Incidental Mutation 'R1323:Vmn2r114'
ID 157746
Institutional Source Beutler Lab
Gene Symbol Vmn2r114
Ensembl Gene ENSMUSG00000091945
Gene Name vomeronasal 2, receptor 114
Synonyms EG666002
MMRRC Submission 039389-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.131) question?
Stock # R1323 (G1)
Quality Score 111
Status Not validated
Chromosome 17
Chromosomal Location 23509908-23531287 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) ATTT to ATT at 23509906 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127505 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168033]
AlphaFold E9Q281
Predicted Effect probably null
Transcript: ENSMUST00000168033
SMART Domains Protein: ENSMUSP00000127505
Gene: ENSMUSG00000091945

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 154 470 1.5e-24 PFAM
Pfam:NCD3G 511 564 1.5e-18 PFAM
Pfam:7tm_3 597 832 1.4e-55 PFAM
Coding Region Coverage
  • 1x: 98.3%
  • 3x: 96.6%
  • 10x: 89.2%
  • 20x: 70.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 C A 11: 9,240,937 (GRCm39) F933L possibly damaging Het
Abcc8 T G 7: 45,766,786 (GRCm39) Q998P probably benign Het
Akr1e1 C T 13: 4,657,547 (GRCm39) G17E probably damaging Het
D630045J12Rik T C 6: 38,125,443 (GRCm39) I1524V probably damaging Het
Elovl1 T C 4: 118,288,851 (GRCm39) L103P possibly damaging Het
Fam171a2 T G 11: 102,334,951 (GRCm39) D62A probably damaging Het
Frzb G A 2: 80,243,720 (GRCm39) P320S probably benign Het
Fsip2 G T 2: 82,816,096 (GRCm39) G3943V probably damaging Het
Ftdc1 G A 16: 58,437,278 (GRCm39) P10L possibly damaging Het
Grm8 A G 6: 28,125,973 (GRCm39) L51P probably damaging Het
H2af-ps2 T G 13: 51,357,100 (GRCm39) noncoding transcript Het
Hnf4g T C 3: 3,699,281 (GRCm39) S4P possibly damaging Het
Megf8 T A 7: 25,059,527 (GRCm39) probably null Het
Mtnr1b A G 9: 15,774,432 (GRCm39) F209S probably damaging Het
Nckipsd G A 9: 108,689,778 (GRCm39) R313Q probably damaging Het
Nrbp1 T A 5: 31,403,157 (GRCm39) I210N probably damaging Het
Paqr5 C T 9: 61,868,810 (GRCm39) probably null Het
S100a14 T C 3: 90,435,043 (GRCm39) V18A probably damaging Het
Sycp2 A T 2: 177,989,414 (GRCm39) S1441R possibly damaging Het
Vmn2r101 G A 17: 19,832,313 (GRCm39) D770N probably damaging Het
Zfp600 A G 4: 146,133,261 (GRCm39) Y643C probably damaging Het
Other mutations in Vmn2r114
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00157:Vmn2r114 APN 17 23,510,639 (GRCm39) missense probably damaging 1.00
IGL00990:Vmn2r114 APN 17 23,510,212 (GRCm39) missense probably damaging 1.00
IGL00990:Vmn2r114 APN 17 23,509,957 (GRCm39) missense probably benign 0.23
IGL00990:Vmn2r114 APN 17 23,509,939 (GRCm39) missense probably benign
IGL01838:Vmn2r114 APN 17 23,515,956 (GRCm39) missense probably benign 0.44
IGL01990:Vmn2r114 APN 17 23,529,355 (GRCm39) missense probably benign 0.22
IGL01994:Vmn2r114 APN 17 23,529,451 (GRCm39) missense probably damaging 1.00
IGL02153:Vmn2r114 APN 17 23,510,782 (GRCm39) missense probably benign 0.01
IGL02453:Vmn2r114 APN 17 23,530,108 (GRCm39) missense probably benign 0.00
IGL02621:Vmn2r114 APN 17 23,529,494 (GRCm39) missense probably damaging 0.98
IGL02938:Vmn2r114 APN 17 23,510,263 (GRCm39) missense probably benign 0.10
IGL03130:Vmn2r114 APN 17 23,515,970 (GRCm39) splice site probably benign
IGL03325:Vmn2r114 APN 17 23,510,652 (GRCm39) missense probably damaging 1.00
BB004:Vmn2r114 UTSW 17 23,510,619 (GRCm39) missense probably damaging 1.00
R0109:Vmn2r114 UTSW 17 23,529,549 (GRCm39) nonsense probably null
R0164:Vmn2r114 UTSW 17 23,528,800 (GRCm39) critical splice donor site probably null
R0310:Vmn2r114 UTSW 17 23,509,917 (GRCm39) missense probably benign 0.23
R0583:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R0677:Vmn2r114 UTSW 17 23,529,568 (GRCm39) missense probably damaging 1.00
R1127:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R1147:Vmn2r114 UTSW 17 23,530,037 (GRCm39) missense probably benign 0.00
R1147:Vmn2r114 UTSW 17 23,530,037 (GRCm39) missense probably benign 0.00
R1157:Vmn2r114 UTSW 17 23,529,314 (GRCm39) missense possibly damaging 0.60
R1347:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R1435:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R1437:Vmn2r114 UTSW 17 23,510,185 (GRCm39) missense probably damaging 1.00
R1585:Vmn2r114 UTSW 17 23,510,675 (GRCm39) missense probably damaging 0.98
R1641:Vmn2r114 UTSW 17 23,515,962 (GRCm39) missense probably benign 0.00
R1748:Vmn2r114 UTSW 17 23,527,035 (GRCm39) missense probably benign 0.17
