Incidental Mutation 'R5236:Fbxw9'
ID 398399
Institutional Source Beutler Lab
Gene Symbol Fbxw9
Ensembl Gene ENSMUSG00000008167
Gene Name F-box and WD-40 domain protein 9
Synonyms Fbw9, 1110017H11Rik
MMRRC Submission 044393-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # R5236 (G1)
Quality Score 225
Status Not validated
Chromosome 8
Chromosomal Location 85786748-85793750 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 85792974 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 407 (T407A)
Ref Sequence ENSEMBL: ENSMUSP00000092845 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095220] [ENSMUST00000177563]
AlphaFold F8VPX2
Predicted Effect probably damaging
Transcript: ENSMUST00000095220
AA Change: T407A

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000092845
Gene: ENSMUSG00000008167
AA Change: T407A

DomainStartEndE-ValueType
low complexity region 15 27 N/A INTRINSIC
FBOX 82 123 7.47e-4 SMART
WD40 161 201 2.98e-1 SMART
WD40 210 252 4.55e-3 SMART
WD40 256 292 7.8e-2 SMART
WD40 296 333 1.03e0 SMART
WD40 377 415 2.57e0 SMART
Blast:WD40 419 455 8e-17 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125109
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139721
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141183
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142036
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143763
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145479
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151962
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211210
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183657
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152884
Predicted Effect probably benign
Transcript: ENSMUST00000177563
SMART Domains Protein: ENSMUSP00000136655
Gene: ENSMUSG00000095845

