Incidental Mutation 'R3723:Vmn2r91'
ID 270647
Institutional Source Beutler Lab
Gene Symbol Vmn2r91
Ensembl Gene ENSMUSG00000091206
Gene Name vomeronasal 2, receptor 91
Synonyms EG665210
MMRRC Submission 040714-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R3723 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 18305319-18356905 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to A at 18305540 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127465 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172359]
AlphaFold E9Q2U5
Predicted Effect probably null
Transcript: ENSMUST00000172359
SMART Domains Protein: ENSMUSP00000127465
Gene: ENSMUSG00000091206

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:ANF_receptor 83 462 2.2e-38 PFAM
Pfam:NCD3G 510 564 6.7e-20 PFAM
Pfam:7tm_3 597 832 2.1e-53 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 95% (38/40)
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahnak T C 19: 8,994,217 (GRCm39) V5167A possibly damaging Het
Ano5 A G 7: 51,226,276 (GRCm39) Y510C probably damaging Het
Api5 C T 2: 94,255,958 (GRCm39) R243Q possibly damaging Het
Apob A T 12: 8,056,327 (GRCm39) Q1570L probably damaging Het
Apob A G 12: 8,061,763 (GRCm39) N3415S possibly damaging Het
Arsk T A 13: 76,214,772 (GRCm39) I361F probably damaging Het
C9 G A 15: 6,512,561 (GRCm39) E228K possibly damaging Het
Celsr2 A G 3: 108,304,731 (GRCm39) probably benign Het
Cfap53 A G 18: 74,492,640 (GRCm39) I455V probably benign Het
Ckap4 A G 10: 84,364,256 (GRCm39) L269P probably damaging Het
Dnah7a T A 1: 53,486,505 (GRCm39) D3352V probably benign Het
Dync2h1 A T 9: 7,041,658 (GRCm39) M3335K probably benign Het
Fam171a1 A G 2: 3,221,412 (GRCm39) probably benign Het
Glis3 A T 19: 28,239,991 (GRCm39) C97* probably null Het
Gm14221 C G 2: 160,410,347 (GRCm39) noncoding transcript Het
Gm8603 A C 17: 13,737,075 (GRCm39) probably null Het
Gm9767 G T 10: 25,954,469 (GRCm39) probably benign Het
Kctd16 A G 18: 40,391,912 (GRCm39) T167A possibly damaging Het
Kif18b A G 11: 102,807,102 (GRCm39) F78L probably damaging Het
Mefv A G 16: 3,526,058 (GRCm39) probably null Het
Mipol1 C A 12: 57,503,878 (GRCm39) L349I probably damaging Het
Myo10 T C 15: 25,803,374 (GRCm39) V1527A probably damaging Het
Naip5 G T 13: 100,359,522 (GRCm39) Y571* probably null Het
Npl A G 1: 153,391,210 (GRCm39) F182L probably benign Het
Pan3 T A 5: 147,440,018 (GRCm39) probably benign Het
Pcdh15 A T 10: 74,481,680 (GRCm39) T342S probably benign Het
Pcdhga1 A G 18: 37,796,045 (GRCm39) T350A possibly damaging Het
Pramel28 T C 4: 143,693,251 (GRCm39) T76A probably benign Het
Prdm4 A G 10: 85,735,145 (GRCm39) S666P probably damaging Het
Rere A G 4: 150,553,252 (GRCm39) E148G probably damaging Het
Scube2 T C 7: 109,407,613 (GRCm39) probably benign Het
Sptbn1 A G 11: 30,087,335 (GRCm39) S1035P possibly damaging Het
Srsf4 C T 4: 131,627,413 (GRCm39) probably benign Het
Supt3 A G 17: 45,305,274 (GRCm39) D108G probably damaging Het
Tnfsf13b A G 8: 10,081,545 (GRCm39) I236V possibly damaging Het
Tns1 T C 1: 73,964,099 (GRCm39) S1511G probably damaging Het
Tpm1 G A 9: 66,939,227 (GRCm39) probably benign Het
Uba6 T C 5: 86,282,906 (GRCm39) D559G probably damaging Het
Vmn1r117 T A 7: 20,617,380 (GRCm39) I223F probably damaging Het
Zfp30 A G 7: 29,492,778 (GRCm39) E344G probably damaging Het
Other mutations in Vmn2r91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00983:Vmn2r91 APN 17 18,325,820 (GRCm39) missense probably benign 0.00
IGL01121:Vmn2r91 APN 17 18,356,766 (GRCm39) missense possibly damaging 0.94
IGL01464:Vmn2r91 APN 17 18,327,864 (GRCm39) missense probably null 0.00
IGL02003:Vmn2r91 APN 17 18,327,921 (GRCm39) missense probably benign
IGL02709:Vmn2r91 APN 17 18,325,711 (GRCm39) missense possibly damaging 0.74
IGL02795:Vmn2r91 APN 17 18,305,539 (GRCm39) missense probably benign 0.01
IGL02813:Vmn2r91 APN 17 18,356,348 (GRCm39) missense possibly damaging 0.91
IGL02830:Vmn2r91 APN 17 18,356,884 (GRCm39) missense probably benign 0.01
IGL03130:Vmn2r91 APN 17 18,330,373 (GRCm39) splice site probably benign
BB006:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
