Incidental Mutation 'R3037:Vmn2r77'
ID 264852
Institutional Source Beutler Lab
Gene Symbol Vmn2r77
Ensembl Gene ENSMUSG00000090949
Gene Name vomeronasal 2, receptor 77
Synonyms EG546983
MMRRC Submission 040553-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # R3037 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 86444349-86461240 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 86450191 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 146 (I146L)
Ref Sequence ENSEMBL: ENSMUSP00000129540 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164996]
AlphaFold L7N2B7
Predicted Effect probably benign
Transcript: ENSMUST00000164996
AA Change: I146L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000129540
Gene: ENSMUSG00000090949
AA Change: I146L

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 78 467 1.4e-30 PFAM
Pfam:NCD3G 510 562 1e-20 PFAM
Pfam:7tm_3 594 830 2.6e-52 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap3b1 T C 13: 94,582,486 (GRCm39) probably null Het
Bco1 A G 8: 117,854,278 (GRCm39) Y401C probably benign Het
Bod1l A T 5: 41,979,380 (GRCm39) S645T probably damaging Het
Cat A G 2: 103,298,122 (GRCm39) Y274H probably benign Het
Cdh19 C A 1: 110,882,337 (GRCm39) V52F probably damaging Het
Cntnap2 G A 6: 45,992,200 (GRCm39) V376I possibly damaging Het
Dll3 A G 7: 27,998,542 (GRCm39) L141P probably damaging Het
Ets2 C A 16: 95,517,109 (GRCm39) N280K probably benign Het
Fam186a G T 15: 99,841,675 (GRCm39) P1523Q probably damaging Het
Fcgbp A G 7: 27,802,127 (GRCm39) I1352V possibly damaging Het
Fcsk A T 8: 111,621,350 (GRCm39) probably null Het
Gng11 A G 6: 4,008,051 (GRCm39) E38G probably benign Het
Gsdmc2 A T 15: 63,705,180 (GRCm39) F178I probably benign Het
Il11ra1 T A 4: 41,765,074 (GRCm39) S133R possibly damaging Het
Kcnab2 T A 4: 152,478,213 (GRCm39) I349F possibly damaging Het
Kctd10 A G 5: 114,513,061 (GRCm39) V38A probably damaging Het
Lrig3 A G 10: 125,845,901 (GRCm39) R777G probably damaging Het
Naip2 A C 13: 100,291,457 (GRCm39) D1160E probably benign Het
Nanog C A 6: 122,690,227 (GRCm39) Q186K possibly damaging Het
Nlrc3 T C 16: 3,770,272 (GRCm39) N249S probably damaging Het
Nup214 A T 2: 31,866,632 (GRCm39) T56S probably benign Het
Or8k41 A T 2: 86,313,987 (GRCm39) I33N probably damaging Het
Pcdhb1 T G 18: 37,398,166 (GRCm39) M39R probably damaging Het
Pced1a A C 2: 130,261,779 (GRCm39) D291E probably benign Het
Pdia6 C T 12: 17,329,646 (GRCm39) R261W probably damaging Het
Pdlim4 C A 11: 53,947,083 (GRCm39) G72V probably benign Het
Plce1 G A 19: 38,766,328 (GRCm39) D2104N probably damaging Het
Ptprk T C 10: 28,456,474 (GRCm39) L7P probably damaging Het
Rad21l A T 2: 151,502,700 (GRCm39) F170Y probably damaging Het
Scaf1 T C 7: 44,656,771 (GRCm39) probably benign Het
Topors C T 4: 40,269,673 (GRCm39) probably null Het
Trpm5 G A 7: 142,639,200 (GRCm39) T239I probably benign Het
Tspan5 G A 3: 138,604,116 (GRCm39) G167D probably damaging Het
Ttyh3 C A 5: 140,634,597 (GRCm39) probably benign Het
Usp15 C A 10: 122,999,522 (GRCm39) W220L probably damaging Het
Ythdf3 T C 3: 16,259,355 (GRCm39) F501L probably benign Het
