Incidental Mutation 'R6681:Vmn1r45'
ID 527496
Institutional Source Beutler Lab
Gene Symbol Vmn1r45
Ensembl Gene ENSMUSG00000044248
Gene Name vomeronasal 1 receptor 45
Synonyms V1ra2, V1r2
MMRRC Submission 044800-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # R6681 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 89908632-89917489 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to A at 89910985 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000154795 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054202] [ENSMUST00000226167] [ENSMUST00000227122] [ENSMUST00000227426] [ENSMUST00000227571] [ENSMUST00000227977] [ENSMUST00000228662] [ENSMUST00000228492]
AlphaFold Q8VIC7
Predicted Effect probably benign
Transcript: ENSMUST00000054202
SMART Domains Protein: ENSMUSP00000052123
Gene: ENSMUSG00000044248

DomainStartEndE-ValueType
Pfam:TAS2R 26 315 2.5e-10 PFAM
Pfam:V1R 54 318 1.5e-136 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226167
Predicted Effect probably benign
Transcript: ENSMUST00000227122
Predicted Effect probably benign
Transcript: ENSMUST00000227426
Predicted Effect probably benign
Transcript: ENSMUST00000227571
Predicted Effect probably benign
Transcript: ENSMUST00000227977
Predicted Effect probably benign
Transcript: ENSMUST00000228662
Predicted Effect probably benign
Transcript: ENSMUST00000228492
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.4%
  • 20x: 95.6%
Validation Efficiency 98% (45/46)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 A T 3: 121,915,447 (GRCm39) T971S probably damaging Het
Catsperb C T 12: 101,590,994 (GRCm39) Q1021* probably null Het
Ccdc62 A G 5: 124,072,156 (GRCm39) T62A probably benign Het
Cuzd1 A G 7: 130,913,412 (GRCm39) S402P probably damaging Het
Dcun1d1 C T 3: 35,949,819 (GRCm39) V244M probably damaging Het
Dennd2c A G 3: 103,038,977 (GRCm39) T42A probably benign Het
Dnah7a T C 1: 53,560,385 (GRCm39) probably null Het
Dnase1l1 C T X: 73,320,644 (GRCm39) probably null Homo
Dpp4 A T 2: 62,178,893 (GRCm39) F607L probably benign Het
Ech1 C T 7: 28,529,763 (GRCm39) probably null Het
Fam53a A G 5: 33,765,184 (GRCm39) L174P probably damaging Het
Fh1 T C 1: 175,446,690 (GRCm39) D62G probably null Het
Gpatch11 T C 17: 79,147,528 (GRCm39) I103T probably damaging Het
Hmgcll1 A T 9: 75,988,731 (GRCm39) T169S probably benign Het
Kbtbd3 A T 9: 4,330,687 (GRCm39) I354F probably benign Het
Kdm5b T C 1: 134,541,007 (GRCm39) F700L possibly damaging Het
Mamdc4 C A 2: 25,457,756 (GRCm39) G439V probably damaging Het
Mrps30 A T 13: 118,517,134 (GRCm39) S362T probably damaging Het
Mug1 C T 6: 121,815,683 (GRCm39) S29L possibly damaging Het
Myh2 G A 11: 67,069,174 (GRCm39) D328N probably damaging Het
Or10j3b C A 1: 173,043,973 (GRCm39) H252N probably damaging Het
Or5b98 A G 19: 12,931,823 (GRCm39) Y290C probably damaging Het
Or5j1 T C 2: 86,878,942 (GRCm39) T213A probably benign Het
Or8g54 T A 9: 39,706,710 (GRCm39) I13N probably benign Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Pira13 T A 7: 3,825,251 (GRCm39) M464L probably benign Het
Pus7l G A 15: 94,425,746 (GRCm39) P552S probably benign Het
Rest A G 5: 77,428,844 (GRCm39) K421R probably damaging Het