DomainStartEndE-ValueType
G_gamma 7 72 2.19e-22 SMART
GGL 11 72 6.32e-27 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.3%
  • 20x: 92.4%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the F-box protein family, such as FBXW9, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9630041A04Rik T A 9: 101,820,120 (GRCm39) I180N possibly damaging Het
Actl9 T C 17: 33,653,073 (GRCm39) S378P probably damaging Het
Agrn A T 4: 156,263,315 (GRCm39) C263S possibly damaging Het
Ahnak A G 19: 8,978,048 (GRCm39) I56V possibly damaging Het
Arid4b A G 13: 14,301,034 (GRCm39) probably null Het
Bin2 T C 15: 100,560,415 (GRCm39) N49D probably damaging Het
Ccdc39 T C 3: 33,884,251 (GRCm39) T364A probably damaging Het
Cdcp1 A T 9: 123,014,258 (GRCm39) V172D probably damaging Het
Cdh23 A G 10: 60,148,351 (GRCm39) L2670P probably damaging Het
Cmtm4 G C 8: 105,084,378 (GRCm39) F105L probably damaging Het
Cspg4b A G 13: 113,502,754 (GRCm39) Y153C probably benign Het
Ctsa G A 2: 164,680,831 (GRCm39) V453M probably damaging Het
Cyp3a59 A G 5: 146,039,635 (GRCm39) I303V probably benign Het
Cyp4f17 T C 17: 32,739,606 (GRCm39) probably null Het
Dst C T 1: 34,203,498 (GRCm39) R447C probably damaging Het
E2f7 C T 10: 110,603,070 (GRCm39) P362S probably damaging Het
Fyb2 T C 4: 104,805,957 (GRCm39) S346P probably benign Het
Git2 T A 5: 114,905,233 (GRCm39) I75L probably damaging Het
H2-DMa T A 17: 34,356,913 (GRCm39) L137Q probably damaging Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Hrg T C 16: 22,780,263 (GRCm39) probably benign Het
Htr7 A T 19: 36,034,169 (GRCm39) I162N probably damaging Het
Itpripl1 A T 2: 126,983,770 (GRCm39) F117L probably damaging Het
Kri1 T C 9: 21,187,237 (GRCm39) Y392C probably damaging Het
Krt27 A C 11: 99,241,641 (GRCm39) S87A possibly damaging Het
Lama1 T C 17: 68,111,487 (GRCm39) V2246A probably benign Het
Lcn2 A T 2: 32,275,973 (GRCm39) M119K probably benign Het
Lrp2 T C 2: 69,287,163 (GRCm39) probably null Het
Lrp6 T C 6: 134,488,227 (GRCm39) N290D probably damaging Het
Macf1 T C 4: 123,291,614 (GRCm39) E2517G probably damaging Het
Melk G A 4: 44,344,959 (GRCm39) C363Y probably benign Het
Mettl22 T A 16: 8,306,597 (GRCm39) L351* probably null Het
Mms22l A G 4: 24,588,347 (GRCm39) Q953R probably benign Het
Ndufaf7 T C 17: 79,247,060 (GRCm39) S107P probably benign Het
Opa3 A G 7: 18,978,682 (GRCm39) Y49C probably damaging Het
Or2a12 A C 6: 42,904,715 (GRCm39) R183S probably benign Het
Or9a2 C A 6: 41,749,045 (GRCm39) G63C probably benign Het
Pabpn1 T A 14: 55,132,399 (GRCm39) M145K possibly damaging Het
Plce1 A C 19: 38,758,791 (GRCm39) M1982L probably benign Het
Ppcdc A C 9: 57,321,937 (GRCm39) I201S probably benign Het
Rag2 A T 2: 101,460,005 (GRCm39) D105V probably damaging Het
Rnf130 C T 11: 49,986,805 (GRCm39) T383I probably damaging Het
Sgip1 T G 4: 102,784,784 (GRCm39) probably null Het
Slc23a2 T A 2: 131,917,504 (GRCm39) I245F probably damaging Het
Slc4a9 A G 18: 36,663,900 (GRCm39) Y308C probably benign Het
Slc7a15 C T 12: 8,589,005 (GRCm39) V181M probably benign Het
Sprr2b G A 3: 92,224,943 (GRCm39) C63Y unknown Het
Stpg2 A T 3: 138,937,984 (GRCm39) Y181F probably damaging Het
Sult2a5 A T 7: 13,398,974 (GRCm39) T194S probably benign Het
Tbx15 A T 3: 99,259,362 (GRCm39) Q411L possibly damaging Het
Tln2 T A 9: 67,273,205 (GRCm39) E427V probably damaging Het
Trpv4 A C 5: 114,760,856 (GRCm39) V825G possibly damaging Het
Trrap A G 5: 144,754,596 (GRCm39) I1968V probably benign Het
Ttn G A 2: 76,619,146 (GRCm39) L16078F probably damaging Het
Unc45b T A 11: 82,805,888 (GRCm39) F132I possibly damaging Het
Unc79 T A 12: 103,060,654 (GRCm39) probably null Het
Vmn2r71 A T 7: 85,272,877 (GRCm39) N564Y probably damaging Het
Zfp638 G T 6: 83,953,557 (GRCm39) E1221* probably null Het
Zfp934 A T 13: 62,665,527 (GRCm39) H371Q probably damaging Het
Zranb3 A G 1: 127,968,726 (GRCm39) L63P probably damaging Het
Other mutations in Fbxw9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00541:Fbxw9 APN 8 85,793,219 (GRCm39) missense probably damaging 0.99
IGL01108:Fbxw9 APN 8 85,792,606 (GRCm39) unclassified probably benign
IGL01633:Fbxw9 APN 8 85,791,055 (GRCm39) missense probably damaging 1.00
IGL02672:Fbxw9 APN 8 85,792,682 (GRCm39) splice site probably null
R0053:Fbxw9 UTSW 8 85,791,083 (GRCm39) missense probably damaging 1.00
R0053:Fbxw9 UTSW 8 85,791,083 (GRCm39) missense probably damaging 1.00
R0535:Fbxw9 UTSW 8 85,791,229 (GRCm39) missense probably damaging 1.00
R0961:Fbxw9 UTSW 8 85,788,658 (GRCm39) missense probably benign 0.05
R1171:Fbxw9 UTSW 8 85,792,707 (GRCm39) missense possibly damaging 0.95
R2371:Fbxw9 UTSW 8 85,788,658 (GRCm39) missense probably benign 0.05
R4472:Fbxw9 UTSW 8 85,786,829 (GRCm39) missense probably damaging 1.00
R4864:Fbxw9 UTSW 8 85,792,530 (GRCm39) missense probably damaging 1.00
R4865:Fbxw9 UTSW 8 85,786,785 (GRCm39) missense possibly damaging 0.62
R5771:Fbxw9 UTSW 8 85,791,201 (GRCm39) splice site probably null
R6670:Fbxw9 UTSW 8 85,788,839 (GRCm39) missense possibly damaging 0.55
R6861:Fbxw9 UTSW 8 85,792,740 (GRCm39) missense probably damaging 0.99
R7354:Fbxw9 UTSW 8 85,788,825 (GRCm39) missense probably damaging 1.00
R9222:Fbxw9 UTSW 8 85,788,856 (GRCm39) missense probably damaging 0.99
R9776:Fbxw9 UTSW 8 85,792,523 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- ATCGAGATGGTTGCTTCCAG -3'
(R):5'- GCCAGCAGGTTATATGAGGCAG -3'

Sequencing Primer
(F):5'- GTTCGGGTCTGCTAGGATCCC -3'
(R):5'- GGACCTTACCCCATTTAACACGTTG -3'
Posted On 2016-07-06