Incidental Mutation 'IGL01511:Fbxw18'
ID89204
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fbxw18
Ensembl Gene ENSMUSG00000074059
Gene NameF-box and WD-40 domain protein 18
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.066) question?
Stock #IGL01511
Quality Score
Status
Chromosome9
Chromosomal Location109676734-109702700 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 109688821 bp
ZygosityHeterozygous
Amino Acid Change Serine to Threonine at position 366 (S366T)
Ref Sequence ENSEMBL: ENSMUSP00000095962 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098359]
Predicted Effect possibly damaging
Transcript: ENSMUST00000098359
AA Change: S366T

PolyPhen 2 Score 0.834 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000095962
Gene: ENSMUSG00000074059
AA Change: S366T

DomainStartEndE-ValueType
FBOX 8 48 4.13e-6 SMART
Blast:WD40 140 179 2e-7 BLAST
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca6 A T 11: 110,244,310 D216E probably benign Het
Abcc4 C A 14: 118,599,341 L669F probably benign Het
Adam29 C T 8: 55,871,421 G666D probably damaging Het
Adat2 T G 10: 13,560,238 M109R probably null Het
Atf3 T A 1: 191,171,496 T178S probably benign Het
Birc6 T A 17: 74,627,003 Y2522* probably null Het
Ccr8 G A 9: 120,094,625 G269R probably damaging Het
Ces1a G T 8: 93,045,098 P24T probably damaging Het
Chrna4 C T 2: 181,028,668 V432I probably benign Het
Commd8 A G 5: 72,165,379 V65A probably benign Het
Cyp2j13 A G 4: 96,077,315 F52L possibly damaging Het
Desi1 T A 15: 82,002,588 K45* probably null Het
Dmbt1 T A 7: 131,116,728 M1552K possibly damaging Het
Dna2 G A 10: 62,955,314 M197I possibly damaging Het
Dnah7a A C 1: 53,419,595 L3795V probably damaging Het
Fam221b T C 4: 43,660,135 probably null Het
Fzd8 A G 18: 9,213,293 Y125C unknown Het
Gcsam T C 16: 45,615,952 Y11H probably damaging Het
Gucy2f G T X: 142,161,734 D410E probably damaging Het
Hdac3 C T 18: 37,952,595 A53T probably benign Het
Lamp2 A G X: 38,431,875 L244P probably damaging Het
Lrrk1 A T 7: 66,265,450 F1630Y possibly damaging Het
M1ap C A 6: 83,028,412 D434E probably benign Het
Mcmbp A G 7: 128,707,164 Y378H probably damaging Het
Mvb12a T A 8: 71,545,302 V120E probably damaging Het
Nbeal2 A C 9: 110,629,234 W2063G probably damaging Het
Neto1 A C 18: 86,395,908 H9P possibly damaging Het
Nmu C T 5: 76,340,821 V126M probably damaging Het
Odf2 T C 2: 29,914,309 probably benign Het
Olfr1387 A G 11: 49,460,216 E179G probably damaging Het
Pdzrn3 T C 6: 101,153,256 H533R possibly damaging Het
Pikfyve G T 1: 65,258,869 E1586* probably null Het
Plcb3 C A 19: 6,955,843 R970L probably damaging Het
Plxna3 A G X: 74,335,308 E686G probably damaging Het
Polrmt T A 10: 79,740,151 Y586F probably benign Het
Ppt1 T A 4: 122,854,425 F225I probably damaging Het
Prcc T G 3: 87,872,241 D162A probably damaging Het
Ripor1 T C 8: 105,619,930 probably benign Het
Rnaseh1 A G 12: 28,659,009 H263R probably damaging Het
Rnf19b T A 4: 129,080,418 S490R probably damaging Het
Slc15a2 T A 16: 36,784,726 T23S probably damaging Het
Slc17a2 T C 13: 23,819,138 probably null Het
Slc35f4 T C 14: 49,298,877 M434V probably benign Het
Slc52a3 C T 2: 152,004,644 T175I probably benign Het
Slc5a2 C T 7: 128,270,622 T409M probably benign Het
Tbc1d24 A G 17: 24,181,918 S108P probably benign Het
Thnsl2 T G 6: 71,139,793 Q125P probably benign Het
Ttc13 T C 8: 124,676,371 D672G probably damaging Het
Ttn G T 2: 76,753,745 H14013N possibly damaging Het
Unc5a T C 13: 55,004,816 F792L probably damaging Het
Vac14 T C 8: 110,712,798 V669A possibly damaging Het
Vmn1r13 A T 6: 57,210,329 M158L probably benign Het
Vmn1r220 A T 13: 23,184,214 V104D probably damaging Het
Wdr78 T C 4: 103,048,361 D741G possibly damaging Het
Zfp738 A T 13: 67,683,401 probably null Het
Zscan5b A C 7: 6,231,422 H149P probably benign Het
Other mutations in Fbxw18
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Fbxw18 APN 9 109693343 missense probably benign 0.00
IGL00820:Fbxw18 APN 9 109693369 missense probably damaging 1.00
IGL01447:Fbxw18 APN 9 109701607 missense probably damaging 1.00
IGL01956:Fbxw18 APN 9 109693357 missense probably damaging 0.98
IGL02089:Fbxw18 APN 9 109701322 missense probably benign 0.00
PIT4810001:Fbxw18 UTSW 9 109676890 nonsense probably null
R0004:Fbxw18 UTSW 9 109701313 missense probably damaging 0.96
R0124:Fbxw18 UTSW 9 109691515 missense probably benign 0.00
R0375:Fbxw18 UTSW 9 109688839 missense possibly damaging 0.63
R1652:Fbxw18 UTSW 9 109690627 missense probably benign 0.35
R2153:Fbxw18 UTSW 9 109693370 missense probably damaging 1.00
R2294:Fbxw18 UTSW 9 109676797 missense probably damaging 1.00
R3738:Fbxw18 UTSW 9 109688913 missense possibly damaging 0.57
R4706:Fbxw18 UTSW 9 109690517 missense probably benign 0.00
R4982:Fbxw18 UTSW 9 109702651 start gained probably benign
R4990:Fbxw18 UTSW 9 109688393 missense probably damaging 0.99
R5314:Fbxw18 UTSW 9 109693178 missense possibly damaging 0.90
R5520:Fbxw18 UTSW 9 109691521 missense probably benign 0.00
R5634:Fbxw18 UTSW 9 109676803 missense possibly damaging 0.49
R5718:Fbxw18 UTSW 9 109691568 missense probably benign 0.01
R5894:Fbxw18 UTSW 9 109700167 missense possibly damaging 0.83
R5928:Fbxw18 UTSW 9 109700081 missense probably damaging 0.99
R6175:Fbxw18 UTSW 9 109676879 missense probably damaging 1.00
R6696:Fbxw18 UTSW 9 109688764 missense probably benign 0.09
R6944:Fbxw18 UTSW 9 109702587 missense probably damaging 1.00
R7396:Fbxw18 UTSW 9 109688886 missense probably benign 0.19
Posted On2013-12-03