Incidental Mutation 'IGL02105:Vmn1r76'
ID279924
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r76
Ensembl Gene ENSMUSG00000115267
Gene Namevomeronasal 1 receptor 76
SynonymsV1rg4
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.199) question?
Stock #IGL02105
Quality Score
Status
Chromosome7
Chromosomal Location11923523-11938213 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 11930490 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 266 (S266P)
Ref Sequence ENSEMBL: ENSMUSP00000055518 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058772] [ENSMUST00000226300] [ENSMUST00000226947]
Predicted Effect possibly damaging
Transcript: ENSMUST00000058772
AA Change: S266P

PolyPhen 2 Score 0.458 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000055518
Gene: ENSMUSG00000115267
AA Change: S266P

DomainStartEndE-ValueType
transmembrane domain 5 27 N/A INTRINSIC
transmembrane domain 31 53 N/A INTRINSIC
Pfam:V1R 54 317 5.4e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226300
AA Change: S231P

PolyPhen 2 Score 0.191 (Sensitivity: 0.92; Specificity: 0.87)
Predicted Effect probably benign
Transcript: ENSMUST00000226947
AA Change: S231P

PolyPhen 2 Score 0.191 (Sensitivity: 0.92; Specificity: 0.87)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl4 G T 3: 95,680,064 P734H probably damaging Het
Arfip2 A T 7: 105,639,383 I14N probably damaging Het
Asap3 G T 4: 136,228,474 probably null Het
Atg2a T A 19: 6,250,403 probably benign Het
Bbs12 T C 3: 37,320,147 L248P probably damaging Het
Brd3 A T 2: 27,459,776 I255N probably damaging Het
Ccdc141 A G 2: 77,049,577 probably null Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Chd9 T A 8: 90,932,488 D25E probably damaging Het
Cobl T C 11: 12,249,651 K1325R probably damaging Het
Dnmt1 T A 9: 20,907,882 E1486V unknown Het
Dock2 T C 11: 34,714,525 N256D probably damaging Het
Dpp3 G A 19: 4,916,771 S408L probably damaging Het
Dync2h1 C T 9: 7,075,892 G2992R probably damaging Het
Eef1a1 T C 9: 78,480,551 D35G probably benign Het
Fntb A G 12: 76,862,489 K84E probably benign Het
Gfi1 A G 5: 107,723,722 probably null Het
Glb1l3 T A 9: 26,818,527 I516F probably damaging Het
Hltf A G 3: 20,092,757 N560S probably damaging Het
Kif21b A G 1: 136,171,303 N1443S probably benign Het
Knl1 T A 2: 119,071,808 I1330K probably benign Het
Krt20 C T 11: 99,438,001 V33M probably benign Het
Lao1 A G 4: 118,968,443 T487A probably damaging Het
Larp4 A G 15: 99,986,071 E63G probably damaging Het
Lrp1 A G 10: 127,544,579 V3901A probably damaging Het
Lrrc17 A G 5: 21,570,257 I272M probably benign Het
Malrd1 A T 2: 16,127,863 Q1865L unknown Het
Mtg1 T C 7: 140,150,206 L305P probably damaging Het
Mylk4 T A 13: 32,720,562 E427D probably benign Het
Myom1 G T 17: 71,047,716 probably benign Het
Nbeal1 A G 1: 60,253,501 E1104G probably damaging Het
Obox5 A G 7: 15,758,575 M152V probably benign Het
Olfm2 C T 9: 20,672,180 V203M probably damaging Het
Olfr166 T G 16: 19,487,261 L141R probably benign Het
Olfr876 A T 9: 37,804,595 H228L possibly damaging Het
Pf4 A G 5: 90,773,255 S105G probably damaging Het
Phlpp2 T A 8: 109,904,408 I228N probably damaging Het
Sall1 T G 8: 89,032,568 S303R probably damaging Het
Setd5 A G 6: 113,117,580 E486G probably damaging Het
Slc9a5 C T 8: 105,349,443 P23S probably damaging Het
Tbc1d9b T A 11: 50,149,826 I390N probably damaging Het
Trp53 T C 11: 69,588,503 V169A probably damaging Het
Usp4 A G 9: 108,384,932 D791G probably damaging Het
Vmn2r27 A G 6: 124,197,349 probably benign Het
Xirp1 C T 9: 120,016,997 G940E probably damaging Het
Zfp407 A T 18: 84,562,720 C89* probably null Het
Other mutations in Vmn1r76
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01017:Vmn1r76 APN 7 11930382 missense possibly damaging 0.50
IGL01353:Vmn1r76 APN 7 11930810 missense probably damaging 0.98
R0032:Vmn1r76 UTSW 7 11931267 missense probably benign
R0879:Vmn1r76 UTSW 7 11930735 missense probably benign 0.00
R1201:Vmn1r76 UTSW 7 11930325 missense probably benign 0.38
R1966:Vmn1r76 UTSW 7 11930514 missense probably damaging 1.00
R3030:Vmn1r76 UTSW 7 11930475 missense probably damaging 1.00
R3915:Vmn1r76 UTSW 7 11930569 missense probably benign 0.23
R4295:Vmn1r76 UTSW 7 11931130 missense probably benign 0.44
R5053:Vmn1r76 UTSW 7 11930314 synonymous probably null
R5450:Vmn1r76 UTSW 7 11930684 missense probably damaging 1.00
R5568:Vmn1r76 UTSW 7 11931135 missense probably benign 0.02
R6382:Vmn1r76 UTSW 7 11930499 missense probably damaging 1.00
R7137:Vmn1r76 UTSW 7 11930685 missense possibly damaging 0.94
R7704:Vmn1r76 UTSW 7 11930417 missense probably benign 0.25
R8018:Vmn1r76 UTSW 7 11930883 missense not run
Z1176:Vmn1r76 UTSW 7 11930568 missense not run
Posted On2015-04-16