Incidental Mutation 'R8385:Fbxo22'
ID 647125
Institutional Source Beutler Lab
Gene Symbol Fbxo22
Ensembl Gene ENSMUSG00000032309
Gene Name F-box protein 22
Synonyms 0610033L19Rik, 1600016C16Rik
MMRRC Submission 067751-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8385 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 55116219-55131717 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 55121233 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 106 (D106G)
Ref Sequence ENSEMBL: ENSMUSP00000034859 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034859] [ENSMUST00000133795] [ENSMUST00000140375] [ENSMUST00000146201] [ENSMUST00000153970]
AlphaFold Q78JE5
Predicted Effect probably damaging
Transcript: ENSMUST00000034859
AA Change: D106G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000034859
Gene: ENSMUSG00000032309
AA Change: D106G

DomainStartEndE-ValueType
Pfam:F-box 22 66 1.7e-6 PFAM
FIST_C 231 365 2.61e-6 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000133795
AA Change: D3G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Predicted Effect probably damaging
Transcript: ENSMUST00000140375
AA Change: D106G

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000117341
Gene: ENSMUSG00000032309
AA Change: D106G

DomainStartEndE-ValueType
Pfam:F-box 21 66 3e-8 PFAM
Pfam:F-box-like 26 66 4.5e-8 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000146201
AA Change: D3G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000117106
Gene: ENSMUSG00000032309
AA Change: D3G

