Incidental Mutation 'IGL02659:Vmn2r77'
ID 302478
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r77
Ensembl Gene ENSMUSG00000090949
Gene Name vomeronasal 2, receptor 77
Synonyms EG546983
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # IGL02659
Quality Score
Status
Chromosome 7
Chromosomal Location 86444349-86461240 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 86449979 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Serine at position 75 (I75S)
Ref Sequence ENSEMBL: ENSMUSP00000129540 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164996]
AlphaFold L7N2B7
Predicted Effect probably benign
Transcript: ENSMUST00000164996
AA Change: I75S

PolyPhen 2 Score 0.320 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000129540
Gene: ENSMUSG00000090949
AA Change: I75S

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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr8 A T 14: 29,708,298 (GRCm39) N192I probably damaging Het
Arhgap15 A T 2: 43,953,849 (GRCm39) I192F probably damaging Het
Atp10a T C 7: 58,463,379 (GRCm39) F971L probably benign Het
Cacna1e G T 1: 154,302,274 (GRCm39) F1660L probably damaging Het
Cep152 G A 2: 125,421,469 (GRCm39) T1087M probably damaging Het
Ces2b T C 8: 105,559,202 (GRCm39) probably benign Het
Col19a1 T C 1: 24,573,115 (GRCm39) D219G unknown Het
Desi2 G A 1: 178,076,843 (GRCm39) A116T probably damaging Het
Eri2 T A 7: 119,386,665 (GRCm39) Q202L probably damaging Het
Gtf2ird1 G A 5: 134,405,895 (GRCm39) P715L probably damaging Het
Higd1c A T 15: 100,281,622 (GRCm39) M249L probably benign Het
Il5ra T A 6: 106,719,644 (GRCm39) H63L possibly damaging Het
Lamb3 T A 1: 193,014,469 (GRCm39) C543S probably damaging Het
Lnpep T A 17: 17,791,162 (GRCm39) I461F possibly damaging Het
Lum A G 10: 97,404,609 (GRCm39) H168R probably benign Het
Magi1 T C 6: 93,762,591 (GRCm39) E77G possibly damaging Het
Mrpl13 T C 15: 55,421,135 (GRCm39) probably null Het
Mtpap T A 18: 4,380,703 (GRCm39) L127* probably null Het
Myo15a T C 11: 60,382,609 (GRCm39) probably benign Het
Nek1 A G 8: 61,542,514 (GRCm39) S726G probably benign Het
Nlrp5 C A 7: 23,118,006 (GRCm39) H577N probably damaging Het
Nynrin G A 14: 56,103,554 (GRCm39) probably benign Het
Or14c40 A G 7: 86,313,289 (GRCm39) M140V probably benign Het
Or2h15 C T 17: 38,441,427 (GRCm39) G219S possibly damaging Het
Pappa2 A T 1: 158,764,364 (GRCm39) D382E probably damaging Het
Plekhg1 T A 10: 3,907,069 (GRCm39) L516* probably null Het
Prune1 A G 3: 95,162,711 (GRCm39) S321P possibly damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Syncrip G T 9: 88,338,457 (GRCm39) R536S probably benign Het
Thbs1 T G 2: 117,945,273 (GRCm39) V282G probably benign Het
Unc13b C T 4: 43,235,332 (GRCm39) R880C probably damaging Het
Vps13a A T 19: 16,630,063 (GRCm39) I2690K probably damaging Het
Zfp286 T C 11: 62,674,563 (GRCm39) N94S possibly damaging 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
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
R3037:Vmn2r77 UTSW 7 86,450,191 (GRCm39) missense probably benign
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
Posted On 2015-04-16