R1954:Vmn2r114 UTSW 17 23,530,086 (GRCm39) missense probably benign 0.32
R2081:Vmn2r114 UTSW 17 23,510,083 (GRCm39) missense possibly damaging 0.91
R2103:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R2113:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R2134:Vmn2r114 UTSW 17 23,510,737 (GRCm39) missense probably damaging 1.00
R2149:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R2424:Vmn2r114 UTSW 17 23,515,842 (GRCm39) missense possibly damaging 0.90
R2847:Vmn2r114 UTSW 17 23,509,948 (GRCm39) missense probably benign 0.00
R2848:Vmn2r114 UTSW 17 23,509,948 (GRCm39) missense probably benign 0.00
R2893:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R3017:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R3018:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R3019:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R3020:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R3021:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R4628:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R4668:Vmn2r114 UTSW 17 23,529,447 (GRCm39) missense possibly damaging 0.83
R4840:Vmn2r114 UTSW 17 23,510,353 (GRCm39) missense probably damaging 0.97
R4841:Vmn2r114 UTSW 17 23,529,336 (GRCm39) missense probably benign 0.04
R4842:Vmn2r114 UTSW 17 23,529,336 (GRCm39) missense probably benign 0.04
R4856:Vmn2r114 UTSW 17 23,527,008 (GRCm39) missense probably benign 0.11
R4886:Vmn2r114 UTSW 17 23,527,008 (GRCm39) missense probably benign 0.11
R4992:Vmn2r114 UTSW 17 23,510,765 (GRCm39) missense probably benign 0.03
R5182:Vmn2r114 UTSW 17 23,510,632 (GRCm39) missense probably damaging 0.96
R5223:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R5405:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R5449:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R5615:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
R5834:Vmn2r114 UTSW 17 23,529,599 (GRCm39) missense possibly damaging 0.90
R6150:Vmn2r114 UTSW 17 23,510,269 (GRCm39) missense probably benign 0.03
R6277:Vmn2r114 UTSW 17 23,509,954 (GRCm39) missense possibly damaging 0.93
R6403:Vmn2r114 UTSW 17 23,528,939 (GRCm39) missense probably damaging 0.99
R6589:Vmn2r114 UTSW 17 23,510,642 (GRCm39) missense probably damaging 1.00
R6613:Vmn2r114 UTSW 17 23,529,220 (GRCm39) missense possibly damaging 0.82
R6747:Vmn2r114 UTSW 17 23,528,850 (GRCm39) missense probably benign 0.00
R6837:Vmn2r114 UTSW 17 23,529,176 (GRCm39) missense probably benign 0.10
R6911:Vmn2r114 UTSW 17 23,510,104 (GRCm39) missense probably damaging 0.98
R6950:Vmn2r114 UTSW 17 23,529,137 (GRCm39) missense probably benign 0.03
R7276:Vmn2r114 UTSW 17 23,509,934 (GRCm39) missense probably damaging 0.97
R7482:Vmn2r114 UTSW 17 23,510,468 (GRCm39) missense probably damaging 1.00
R7514:Vmn2r114 UTSW 17 23,527,035 (GRCm39) missense probably null 0.96
R7523:Vmn2r114 UTSW 17 23,529,611 (GRCm39) missense probably benign 0.01
R7563:Vmn2r114 UTSW 17 23,510,000 (GRCm39) missense probably benign 0.01
R7585:Vmn2r114 UTSW 17 23,510,239 (GRCm39) missense probably damaging 1.00
R7593:Vmn2r114 UTSW 17 23,510,817 (GRCm39) nonsense probably null
R7611:Vmn2r114 UTSW 17 23,515,944 (GRCm39) missense probably damaging 0.97
R7641:Vmn2r114 UTSW 17 23,527,177 (GRCm39) missense possibly damaging 0.53
R7651:Vmn2r114 UTSW 17 23,509,986 (GRCm39) nonsense probably null
R7970:Vmn2r114 UTSW 17 23,530,186 (GRCm39) missense probably benign 0.00
R8737:Vmn2r114 UTSW 17 23,529,142 (GRCm39) missense probably benign 0.36
R8802:Vmn2r114 UTSW 17 23,528,836 (GRCm39) missense possibly damaging 0.65
R8847:Vmn2r114 UTSW 17 23,528,986 (GRCm39) missense probably damaging 1.00
R8991:Vmn2r114 UTSW 17 23,529,286 (GRCm39) missense probably damaging 1.00
R9138:Vmn2r114 UTSW 17 23,510,578 (GRCm39) missense probably damaging 1.00
R9173:Vmn2r114 UTSW 17 23,510,527 (GRCm39) missense probably damaging 0.99
R9175:Vmn2r114 UTSW 17 23,527,212 (GRCm39) missense probably damaging 1.00
R9657:Vmn2r114 UTSW 17 23,510,690 (GRCm39) missense probably damaging 1.00
R9670:Vmn2r114 UTSW 17 23,531,098 (GRCm39) missense
X0065:Vmn2r114 UTSW 17 23,529,931 (GRCm39) missense probably benign 0.34
Z1088:Vmn2r114 UTSW 17 23,509,906 (GRCm39) makesense probably null
Predicted Primers PCR Primer
(F):5'- ACGAGAATATTGAAAAGCAGACTCCCAG -3'
(R):5'- TGTTTACCATAGCACCAAAGGCAGG -3'

Sequencing Primer
(F):5'- gcaacccaaaaaagagcatctg -3'
(R):5'- CAAAGGCAGGGTCATGGTG -3'
Posted On 2014-02-18