DomainStartEndE-ValueType
FIST_C 128 262 2.61e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000153970
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and, as a transcriptional target of the tumor protein p53, is thought to be involved in degradation of specific proteins in response to p53 induction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Brap C T 5: 121,823,197 (GRCm39) T473I probably benign Het
Cacna1e T A 1: 154,319,687 (GRCm39) M1400L probably damaging Het
Catsper2 A G 2: 121,240,621 (GRCm39) I127T possibly damaging Het
Dbt A T 3: 116,317,039 (GRCm39) I72F probably damaging Het
Ddhd2 T C 8: 26,225,041 (GRCm39) H592R probably damaging Het
Disp2 T A 2: 118,620,891 (GRCm39) M541K probably damaging Het
Dnai7 C T 6: 145,120,918 (GRCm39) E685K probably damaging Het
Dnmbp T C 19: 43,878,090 (GRCm39) D327G probably benign Het
Dvl1 A G 4: 155,940,037 (GRCm39) S390G possibly damaging Het
Gfm2 A G 13: 97,301,519 (GRCm39) T441A probably benign Het
Gm5431 T C 11: 48,780,347 (GRCm39) I192V probably damaging Het
Gosr1 T A 11: 76,620,967 (GRCm39) T241S possibly damaging Het
Hk2 T C 6: 82,706,527 (GRCm39) S792G probably benign Het
Itsn1 A C 16: 91,690,699 (GRCm39) K1302Q unknown Het
Kif16b T C 2: 142,554,258 (GRCm39) K847E probably benign Het
Lfng G A 5: 140,598,981 (GRCm39) E297K probably damaging Het
Mark3 A G 12: 111,621,808 (GRCm39) D650G possibly damaging Het
Mgat4f A G 1: 134,318,376 (GRCm39) K383E probably benign Het
Mob3b T C 4: 34,985,980 (GRCm39) Y186C probably damaging Het
Mphosph9 T C 5: 124,450,785 (GRCm39) K329E probably benign Het
Mta1 A T 12: 113,095,085 (GRCm39) M448L probably benign Het
Mterf1a A T 5: 3,941,384 (GRCm39) N161K probably damaging Het
Myo10 T A 15: 25,804,484 (GRCm39) I1593N probably damaging Het
Naca A G 10: 127,878,307 (GRCm39) N1113S unknown Het
Or2w4 T C 13: 21,795,522 (GRCm39) I206V probably benign Het
Or5e1 T G 7: 108,354,511 (GRCm39) Y149* probably null Het
Pcdhga1 A T 18: 37,795,149 (GRCm39) D51V probably damaging Het
Peg3 T C 7: 6,711,082 (GRCm39) E1380G probably damaging Het
Pkd1 G A 17: 24,794,702 (GRCm39) V2130M possibly damaging Het
Pla2g4c C T 7: 13,063,589 (GRCm39) P19S probably benign Het
Popdc2 G A 16: 38,183,262 (GRCm39) V82I probably benign Het
Ppfibp2 A G 7: 107,296,894 (GRCm39) R203G probably benign Het
Rab19 T A 6: 39,360,892 (GRCm39) N13K probably benign Het
Raet1d T A 10: 22,246,817 (GRCm39) D48E probably benign Het
Rell1 T A 5: 64,087,861 (GRCm39) K136* probably null Het
Slc38a4 A G 15: 96,897,393 (GRCm39) I474T probably damaging Het
Slf1 T C 13: 77,254,109 (GRCm39) M243V probably benign Het
Spata31f1a C T 4: 42,850,509 (GRCm39) R549H possibly damaging Het
Speer4c2 A T 5: 15,857,669 (GRCm39) S203T unknown Het
Spg11 A T 2: 121,927,802 (GRCm39) S661T probably benign Het
Thra C G 11: 98,659,177 (GRCm39) S435R probably benign Het
Tmem181a T C 17: 6,339,274 (GRCm39) I61T probably benign Het
Ttpa G A 4: 20,028,483 (GRCm39) G247S probably damaging Het
Usp17lb C T 7: 104,489,830 (GRCm39) V366I possibly damaging Het
Vit A T 17: 78,927,066 (GRCm39) Q337L probably benign Het
Vmn2r102 A G 17: 19,914,088 (GRCm39) Y551C possibly damaging Het
Vps52 T C 17: 34,181,791 (GRCm39) L539P probably damaging Het
Ythdc1 C A 5: 86,975,961 (GRCm39) P529T possibly damaging Het
Zdhhc13 T C 7: 48,455,444 (GRCm39) probably null Het
Zfp282 A T 6: 47,882,023 (GRCm39) Y570F possibly damaging Het
Zfp872 A T 9: 22,111,407 (GRCm39) K295N probably damaging Het
Other mutations in Fbxo22
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4342:Fbxo22 UTSW 9 55,128,354 (GRCm39) splice site probably null
FR4737:Fbxo22 UTSW 9 55,116,666 (GRCm39) missense probably damaging 1.00
R0112:Fbxo22 UTSW 9 55,130,630 (GRCm39) missense probably benign 0.00
R0414:Fbxo22 UTSW 9 55,130,910 (GRCm39) missense possibly damaging 0.86
R0634:Fbxo22 UTSW 9 55,122,244 (GRCm39) missense probably benign 0.43
R0694:Fbxo22 UTSW 9 55,128,423 (GRCm39) missense probably damaging 0.99
R1799:Fbxo22 UTSW 9 55,130,771 (GRCm39) missense probably benign 0.00
R1958:Fbxo22 UTSW 9 55,116,626 (GRCm39) splice site probably null
R2060:Fbxo22 UTSW 9 55,125,667 (GRCm39) missense probably damaging 0.97
R2850:Fbxo22 UTSW 9 55,130,699 (GRCm39) missense probably damaging 1.00
R3883:Fbxo22 UTSW 9 55,130,546 (GRCm39) missense probably benign
R4649:Fbxo22 UTSW 9 55,128,333 (GRCm39) missense probably damaging 1.00
R5829:Fbxo22 UTSW 9 55,125,596 (GRCm39) splice site probably null
R7260:Fbxo22 UTSW 9 55,125,754 (GRCm39) missense probably benign 0.00
R7329:Fbxo22 UTSW 9 55,122,261 (GRCm39) missense probably benign 0.01
R7838:Fbxo22 UTSW 9 55,125,651 (GRCm39) missense probably damaging 1.00
R7921:Fbxo22 UTSW 9 55,125,637 (GRCm39) missense probably benign 0.18
R8313:Fbxo22 UTSW 9 55,128,344 (GRCm39) missense probably damaging 1.00
R9230:Fbxo22 UTSW 9 55,116,442 (GRCm39) missense probably damaging 1.00
R9401:Fbxo22 UTSW 9 55,130,628 (GRCm39) missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- ACCTCTGCTCTAAAAGATCAGTGAG -3'
(R):5'- CACAGGCATTCGTATAGGAGC -3'

Sequencing Primer
(F):5'- CTGCTCTAAAAGATCAGTGAGCTTTG -3'
(R):5'- TATAGGAGCAGTGCCCAAGTCTC -3'
Posted On 2020-09-02