R):5'- ATGCTGTGCGTCATGATCCAAC -3'

Sequencing Primer
(F):5'- AAGCTGGATGCCCGAGAGTC -3'
(R):5'- TGCGTCATGATCCAACCAGTG -3'
Posted On2019-06-26