Zc3h4 A G 7: 16,155,410 (GRCm39) D241G unknown Het
Other mutations in Vmn2r77
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00954:Vmn2r77 APN 7 86,449,975 (GRCm39) missense probably benign 0.06
IGL01105:Vmn2r77 APN 7 86,460,872 (GRCm39) missense probably damaging 0.99
IGL01367:Vmn2r77 APN 7 86,461,124 (GRCm39) missense probably damaging 0.98
IGL01634:Vmn2r77 APN 7 86,460,857 (GRCm39) missense probably benign
IGL01805:Vmn2r77 APN 7 86,460,395 (GRCm39) missense probably benign 0.18
IGL01868:Vmn2r77 APN 7 86,452,224 (GRCm39) missense probably benign 0.00
IGL01980:Vmn2r77 APN 7 86,450,678 (GRCm39) missense probably benign 0.14
IGL02055:Vmn2r77 APN 7 86,450,763 (GRCm39) missense probably benign 0.00
IGL02066:Vmn2r77 APN 7 86,452,836 (GRCm39) nonsense probably null
IGL02185:Vmn2r77 APN 7 86,444,360 (GRCm39) missense unknown
IGL02200:Vmn2r77 APN 7 86,451,187 (GRCm39) missense probably benign 0.04
IGL02336:Vmn2r77 APN 7 86,451,224 (GRCm39) missense probably damaging 0.99
IGL02445:Vmn2r77 APN 7 86,452,848 (GRCm39) nonsense probably null
IGL02557:Vmn2r77 APN 7 86,444,342 (GRCm39) unclassified probably benign
IGL02659:Vmn2r77 APN 7 86,449,979 (GRCm39) missense probably benign 0.32
IGL02978:Vmn2r77 APN 7 86,460,555 (GRCm39) missense probably benign
IGL03180:Vmn2r77 APN 7 86,450,843 (GRCm39) missense possibly damaging 0.85
IGL03255:Vmn2r77 APN 7 86,461,131 (GRCm39) missense probably benign 0.04
IGL03273:Vmn2r77 APN 7 86,460,494 (GRCm39) missense probably damaging 0.99
R0046:Vmn2r77 UTSW 7 86,451,146 (GRCm39) missense possibly damaging 0.73
R0047:Vmn2r77 UTSW 7 86,460,858 (GRCm39) missense probably benign 0.01
R0066:Vmn2r77 UTSW 7 86,449,964 (GRCm39) missense probably benign 0.17
R0066:Vmn2r77 UTSW 7 86,449,964 (GRCm39) missense probably benign 0.17
R0389:Vmn2r77 UTSW 7 86,450,702 (GRCm39) missense probably benign 0.29
R0635:Vmn2r77 UTSW 7 86,460,383 (GRCm39) missense probably benign
R0689:Vmn2r77 UTSW 7 86,460,872 (GRCm39) missense probably damaging 0.99
R0827:Vmn2r77 UTSW 7 86,451,224 (GRCm39) missense probably damaging 1.00
R1167:Vmn2r77 UTSW 7 86,450,954 (GRCm39) missense probably benign 0.02
R1228:Vmn2r77 UTSW 7 86,450,242 (GRCm39) critical splice donor site probably null
R1353:Vmn2r77 UTSW 7 86,451,394 (GRCm39) missense probably benign 0.29
R1392:Vmn2r77 UTSW 7 86,450,830 (GRCm39) missense probably benign 0.00
R1392:Vmn2r77 UTSW 7 86,450,830 (GRCm39) missense probably benign 0.00
R1613:Vmn2r77 UTSW 7 86,460,356 (GRCm39) missense probably damaging 1.00
R1654:Vmn2r77 UTSW 7 86,461,123 (GRCm39) missense probably damaging 1.00
R1742:Vmn2r77 UTSW 7 86,444,543 (GRCm39) missense probably benign 0.35
R1827:Vmn2r77 UTSW 7 86,450,821 (GRCm39) missense probably damaging 0.99
R1911:Vmn2r77 UTSW 7 86,461,001 (GRCm39) missense probably damaging 1.00
R1974:Vmn2r77 UTSW 7 86,449,964 (GRCm39) missense probably benign 0.17
R2008:Vmn2r77 UTSW 7 86,450,921 (GRCm39) missense probably benign 0.31
R2093:Vmn2r77 UTSW 7 86,450,702 (GRCm39) missense probably benign 0.29
R2143:Vmn2r77 UTSW 7 86,461,152 (GRCm39) missense probably damaging 1.00
R2269:Vmn2r77 UTSW 7 86,460,897 (GRCm39) missense probably benign 0.03