Rttn C A 18: 89,032,735 (GRCm39) H668N probably damaging Het
Scn9a T C 2: 66,393,686 (GRCm39) I228V possibly damaging Het
Scp2 G T 4: 107,948,513 (GRCm39) Q155K probably damaging Het
Sec61a2 G A 2: 5,881,219 (GRCm39) R18* probably null Het
Serpinb8 T A 1: 107,525,321 (GRCm39) M41K probably damaging Het
Sgsm2 A T 11: 74,756,204 (GRCm39) W382R probably damaging Het
Slc26a10 G T 10: 127,009,530 (GRCm39) T606N possibly damaging Het
Slc30a6 T C 17: 74,711,027 (GRCm39) I40T possibly damaging Het
Slfn5 G A 11: 82,847,204 (GRCm39) E30K possibly damaging Het
Sorcs2 C A 5: 36,555,154 (GRCm39) R79L probably benign Het
Tmc5 G A 7: 118,268,527 (GRCm39) S865N probably damaging Het
Tmprss11c T A 5: 86,437,119 (GRCm39) M1L possibly damaging Het
Trpv5 C G 6: 41,630,288 (GRCm39) E601Q probably damaging Het
Ttc39b A T 4: 83,158,285 (GRCm39) probably benign Het
Ttll6 T A 11: 96,029,689 (GRCm39) C201S probably damaging Het
Vezt A G 10: 93,832,859 (GRCm39) V204A probably benign Het
Zfp433 A T 10: 81,556,722 (GRCm39) H408L probably damaging Het
Zfp865 T C 7: 5,032,450 (GRCm39) I145T possibly damaging Het
Other mutations in Vmn1r45
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00264:Vmn1r45 APN 6 89,910,646 (GRCm39) missense probably damaging 1.00
IGL02010:Vmn1r45 APN 6 89,910,668 (GRCm39) missense probably damaging 1.00
IGL02124:Vmn1r45 APN 6 89,910,035 (GRCm39) missense probably benign 0.03
IGL02413:Vmn1r45 APN 6 89,910,503 (GRCm39) missense possibly damaging 0.75
R0123:Vmn1r45 UTSW 6 89,910,492 (GRCm39) nonsense probably null
R0225:Vmn1r45 UTSW 6 89,910,492 (GRCm39) nonsense probably null
R1513:Vmn1r45 UTSW 6 89,910,058 (GRCm39) missense probably damaging 0.97
R2154:Vmn1r45 UTSW 6 89,910,965 (GRCm39) missense possibly damaging 0.91
R3082:Vmn1r45 UTSW 6 89,910,724 (GRCm39) missense probably benign 0.03
R3781:Vmn1r45 UTSW 6 89,910,799 (GRCm39) missense probably benign
R4982:Vmn1r45 UTSW 6 89,910,847 (GRCm39) missense probably damaging 0.99
R5086:Vmn1r45 UTSW 6 89,910,082 (GRCm39) missense probably benign 0.06
R5327:Vmn1r45 UTSW 6 89,910,123 (GRCm39) missense possibly damaging 0.79
R5470:Vmn1r45 UTSW 6 89,910,698 (GRCm39) missense probably benign 0.04
R7046:Vmn1r45 UTSW 6 89,910,538 (GRCm39) missense probably benign 0.00
R7050:Vmn1r45 UTSW 6 89,910,703 (GRCm39) missense probably damaging 0.97
R7171:Vmn1r45 UTSW 6 89,910,316 (GRCm39) missense probably damaging 1.00
R7236:Vmn1r45 UTSW 6 89,910,133 (GRCm39) missense probably benign 0.15
R7401:Vmn1r45 UTSW 6 89,910,416 (GRCm39) missense possibly damaging 0.64
R7417:Vmn1r45 UTSW 6 89,910,035 (GRCm39) missense probably benign 0.03
R8068:Vmn1r45 UTSW 6 89,910,261 (GRCm39) missense possibly damaging 0.53
R8223:Vmn1r45 UTSW 6 89,910,074 (GRCm39) missense probably damaging 0.99
R8942:Vmn1r45 UTSW 6 89,910,876 (GRCm39) missense probably benign 0.00
RF019:Vmn1r45 UTSW 6 89,910,091 (GRCm39) missense probably damaging 0.99
X0026:Vmn1r45 UTSW 6 89,910,724 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TCAGTGAGTCTGAGCCTGTG -3'
(R):5'- AGTAAGATGCTCCAGGAAAACC -3'

Sequencing Primer
(F):5'- CCTGTGTCCACGAATGAACTTTAGG -3'
(R):5'- GATGCTCCAGGAAAACCTACACATG -3'
Posted On 2018-07-23