BB016:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R0164:Vmn2r91 UTSW 17 18,326,399 (GRCm39) missense probably benign 0.00
R0164:Vmn2r91 UTSW 17 18,326,399 (GRCm39) missense probably benign 0.00
R0393:Vmn2r91 UTSW 17 18,325,712 (GRCm39) missense probably damaging 1.00
R1142:Vmn2r91 UTSW 17 18,356,705 (GRCm39) missense probably damaging 1.00
R1603:Vmn2r91 UTSW 17 18,326,405 (GRCm39) missense probably benign 0.04
R1992:Vmn2r91 UTSW 17 18,356,142 (GRCm39) missense probably damaging 1.00
R2182:Vmn2r91 UTSW 17 18,325,691 (GRCm39) missense possibly damaging 0.94
R2424:Vmn2r91 UTSW 17 18,356,431 (GRCm39) nonsense probably null
R2512:Vmn2r91 UTSW 17 18,356,048 (GRCm39) missense probably benign
R2885:Vmn2r91 UTSW 17 18,325,628 (GRCm39) missense probably benign 0.00
R2909:Vmn2r91 UTSW 17 18,356,661 (GRCm39) missense probably damaging 1.00
R3009:Vmn2r91 UTSW 17 18,325,717 (GRCm39) missense probably benign 0.11
R3079:Vmn2r91 UTSW 17 18,355,973 (GRCm39) splice site probably null
R3080:Vmn2r91 UTSW 17 18,355,973 (GRCm39) splice site probably null
R3434:Vmn2r91 UTSW 17 18,330,370 (GRCm39) splice site probably benign
R3829:Vmn2r91 UTSW 17 18,325,759 (GRCm39) missense probably damaging 1.00
R3845:Vmn2r91 UTSW 17 18,327,860 (GRCm39) missense probably benign 0.00
R3846:Vmn2r91 UTSW 17 18,327,860 (GRCm39) missense probably benign 0.00
R4118:Vmn2r91 UTSW 17 18,330,358 (GRCm39) missense probably damaging 1.00
R4285:Vmn2r91 UTSW 17 18,356,030 (GRCm39) missense probably benign 0.00
R4729:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R4793:Vmn2r91 UTSW 17 18,325,658 (GRCm39) missense probably damaging 1.00
R4932:Vmn2r91 UTSW 17 18,356,751 (GRCm39) missense possibly damaging 0.84
R5016:Vmn2r91 UTSW 17 18,330,322 (GRCm39) nonsense probably null
R5018:Vmn2r91 UTSW 17 18,356,700 (GRCm39) missense probably damaging 1.00
R5605:Vmn2r91 UTSW 17 18,356,763 (GRCm39) missense probably damaging 1.00
R5815:Vmn2r91 UTSW 17 18,326,464 (GRCm39) missense probably benign 0.01
R6146:Vmn2r91 UTSW 17 18,356,518 (GRCm39) missense probably benign 0.07
R6187:Vmn2r91 UTSW 17 18,326,888 (GRCm39) missense probably benign 0.05
R6426:Vmn2r91 UTSW 17 18,355,865 (GRCm39) splice site probably null
R6450:Vmn2r91 UTSW 17 18,305,527 (GRCm39) missense probably damaging 0.98
R6767:Vmn2r91 UTSW 17 18,327,807 (GRCm39) missense probably damaging 0.98
R6986:Vmn2r91 UTSW 17 18,356,271 (GRCm39) missense probably benign 0.10
R7112:Vmn2r91 UTSW 17 18,325,880 (GRCm39) missense possibly damaging 0.83
R7178:Vmn2r91 UTSW 17 18,356,424 (GRCm39) missense probably damaging 1.00
R7330:Vmn2r91 UTSW 17 18,326,429 (GRCm39) missense probably damaging 1.00
R7368:Vmn2r91 UTSW 17 18,356,540 (GRCm39) missense possibly damaging 0.75
R7380:Vmn2r91 UTSW 17 18,356,838 (GRCm39) nonsense probably null
R7397:Vmn2r91 UTSW 17 18,356,060 (GRCm39) missense probably benign 0.02
R7625:Vmn2r91 UTSW 17 18,325,693 (GRCm39) missense probably damaging 1.00
R7739:Vmn2r91 UTSW 17 18,356,080 (GRCm39) missense probably benign 0.00
R7749:Vmn2r91 UTSW 17 18,356,540 (GRCm39) missense possibly damaging 0.75
R7755:Vmn2r91 UTSW 17 18,330,311 (GRCm39) missense possibly damaging 0.88
R7929:Vmn2r91 UTSW 17 18,327,906 (GRCm39) missense probably damaging 1.00
R7981:Vmn2r91 UTSW 17 18,327,887 (GRCm39) missense probably benign 0.02
R8211:Vmn2r91 UTSW 17 18,326,762 (GRCm39) missense probably damaging 1.00
R8325:Vmn2r91 UTSW 17 18,356,625 (GRCm39) missense probably damaging 1.00
R8781:Vmn2r91 UTSW 17 18,305,323 (GRCm39) missense possibly damaging 0.78
R8974:Vmn2r91 UTSW 17 18,325,636 (GRCm39) missense probably benign 0.27
R9047:Vmn2r91 UTSW 17 18,326,296 (GRCm39) missense probably benign 0.00
R9048:Vmn2r91 UTSW 17 18,356,122 (GRCm39) missense probably benign 0.00
R9109:Vmn2r91 UTSW 17 18,327,905 (GRCm39) missense probably damaging 1.00
R9211:Vmn2r91 UTSW 17 18,356,819 (GRCm39) nonsense probably null
R9555:Vmn2r91 UTSW 17 18,325,792 (GRCm39) missense possibly damaging 0.78
R9616:Vmn2r91 UTSW 17 18,356,305 (GRCm39) missense possibly damaging 0.81
Predicted Primers PCR Primer
(F):5'- ACCAAGCATACATGTACTGGAC -3'
(R):5'- GGTGAGTACCTCCAAATCACC -3'

Sequencing Primer
(F):5'- GGCTCTTGCAAGTTCCAAAATTTTTC -3'
(R):5'- ATTGCGGCATAATAAGAATAGCC -3'
Posted On 2015-03-18