R2972:Vmn2r77 UTSW 7 86,452,893 (GRCm39) missense probably benign 0.01
R2974:Vmn2r77 UTSW 7 86,452,893 (GRCm39) missense probably benign 0.01
R3694:Vmn2r77 UTSW 7 86,450,044 (GRCm39) missense probably damaging 1.00
R3695:Vmn2r77 UTSW 7 86,450,044 (GRCm39) missense probably damaging 1.00
R3805:Vmn2r77 UTSW 7 86,444,368 (GRCm39) nonsense probably null
R3870:Vmn2r77 UTSW 7 86,461,050 (GRCm39) missense probably damaging 1.00
R4732:Vmn2r77 UTSW 7 86,450,195 (GRCm39) missense probably benign 0.00
R4733:Vmn2r77 UTSW 7 86,450,195 (GRCm39) missense probably benign 0.00
R5009:Vmn2r77 UTSW 7 86,451,015 (GRCm39) missense possibly damaging 0.82
R5201:Vmn2r77 UTSW 7 86,460,846 (GRCm39) missense probably damaging 0.98
R5218:Vmn2r77 UTSW 7 86,451,341 (GRCm39) missense probably damaging 0.98
R5469:Vmn2r77 UTSW 7 86,451,271 (GRCm39) missense probably benign 0.01
R5673:Vmn2r77 UTSW 7 86,461,214 (GRCm39) missense probably benign 0.05
R5771:Vmn2r77 UTSW 7 86,461,235 (GRCm39) missense probably benign 0.06
R5832:Vmn2r77 UTSW 7 86,460,670 (GRCm39) nonsense probably null
R5899:Vmn2r77 UTSW 7 86,460,924 (GRCm39) missense probably damaging 1.00
R6151:Vmn2r77 UTSW 7 86,450,878 (GRCm39) missense probably benign 0.00
R6182:Vmn2r77 UTSW 7 86,460,957 (GRCm39) missense probably damaging 1.00
R6326:Vmn2r77 UTSW 7 86,451,031 (GRCm39) missense probably benign
R6419:Vmn2r77 UTSW 7 86,460,767 (GRCm39) missense probably damaging 0.99
R6549:Vmn2r77 UTSW 7 86,450,065 (GRCm39) missense probably benign 0.06
R6874:Vmn2r77 UTSW 7 86,451,286 (GRCm39) missense probably benign 0.00
R6972:Vmn2r77 UTSW 7 86,452,202 (GRCm39) missense probably damaging 1.00
R7056:Vmn2r77 UTSW 7 86,451,023 (GRCm39) missense probably benign 0.06
R7185:Vmn2r77 UTSW 7 86,451,035 (GRCm39) missense probably benign 0.00
R7261:Vmn2r77 UTSW 7 86,460,518 (GRCm39) nonsense probably null
R7298:Vmn2r77 UTSW 7 86,449,979 (GRCm39) missense probably benign 0.00
R7662:Vmn2r77 UTSW 7 86,460,492 (GRCm39) nonsense probably null
R8182:Vmn2r77 UTSW 7 86,460,801 (GRCm39) missense probably damaging 1.00
R8327:Vmn2r77 UTSW 7 86,450,680 (GRCm39) missense probably benign 0.08
R8387:Vmn2r77 UTSW 7 86,450,947 (GRCm39) missense probably benign 0.00
R8825:Vmn2r77 UTSW 7 86,452,855 (GRCm39) missense probably benign
R8898:Vmn2r77 UTSW 7 86,444,430 (GRCm39) missense probably damaging 1.00
R8973:Vmn2r77 UTSW 7 86,452,150 (GRCm39) missense possibly damaging 0.93
R9258:Vmn2r77 UTSW 7 86,452,302 (GRCm39) missense possibly damaging 0.88
R9338:Vmn2r77 UTSW 7 86,460,994 (GRCm39) missense probably damaging 1.00
R9358:Vmn2r77 UTSW 7 86,452,236 (GRCm39) missense probably benign 0.00
R9377:Vmn2r77 UTSW 7 86,444,442 (GRCm39) missense probably benign 0.05
R9404:Vmn2r77 UTSW 7 86,451,247 (GRCm39) missense probably benign
R9673:Vmn2r77 UTSW 7 86,450,171 (GRCm39) missense possibly damaging 0.75
R9679:Vmn2r77 UTSW 7 86,460,741 (GRCm39) missense probably benign 0.07
Predicted Primers PCR Primer
(F):5'- AAGACCATCTACTTGATTTCCTCTG -3'
(R):5'- TCTCCTGCCCAACTGTCATAAAG -3'

Sequencing Primer
(F):5'- CCTCTGTTTATTTTGCCATTGAAG -3'
(R):5'- CCTGCCCAACTGTCATAAAGATGTTG -3'
Posted On 2015-02-05